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Thousand Oaks

511 ūüíľ Jobs / Employment in Thousand Oaks, CA

Associate Manufacturing - Thousand Oaks

new26 minutes ago
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This Cell Culture Manufacturing Associate position will support the re-commissioning and start-up of commercial cell culture drug substance intermediate manufacturing operations in Thousand Oaks, CA. The Sr. Associate will execute production operations on the manufacturing floor including execution and coordination of commissioning and qualification of process equipment. This role will interface between the GMP manufacturing teams in the plant and our partner organizations. Job scope and responsibilities: Execute set up, cleaning, sanitization, analytical testing, and manufacturing operations on the production floor. Ensure all safety and compliance procedures are followed at all times. Participate in the development, execution, and issue resolution associated with process equipment Commissioning, Qualification and Validation. Provide troubleshooting, technical support, and resolution of equipment, automation, and process issues on the manufacturing floor. Write and revise controlled documentation (SOPs, Manufacturing Procedures (MPs), Forms, Technical Reports, etc) Serve as SME for Cell Culture operations including cleanroom Aseptic Technique. Provide training to manufacturing staff on process and equipment. Implement Lean Transformation and OE initiatives, facilitate the drive towards continuous improvement in the plant, and track progress on a plant level. Collaborate with Quality, Engineering, Process Development, Validation, and Operations to resolve manufacturing events in a timely manner. Assure appropriate escalation to various levels of management when personnel and environmental safety, equipment functionality, product supply, or quality are at risk.Collaborate with Quality, Mfg Managers, Plant Engineering, Process Development and Regulatory Compliance staff in cross-functional teams. Apply advanced process, scientific, operational, and compliance knowledge with basic analytical and troubleshooting skills to support manufacturing operations. Participate in the design, development, and implementation of processes in support of the manufacturing floor.Basic Qualifications:Bachelor's degree OR Associates Degree and 4 years of biotech or pharmaceutical manufacturing, process development or quality experience OR High School Diploma / GED and 6 years of biotech or pharmaceutical manufacturing, process development or quality experience Preferred Qualifications:Available for non-standard shifts including nights and weekends. Degree in Chemical Engineering, Industrial Engineering or Life Sciences Technical understanding of drug substance intermediate (Cell Culture) operations Experience with Current Good Manufacturing Practices (cGMP) Ability to be flexible and manage change Experience participating in cross-functional teams Experience in managing multiple, competing priorities in a fast-paced environment Strong scientific, technical interactions with partner organizations such as PD and F&E. Experience in GMP Tech Support roles, GMP operations, process development or scheduling. Experience with execution of Commissioning and Qualification, New Product Introduction, Cleaning Validation, and Process Performance Qualification Experience with aseptic operations in Grade 5 (Class 100) cleanrooms. Technical knowledge of Upstream Drug Substance Intermediate processing and broad understanding of related disciplinary areas - Bioreactors, Roller Bottles, UFDF. Ability to organize, analyze, and interpret technical data through trend analysis, forecasting, modeling, etc. with excellent technical writing ability to convey processing events and conclusions Background in lean manufacturing methodologies and operational excellence Expertise in electronic systems used in manufacturing (MES/Werum, LIMS, Maximo, CCMS, etc.)Amgen focuses on areas of high unmet medical need and leverages its expertise to strive for solutions that improve health outcomes and dramatically improve people's lives. A biotechnology pioneer since 1980, Amgen has grown to be one of the world's leading independent biotechnology companies, has reached millions of patients around the world and is developing a pipeline of medicines with breakaway potential.We understand that to successfully sustain and grow as a global enterprise and deliver for patients - we must ensure a diverse and inclusive work environment. Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status. Join UsIf you're seeking a career where you can truly make a difference in the lives of others, a career where you can work at the absolute forefront of biotechnology with the top minds in the field, you'll find it at Amgen.Amgen, a biotechnology pioneer, discovers, develops and delivers innovative human therapeutics. Our medicines have helped millions of patients in the fight against cancer, kidney disease, rheumatoid arthritis and other serious illnesses.As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other but compete intensely to win. Together, we live the Amgen values as we continue advancing science to serve patients.Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.. Associated topics: biochemistry, bioengineering, biomaterials, biomedical, bioprocess, msat, neuro, neuroscience, pathogenesis, therapeutic

Hair Stylist - Thousand Oaks

newabout 1 hour ago
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Sport Clips is hiring Licensed Hairstylists, Cosmetologists and Barbers in our rapidly growing, exciting, fast-paced salonsJOB DESCRIPTIONSport Clips is the nation's leading Men's and Boys' hair care franchise, and we like to have FUN!!! Our salons are fully-equipped for the sports enthusiast by surrounding our Clients with televisions tuned to sports and sports-themed decor. Sport Clips is seeking Licensed Hair stylist/Cosmetologist and Barber who are passionate about making our Clients feel and look good. Join our team at Sport Clips as a Hair Stylist! Who doesnt LOVE working with a team of talented Hair Care Professionals in an energetic and supportive environment?BENEFITSBenefits of working with us include:Career opportunities.Manage a salonMentor Hair Stylists in your salonBe a part of the Sport Clips Ambassador TeamBecome a Technical Skills SpecialistBe a Coach (Educator)Work up to becoming a part of the Sport Clips traveling Artistic Team.Ongoing training provided by technical teams consisting of some of the best educators in the industry.Great pay including commissions paid on services and product sales, plus amazing tips!Strong marketing campaigns that increase clientele. No clientele needed.Flexibility for maintaining work-life balance and quality of life.JOB REQUIREMENTSCurrent cosmetology or barber license applicable to state requirements * Willing to work a flexible schedule * Ability to provide exceptional client service * Good communication skills * Strong work ethic * Ability to work in a Team atmosphere * Capable of performing administrative tasks such as completing transactions on the point of sale system, and light housekeeping dutiesTo apply, simply TEXT SPORTCLIPS to 25000 or visit here: http://oli.vi/NIzY7 and our virtual assistant Kenzie will get you scheduled for an interview today.Location Information:2072 E Avenida de Los ArbolesThousand Oaks, CA 91362

Hair Stylist - Thousand Oaks

newabout 1 hour ago
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Sport Clips is hiring Licensed Hairstylists, Cosmetologists and Barbers in our rapidly growing, exciting, fast-paced salonsJOB DESCRIPTIONSport Clips is the nation's leading Men's and Boys' hair care franchise, and we like to have FUN!!! Our salons are fully-equipped for the sports enthusiast by surrounding our Clients with televisions tuned to sports and sports-themed decor. Sport Clips is seeking Licensed Hair stylist/Cosmetologist and Barber who are passionate about making our Clients feel and look good. Join our team at Sport Clips as a Hair Stylist! Who doesnt LOVE working with a team of talented Hair Care Professionals in an energetic and supportive environment?BENEFITSBenefits of working with us include:Career opportunities.Manage a salonMentor Hair Stylists in your salonBe a part of the Sport Clips Ambassador TeamBecome a Technical Skills SpecialistBe a Coach (Educator)Work up to becoming a part of the Sport Clips traveling Artistic Team.Ongoing training provided by technical teams consisting of some of the best educators in the industry.Great pay including commissions paid on services and product sales, plus amazing tips!Strong marketing campaigns that increase clientele. No clientele needed.Flexibility for maintaining work-life balance and quality of life.JOB REQUIREMENTSCurrent cosmetology or barber license applicable to state requirements * Willing to work a flexible schedule * Ability to provide exceptional client service * Good communication skills * Strong work ethic * Ability to work in a Team atmosphere * Capable of performing administrative tasks such as completing transactions on the point of sale system, and light housekeeping dutiesTo apply, simply TEXT SPORTCLIPS to 25000 or visit here: http://oli.vi/NIzY7 and our virtual assistant Kenzie will get you scheduled for an interview today.Location Information:715 Wendy Dr.Newbury Park, CA 91320

Process Development Associate Scientist - Thousand Oaks

newabout 4 hours ago
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Amgen is currently seeking a Process Development Associate Scientist for our Pre-Pivotal Drug Product Technologies group in Thousand Oaks, CA. This group is responsible for early stage drug product formulation development for multiple modalities. Additionally, the position will develop novel formulations (liquid, lyophilized and frozen). The Associate Scientist will provide technical and project leadership while integrating information generated by cross functional teams to ensure success through the early stage drug product development process.Responsibilities include:Participate in the planning, design, execution, and documentation of laboratory studies related to formulation and fill/finish process development in support of product commercialization. Conduct stability studies, including preparation of formulations. This will involve knowledge of ultrafiltration-diafiltration and other buffer exchange processes. A solid understanding of lab scale sterile filling into vials and syringes will be needed. Execute development of protein drug formulations, analytical characterization of proteins, development of chromatographic and electrophoretic assays (UPLC/HPLC, SEC, CEX, RP-HPLC, CE-SDS and cIEF). Additional responsibilities include documenting and retrieving scientific results in HLEE notebooks and computer files for regulatory filings, participating in group and project meetings, and presenting at departmental seminars.Perform data analysis using advanced statistical/analytical techniques with statistical analysis software as needed.Author and review guideline documents, technical protocols, reports, and regulatory sections in support of IND application submissions.Deliver progress reports and presentations to ensure management awareness and engagement of the status, advancement, and future program functional needs within Operations.Ability to operate with principles of a safe laboratory environment.Basic Qualifications: Master's degree and 2 years of scientific experience OR Bachelor's degree and 4 years of scientific experiencePreferred Qualifications: Advanced degree in Biochemistry, Chemistry, Biomedical Engineering, Biotechnology, Pharmaceutics or related discipline with experience in pharmaceutical development and manufacturing Working experience with Protein Analytical methods: Solo VPEHPLC/UPLC, Capillary Electrophoresis, Particle analysis, Moisture analysis, Biophysical techniques such as CD and Fluorescence, Analytical centrifugation, light scattering (DLS, SLS). Should have fundamental knowledge of instrumental analysis, analytical chemistry and protein biochemistry. Proficient troubleshooting skills regarding laboratory analytical instruments. Strong teamwork, organizational skills, attention to detail and accuracy, excellent written and oral communication skills. Capable of quick learning and multitasking. Capable of learning a variety of computer software including software for electronic notebooks. Experience that includes elements of new product development, formulation development, process characterization, equipment design and implementation, Proven ability to learn and act on dynamic information at a rapid paceWe understand that to successfully sustain and grow as a global enterprise and deliver for patients - we must ensure a diverse and inclusive work environment.Amgen is committed to unlocking the potential of biology for patients suffering from serious illnesses by discovering, developing, manufacturing and delivering innovative human therapeutics. This approach begins by using tools like advanced human genetics to unravel the complexities of disease and understand the fundamentals of human biology.Amgen focuses on areas of high unmet medical need and leverages its expertise to strive for solutions that improve health outcomes and dramatically improve people's lives. A biotechnology pioneer since 1980, Amgen has grown to be one of the world's leading independent biotechnology companies, has reached millions of patients around the world and is developing a pipeline of medicines with breakaway potential. Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status. Join UsIf you're seeking a career where you can truly make a difference in the lives of others, a career where you can work at the absolute forefront of biotechnology with the top minds in the field, you'll find it at Amgen.Amgen, a biotechnology pioneer, discovers, develops and delivers innovative human therapeutics. Our medicines have helped millions of patients in the fight against cancer, kidney disease, rheumatoid arthritis and other serious illnesses.As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other but compete intensely to win. Together, we live the Amgen values as we continue advancing science to serve patients.Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.. Associated topics: aseptic technique, biopharma, clinical, dietetic, disease, food, histologist, pharmacy, protein, trauma

Pilot Plant - Manager, Downstream - Thousand Oaks

newabout 5 hours ago
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We are seeking a Manager for the Pilot Plant (based in Thousand Oak, CA) working in the Downstream team. This position will execute a variety of production-related operations in a large scale pilot plant, including but not limited to: performing processing on the floor (purification of Drug Substance); performing supporting activities such as buffer preparation, and equipment set-up/cleaning, execution of downstream operations, and managing staff. Work will also include executing production runs, experiments, commercial program support, and characterization efforts. Additional activities will include defining & documenting operation practices, ensuring documentation accurately reflects operations performed, developing and implementing area improvements (efficiency and safety) and lean principles, commissioning equipment, and participating in operations meetings.The Thousand Oaks Pilot Plant performs frequent piloting of novel process operations (focusing primarily on large molecule cell culture and purification operations), driving technology development, supporting innovation across Amgen's entire spectrum, as well as executing non-GMP and pre-pivotal GMP bioprocessing operations for multiple mammalian and microbial products in order to develop & demonstrate production processes and produce bulk material. We produce sound, relevant data for the processes Amgen developments at meaningful scales that enable the rapid, successful transfer of our output to more dedicated manufacturing spaces. The environment is challenging, fast-paced and ever-changing with varying degrees of process definition, but very rewarding for those that like hands-on science and want to make process improvements in a development space.Basic QualificationsDoctorate degree ORMaster's degree and 3 years of Manufacturing and Operations experience ORBachelor's degree and 5 years of Manufacturing and Operations experience ORAssociate's degree and 10 years of Manufacturing and Operations experience ORHigh school diploma / GED and 12 years of Manufacturing and Operations experience ANDPrevious managerial experience directly managing people and/or experience in leading teams, projects, programs or directing the allocation of resourcesPreferred QualificationsSolid knowledge of downstream, as well as a general knowledge of the associated analytical, and buffer preparation techniquesEnergetic and technically-minded, with strong interpersonal and organizational skillsDemonstrate the ability to learn new systems and applications, and various purification techniquesWork effectively in team and/or project environments; possess strong math and computer skills, as well as the ability to apply science-based thinking to practical applicationsExperience in cGMP production environmentBachelor's degree in Biology, Chemistry, or Chemical/Biological Engineering (or other relevant field) and 1or more years of managerial experience in Life Sciences fieldAmgen is committed to unlocking the potential of biology for patients suffering from serious illnesses by discovering, developing, manufacturing and delivering innovative human therapeutics. This approach begins by using tools like advanced human genetics to unravel the complexities of disease and understand the fundamentals of human biology.Amgen focuses on areas of high unmet medical need and leverages its expertise to strive for solutions that improve health outcomes and dramatically improve people's lives. A biotechnology pioneer since 1980, Amgen has grown to be one of the world's leading independent biotechnology companies, has reached millions of patients around the world and is developing a pipeline of medicines with breakaway potential. Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status. Join UsIf you're seeking a career where you can truly make a difference in the lives of others, a career where you can work at the absolute forefront of biotechnology with the top minds in the field, you'll find it at Amgen.Amgen, a biotechnology pioneer, discovers, develops and delivers innovative human therapeutics. Our medicines have helped millions of patients in the fight against cancer, kidney disease, rheumatoid arthritis and other serious illnesses.As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other but compete intensely to win. Together, we live the Amgen values as we continue advancing science to serve patients.Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.. Associated topics: fertilize, garden, lawn, manage, management, manufacture, plant, plant management, prune, ship

CNA - Certified Nursing Assistant - Thousand Oaks

newabout 5 hours ago
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Comfort Keepers Home Care, a World Leader, is hiring caregivers, homemakers, companions, CNAs and LVNs with a big heart and strong work ethic to provide non-medical care that helps seniors remain in their own homes and maintain full, independent lives. Our Comfort Keepers elevate the human spirit!Would you like to make a real difference in the life of a senior, working for a World Leader? Apply to be a Comfort Keeper!Comfort Keepers was voted as one of the TOP FOUR Employers in this area (Regional News site, 2018)!DUTIES We are looking for compassionate individuals to provide a range of services; including preparing basic meals, providing light housekeeping, laundry assistance, driving, dressing, grooming, fall prevention and companionship to our wonderful seniors. Some of our caregivers also provide mobility and personal hygiene assistance, but it is not a requirement of the job. REQUIREMENTS:You need to have caregiving experience, either paid or volunteer (like taking care of a loved one)OR Be a CNA or LVN (an expired license is okay!)You also need to have a dependable car that is your own to drive, a valid California Driver's License, valid car insurance, and be legally able to work in the United States.Our Comfort Keepers will also be LiveScan fingerprinted through the DOJ.Please live in the Ventura County, Conejo Valley, or West Valley areas Comfort Keepers is a World Leader, part of an international network of 700 officesComfort Keepers is the Ventura County Star READER'S CHOICE AWARD WINNER in 2014, 2015, 2016, 2017, and 2018 for Senior Services! BENEFITS TO YOU:* WE ARE EXTREMELY BUSY!* $100 Sign-On Bonus for current CNAs(easy conditions apply)* Healthcare Insurance for those who qualify- Medical, Dental, Vision * Flexible hours- Part-time, Full-time, Days, Afternoons, Nights, Overnights, and/or Weekends* Free In-Person Career Development Classes from our Comfort Keepers Learning Academy!* Mileage reimbursement* Amazing support team!* Monthly Caregiver Appreciation Days!* Excellent mentoring* Caregiver Learning Workshops - our Caregivers and CNA's love them!* Hundreds of free online career development / training classes* Paid sick leave* Higher pay rate for weekends, depending on your base rate* 10 Types of Bonuses* YOU CHOOSE WHICH CITIES YOU WOULD LIKE TO WORKWe service Camarillo, Ventura, Oxnard, Simi Valley, Moorpark, Newbury Park, Thousand Oaks, Westlake Village, Agoura Hills, West Hills, Calabasas, and surrounding citiesHOW DO I APPLY?BEST WAY is to apply online at:ckthousandoaks.clearcareonline.com/apply/OR come by our office to complete your online application8:45 AM to 4:00PM, Monday through Friday at3249 Old Conejo Rd.Newbury Park, CA 91320(805) ###-####Please be sure to check your voicemails and emails pretty often, so we can more easily connect with you. Thank you! We are also looking for caregivers!Great careers await you at Comfort Keepers! Associated topics: advanced, assistant cna, cardiology, certified nurse midwife, certified nursing, family nurse practioner, nurse specialist, practice, spanish, splst

Senior Associate Data Scientist - Thousand Oaks

newabout 6 hours ago
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Amgen is seeking a Senior Associate Data Scientist to be based in our Thousand Oaks, CA global headquarters, who will report to the head of Data Sciences for Digital Health & Innovation.To learn even more about Amgen's Data Science work, check out the recent Wired article on Amgen Data Science here. Digital Health & Innovation's mission is to position Amgen as the therapeutic leader of choice for patients through the discovery, development, and application of emerging digital solutions.The Senior Associate Data Scientist will be part of DH&I's Data Science team and will interface across Amgen's value chain in tackling important problems using cutting edge data science techniques. Your responsibilities would include executing on data science projects and providing technical input to projects involving data science, machine learning, and artificial intelligence across Amgen. Within the scope of these projects, our aim is to systematically integrate data, derive insights, generate predictions, and automate processes across the entire value chain in support of our mission and hence offers the opportunity for the candidate to collaborate with and learn from teams involved in Amgen processes ranging from R&D to Commercialization. Successful execution of these projects will not only demonstrate technical feasibility but will also derive substantial business value for Amgen. In this role you can expect to tackle extremely large and complex healthcare datasets, utilize cutting edge technologies and data science approaches, interact and learn from individuals all across Amgen, present your work in a variety of high profile settings, and most importantly contribute directly to Amgen's mission to serve patients.Primary Responsibilities for the Senior Associate Data Scientist include:Collaborating with other Data Scientists on the teamWorking closely with Product Innovation Leads and other Amgen Subject Matter Experts to best understand the business problemPerforming analyses and implementing machine learning solutions to address key business problemsCommunicating both verbally and in writing to both technical and non-technical audiences your work and its impactBasic Qualifications:Master's degreeORBachelor's degree and 2 years of Data Science experiencePreferred Qualifications:Experience with variety of data analysis and modeling methods particularly in their application to biological systems (i.e. Unsupervised (PCA, K-Means), Supervised (Linear/Logistic Regression, Deep Learning), Bayesian, Fourier/LaplaceProficient in SQL, Python, R and familiar with big data approachesFamiliarity and background with biotechnology processes and regulatory requirementsStrong analytical / quantitative skillsStrong communication and interpersonal skillsSelf-starter with the ability to take on several projects at one timeComfort and agility with changes in business prioritiesAmgen is committed to unlocking the potential of biology for patients suffering from serious illnesses by discovering, developing, manufacturing and delivering innovative human therapeutics. This approach begins by using tools like advanced human genetics to unravel the complexities of disease and understand the fundamentals of human biology.Amgen focuses on areas of high unmet medical need and leverages its expertise to strive for solutions that improve health outcomes and dramatically improve people's lives. A biotechnology pioneer since 1980, Amgen has grown to be one of the world's leading independent biotechnology companies, has reached millions of patients around the world and is developing a pipeline of medicines with breakaway potential.Join UsIf you're seeking a career where you can truly make a difference in the lives of others, a career where you can work at the absolute forefront of biotechnology with the top minds in the field, you'll find it at Amgen.Amgen, a biotechnology pioneer, discovers, develops and delivers innovative human therapeutics. Our medicines have helped millions of patients in the fight against cancer, kidney disease, rheumatoid arthritis and other serious illnesses.As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other but compete intensely to win. Together, we live the Amgen values as we continue advancing science to serve patients.Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.. Associated topics: clinical, cytometry, dietary, drug, health, immunology, industrial hygienist, medicine, protein, therapeutic

Undergrad Co-op - OPS (Pilot Plant) - Thousand Oaks, CA

newabout 7 hours ago
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Amgen discovers, develops and delivers innovative human therapeutics. A biotechnology pioneer since 1980, Amgen was one of the first companies to realize the new science's promise by bringing safe, effective medicines from lab, to manufacturing plant, to patient. Amgen therapeutics have changed the practice of medicine, helping millions of people around the world in the fight against cancer, kidney disease, rheumatoid arthritis, and other serious illnesses. With a deep and broad pipeline of potential new medicines, Amgen remains committed to advancing science to dramatically improve people's lives.We are seeking a co-op for the Thousand Oaks, CA Pilot Plant to execute a variety of production/related operations. The Co-op will perform both upstream and downstream process execution and support activities (such as vial thaw, cell culture, chromatography, filtration, centrifugation, UF/DF, buffer preparation and equipment setup/cleaning) and will be supporting technology development activities including characterization efforts. A significant amount of time will be spent performing hands-on work on the plant floor executing runs, performing experiments/studies and working with pilot scale equipment. This Pilot Plant performs bioprocessing operations for multiple mammalian products in order to develop and demonstrate production processes and to produce drug substance for a variety of purposes. The plant performs upstream and downstream production activities, from vial thaw through drug substance production. The environment is challenging and ever-changing, with varying degrees of process definition and frequent piloting of novel process operations.Relocation in the form of a miscellaneous allowance will be provided for eligible candidates.Basic Qualifications Amgen requires that all individuals applying for an undergraduate internship or an undergraduate co-op assignment at Amgen must meet the following criteria: 18 years or olderCurrently enrolled in a full time Bachelor's Degree program from an accredited college or university with a 3.0 minimum GPA or equivalentCompletion of one year of study from an accredited college or university prior to the internship commencingEnrolled in a full time Bachelor's degree program following the potential internship or co-op assignment with an accredited college or universityMust not be employed at the time the internship startsPreferred QualificationsDegree concentration in science and/or engineering (Biology, Chemistry, Chemical Engineering, etc.)Familiarity with MS Office (Word, Excel and PowerPoint)Previous Co-Op and/or academic lab experienceAbility to gown and gain entry to laboratory areasOnly candidates who apply via will be considered. Please search for Keyword 61334.#LI-DNIJoin UsIf you're seeking a career where you can truly make a difference in the lives of others, a career where you can work at the absolute forefront of biotechnology with the top minds in the field, you'll find it at Amgen.Amgen, a biotechnology pioneer, discovers, develops and delivers innovative human therapeutics. Our medicines have helped millions of patients in the fight against cancer, kidney disease, rheumatoid arthritis and other serious illnesses.As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other but compete intensely to win. Together, we live the Amgen values as we continue advancing science to serve patients.Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.. Associated topics: clinical, college of medicine, dietician, gastroenterology, medicine, mental, neuro, neurosurgery, nutrition, physician

Research Associate - CA - Thousand Oaks

newabout 8 hours ago
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Position Title: Research Associate - CA Location: Thousand Oaks, CA ZIP Code: 91320 Duration: 13months Contract with possible extension Shift: 8:00 am - 5:00 pm Mon-Fri Description: Minimum Basic Qualifications B.S. or M.S. degree in Analytical Chemistry, Physical, Life Sciences or related technical discipline. 4 years' experience performing analytical development and testing. Preferred Qualifications Master's degree in Analytical Chemistry, Physical or Pharmaceutical or Life Sciences or Engineering related discipline. Strong theoretical understanding, research in, and hands-on experience in small molecule/peptide analysis in support of process development/scale up activities and formulation development in GMP and non-GMP environments Additional experience in protein, protein conjugate analysis a plus Experience with a broad array of chromatographic (HPLC, GC, CE, SFC), spectroscopic techniques (FTIR, Raman, Mass spectrometry), dissolution development and testing, as well as associated electronic system (EMPOWER, eLN, Chrome Leon, etc.). Experience with process analytical techniques a plus (In-situ IR, Raman, FBRM) Demonstrate independence and ability to produce quality results under minimal direction Generate complete, accurate, and concise documentation using electronic systems and laboratory notebook High energy individual who can multi-task and handle a fast-pace, dynamic work environment Operate specialized laboratory equipment and instrumentation Perform general laboratory housekeeping activities Complete training on assigned tasks Comply with safety guidelines and site specific procedures which include but is not limited to, the maintenance of training records, laboratory documentation, written procedures, building monitoring systems and laboratory log books

Business System Analyst - Thousand Oaks

newabout 9 hours ago
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Amgen (NASDAQ:AMGN), a biotechnology pioneer, discovers, develops and delivers innovative human therapeutics. Our medicines have helped millions of patients in the fight against cancer, kidney disease, rheumatoid arthritis and other serious illnesses. With a deep and broad pipeline of potential new medicines, we continue to advance science to serve patients.Amgen is seeking an Information Systems, Specialist IS Business System Analyst located at its headquarters in Thousand Oaks, CA reporting to the Sr. Manager of Clinical Data Analysis IS services and primarily responsible for leading IS Services for three business capabilities: Statistical Study Design, Clinical Data Standards, and Clinical Data Statistical Analysis, and a shared SAS Analytical Platform Service. Collaborate with business partners and other IS service leads to define roadmap in support of business strategy and goals.Primary responsibilities may include: Leadership in defining technical and process improvements with many groups of business, IS and vendors to plan and implement City planning for future (ecosystem rationalization, cloud adoption, license negotiation, Cloud adoption, etc.) Leadership in driving innovative solution for Innovative Study Design by using new data science and machine learning Leadership to deliver innovative solution using R, Python, AWS, Databricks, and other latest technologies for Clinical Study Design Product ownership of enterprise class SAS Grid ecosystem used by thousands of users with global print spanning multiple department and external partners Accountable along with Amgen Service Providers to ensure 24x7 availability of mission critical applications Accountable to deliver IS service in alignment with business and IS strategy Interact with business clients, IS management and suppliers to lay out a technology roadmap, build business cases, manage projects to achieve the roadmap, and provide vendor oversight to manage system production activities Responsible for a variety of systems that support the business capabilities Partner with business and technology teams to elicit, analyze, translate, and document business requirements into technical requirements and solutions Responsible for managing key client relationships that are essential for the capability that this role will support Work directly with business partners to analyze current processes and capabilities to identify opportunities for improvements Manage vendor, service costs, requirements elicitation and documentation, market/vendor analysis, identification and management of risks Work closely with architects and technical SMEs, and enabling user adoptionBasic Qualifications:Doctorate degreeOR Master's degree and 2 years of Information Systems or Statistical Analysis experienceOR Bachelor's degree and 4 years of Information Systems or Statistical Analysis experienceOR Associate's degree AND 10 years of Information Systems or Statistical Analysis experienceORHigh school diploma/GED AND 12 years of Information Systems or Statistical Analysis experiencePreferred Qualifications: Good understanding of Artificial intelligence and data science Good understanding of full stack development and DevOps Experience developing multiyear technology plan Understand business functionality and translate it into application requirements Ability to create compelling business cases with accurate cost and effort estimations Excellent understanding of business complexity and project interdependencies Intellectual curiosity and the ability to question thought partners across functional areas Outstanding written and verbal communication skills Ability to explain complex technical concepts to non-technical clients Analytical skills and techniques to evaluate interpret and resolve complex situations/problems using multiple sources of information Knowledge of SAS GRID architecture, Real world data, Clinical trial data, and analytics and visualization solutions Familiar with SAS, R, Python programming Familiar with AWS architecture and Databricks Understanding of SDLC (System Development Life Cycle) methodologies Experience in biotechnology or other healthcare environment Sharp learning agility, problem solving and analytical thinking Ability to lead and influence clients, other business analysts, and technical team members Experience delivering solutions in a managed service delivery model Experience managing regulated systemsAmgen is committed to unlocking the potential of biology for patients suffering from serious illnesses by discovering, developing, manufacturing and delivering innovative human therapeutics. This approach begins by using tools like advanced human genetics to unravel the complexities of disease and understand the fundamentals of human biology.Amgen focuses on areas of high unmet medical need and leverages its expertise to strive for solutions that improve health outcomes and dramatically improve people's lives. A biotechnology pioneer since 1980, Amgen has grown to be one of the world's leading independent biotechnology companies, has reached millions of patients around the world and is developing a pipeline of medicines with breakaway potential.Join UsIf you're seeking a career where you can truly make a difference in the lives of others, a career where you can work at the absolute forefront of biotechnology with the top minds in the field, you'll find it at Amgen.Amgen, a biotechnology pioneer, discovers, develops and delivers innovative human therapeutics. Our medicines have helped millions of patients in the fight against cancer, kidney disease, rheumatoid arthritis and other serious illnesses.As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other but compete intensely to win. Together, we live the Amgen values as we continue advancing science to serve patients.Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.. Associated topics: analysis, bi, business analytic, business intelligence, financial reporting analyst, investment banking, investment fund, market, refinement, strategy

Director, Modeling and SImulation - Thousand Oaks

newabout 10 hours ago
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Amgen is a values based organization with a powerful sense of shared purpose toward our mission: to serve patients. We encourage our team members to have fulfilling and meaningful careers through challenging assignments, career development, and valuable opportunities such as this.Biotechnology opened the door to new types of medicines based on nature's own building blocks. No company has done more to advance this revolution than Amgen & the company's broad toolkit of drug modalities just got larger www.amgenscience.com/the-shape-of-drugs-to-come . The Clinical Pharmacology, Modeling & Simulation Department at Amgen (Thousand Oaks, CA) is seeking a Director, Modeling and Simulation.Responsibilities:The Director will be responsible for the development and implementation of the modeling and simulation strategies and execution of tasks for clinical development candidates across multiple novel modalities including T-cell engagers and cellular therapies in addition to monoclonal antibodies and small molecules. Key responsibilities include leading a team of modelers responsible across multiple indications in the oncology therapeutic area for:Conducting PK/PD and exposure-response analyses of data from early to late phase clinical studies using pharmacostatistical and relevant state of the art modeling and simulation techniquesPerforming meta-analysis using proprietary and/or literature dataParticipating in cross-functional project teams and providing scientific input for dose selection for early and late stage clinical study designs using quantitative methodsContributing to clinical pharmacology plans by establishing and implementing high impact modeling and simulation strategy for clinical development candidatesAuthoring PK/PD reports and contributing to summary documents for regulatory submissions.Basic Qualifications:Doctorate degree and 4 years of Modeling & Simulation scientist in the Biotechnology/ Pharmaceutical IndustryORMaster's degree and 7 years of Modeling & Simulation scientist in the Biotechnology/ Pharmaceutical IndustryORBachelor's degree and 9 years of Modeling & Simulation scientist in the Biotechnology/ Pharmaceutical IndustryPreferred Qualifications:PhD in applied (bio)statistics, (bio)engineering, applied biomathematics/biophysics or related fields with equivalent professional degrees10 years of experience as Modeling & Simulation scientist in the Biotechnology/ Pharmaceutical Industry.Experience mentoring and supervising junior modelersDeep understanding of clinical pharmacology and early and late phase clinical developmentExpertise and past hands-on experience analyzing pharmacokinetic, efficacy and safety data from clinical trials using advanced pharmacometric or statistical modeling methodologies and conducting clinical trial simulations to assist study designExpertise in standard pharmacometric software (e.g. NONMEM, R, SAS, MATLAB) and programming languagesExpertise in binary and categorical data analyses, time-to-event (hazard) models, Poisson models, logistic regression, MCMC and Bayesian methods as applied to exposure-response analyses, meta-analyses and Population PK and PKPD analysisExpert knowledge in developing modeling analysis plans, population PKDPD and translational modeling strategies, developing clinical study designs and dose optimizationTrack record of regulatory filings (NDA/BLA) and responding to regulatory agency questions and knowledge of global regulatory requirements and guidances on quantitative analysesExperience guiding the development/maintenance pharmacometric infrastructure, justifying and implementing innovative pharmacometric software/tools, leading innovative methodology/algorithm development for modeling and simulations, and organizing trainings and educations to embrace cutting-edge technologies in pharmacometricsExperience recognizing and anticipating discovery/translation/development problems that can be addressed by applying quantitative methods and finding effective solutions in partnership and collaboration with cross-functional teams to enable decision-making. Track record of influencing a broad spectrum of stakeholders toward achieving business goalsExcellent interpersonal, verbal and written communication skills and the ability to function in a highly matrixed team environment are essential.Previous record of scientific contributions through peer-reviewed articles and external presentationsOur culture is what makes Amgen a special place to work. We have a powerful shared purpose around our mission - to serve patients. We respect one another, recognize contributions, and have embedded collaboration, trust, empowerment and inclusion in all that we do.Amgen is committed to unlocking the potential of biology for patients suffering from serious illnesses by discovering, developing, manufacturing and delivering innovative human therapeutics. This approach begins by using tools like advanced human genetics to unravel the complexities of disease and understand the fundamentals of human biology.Amgen focuses on areas of high unmet medical need and leverages its expertise to strive for solutions that improve health outcomes and dramatically improve people's lives. A biotechnology pioneer since 1980, Amgen has grown to be one of the world's leading independent biotechnology companies, has reached millions of patients around the world and is developing a pipeline of medicines with breakaway potential.#LI-POSTJoin UsIf you're seeking a career where you can truly make a difference in the lives of others, a career where you can work at the absolute forefront of biotechnology with the top minds in the field, you'll find it at Amgen.Amgen, a biotechnology pioneer, discovers, develops and delivers innovative human therapeutics. Our medicines have helped millions of patients in the fight against cancer, kidney disease, rheumatoid arthritis and other serious illnesses.As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other but compete intensely to win. Together, we live the Amgen values as we continue advancing science to serve patients.Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.. Associated topics: biological engineer, biology, biomaterials, biomedical, biomedical engineer, bioprocessing, enzyme, neurodegenerative, nutrition, therapeutic

Scientist - Protein Engineering & Display - Thousand Oaks

newabout 12 hours ago
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Biologics Optimization is seeking a highly motivated Scientist to join the Biologics Combinatorial Engineering Team at our state-of-the-art research facility at the Amgen headquarters in Thousand Oaks, CA. The Biologics Optimization department is responsible for the design, optimization, production, assessment, and selection of large therapeutic drug candidates.The Biologics Combinatorial Engineering Team is responsible for the affinity modulation and optimization of antibody and protein therapeutics. The Scientist will be a part of a multidisciplinary team with capabilities in protein engineering, yeast display, cloning, expression, purification and characterization of large molecule drug candidates.Responsibilities:Design and execute display selection strategies addressing the protein engineering problems of complex biologic molecules.Act as a scientific leader with the ability to drive innovation, lead projects and teams, solve complex technical problems, work independently and in cross-functional teams.Develop and implement innovative technologies to improve efficiency and speed of the processes in the Biologics Optimization organization.Provide scientific results that support the generation of publications, patents, or regulatory submissions, and participate in internal and external scientific meetings.Basic Qualifications:Doctorate degreeORMaster's degree and 4 years of scientific experienceORBachelor's degree and 6 years of scientific experiencePreferred Qualifications:A strong track record of research accomplishments in protein engineering.Experience in laboratory display techniques (yeast or mammalian), FACS, and molecular cloning.Familiar with automation platforms and/or structural modeling programs such as Pymol, MOE, Schrodinger, or Rosetta.Understanding of protein biophysical and biochemical properties that relate to molecule activity and stability.Strong communication and interpersonal skills, and the ability to work flexibly in a dynamic and collaborative environment.A strong track record of independent critical thinking and scientific achievement in research, exemplified by publications in highly regarded journals, conference presentations or generation of intellectual propertyOur culture is what makes Amgen a special place to work. We have a powerful shared purpose around our mission - to serve patients. We respect one another, recognize contributions, and have embedded collaboration, trust, empowerment and inclusion in all that we do.Join UsIf you're seeking a career where you can truly make a difference in the lives of others, a career where you can work at the absolute forefront of biotechnology with the top minds in the field, you'll find it at Amgen.Amgen, a biotechnology pioneer, discovers, develops and delivers innovative human therapeutics. Our medicines have helped millions of patients in the fight against cancer, kidney disease, rheumatoid arthritis and other serious illnesses.As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other but compete intensely to win. Together, we live the Amgen values as we continue advancing science to serve patients.Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.. Associated topics: biological engineer, biomechanics, biophysics, enzyme, fermentation, medical, neurodegenerative, nutrition, pathogenesis, therapeutic

Regulatory Affairs Manager (US) - Thousand Oaks

newabout 15 hours ago
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Amgen is searching for a Regulatory Affairs Manager to work in our Global Regulatory Affairs group. This Manager will report to the Director Regulatory Affairs and will work out of our main corporate campus in Thousand Oaks, CA. This Manager will support one or more products from a regional regulatory perspective. As a member of the Global Regulatory Team (GRT), the Manager will achieve the desired labeling by developing and executing regional regulatory strategies and managing effective agency interactions.Responsibilities for the Regulatory Affairs Manager include:Ensure that Amgen acquires and maintains all the licenses in order to support clinical trials for investigational medicinal products as well as market commercially approved medicinal products.Ensure regulatory compliance, with a focus on patient safety.Provide management and leadership by supervising one or more other regional regulatory leads and/or support staff.Execute the approved regional strategy for assigned programs.Advise the Global Regulatory Team (GRT) on regional considerations in developing strategy.Ensure the regional needs are well defined and implemented in collaboration with relevant regional stakeholders.Plan and manage regulatory submissions (e.g. clinical trial and marketing applications) for products within Amgen's portfolio in compliance with global filing plans and local regulatory requirements.Under general supervision, implement product related regulatory strategies, Regulatory Affairs processes and activity planning in accordance with national legislation and regulatory requirements.Provide content guidance for regional regulatory documents and meetings in accordance with GRT strategy.Provide regulatory guidance on regional regulatory mechanisms to optimize product development (e.g. expediting FIH studies, Orphan Drug, Fast Track, compassionate use and pediatric plan).Manage the development of the regional product label by collaborating with the Labeling Working Group to define commercial objectives in the context of available and expected scientific data, regulatory guidance and precedent.Support regional label negotiation activities.Under general supervision participate in the development, and execution of regional regulatory product strategies, including precedence, risk management and contingency planning.Consistent with GRT strategy, advise GDT on regulatory implications and requirements related to global clinical development plans and objectivesObtain and maintain Clinical Trial Authorizations and Marketing Application approvals including Response to Questions (RTQs)Communicate regulatory strategies within team (e.g. GRT, local affiliates).Under general supervision, develop predictions for expectations and risks associated with outcomes by regulatory agencies.Ensure regulatory product compliance for product (e.g. IMR, PMCs, pediatric and other agency commitments).Communicate and ensure alignment of regional management before GRT strategy decisions.Partner with regional management and peers to ensure consistency in procedures and agency interactions.Maintain an awareness of new and developing legislation, regulatory policy and technical Regulatory guidance relating to Amgen products.Perform regulatory research to obtain relevant histories, precedence and other information relevant to regional product advancement.Basic Qualifications:Doctorate DegreeORMaster's Degree & 3 years of Regulatory experienceORBachelor's Degree & 5 years of Regulatory experienceORAssociate's degree & 10 years of Regulatory experienceORHigh school diploma/GED & 12 years of Regulatory experiencePreferred Qualifications:Regulatory submissions experienceExperience interacting with regulatory agenciesClinical Development experienceCross-functional experience Knowledge and SkillsRegulatory principlesWorking with policies, procedures and SOP'sKnowledge of national legislation and regulations relating to medicinal productsAwareness of the registration procedures in region for MA, post approval changes, extensions and renewalsKnowledge of drug development Scientific / Technical ExcellenceCommunication skills - both oral and writtenAbility to understand and communicate scientific/clinical informationAbility to anticipate and prevent potential issuesKnowledge of and experience in regional regulatory environment in relevant product area and development stageUnderstanding of regulatory activities and their touch pointsAbility to resolve conflicts and develop a course of action leading to a beneficial outcomeCultural awareness and sensitivity to achieve results across both regional country and International bordersAmgen is committed to unlocking the potential of biology for patients suffering from serious illnesses by discovering, developing, manufacturing and delivering innovative human therapeutics. This approach begins by using tools like advanced human genetics to unravel the complexities of disease and understand the fundamentals of human biology.Amgen focuses on areas of high unmet medical need and leverages its expertise to strive for solutions that improve health outcomes and dramatically improve people's lives. A biotechnology pioneer since 1980, Amgen has grown to be one of the world's leading independent biotechnology companies, has reached millions of patients around the world and is developing a pipeline of medicines with breakaway potential.Join UsIf you're seeking a career where you can truly make a difference in the lives of others, a career where you can work at the absolute forefront of biotechnology with the top minds in the field, you'll find it at Amgen.Amgen, a biotechnology pioneer, discovers, develops and delivers innovative human therapeutics. Our medicines have helped millions of patients in the fight against cancer, kidney disease, rheumatoid arthritis and other serious illnesses.As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other but compete intensely to win. Together, we live the Amgen values as we continue advancing science to serve patients.Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status..

Associate Scientist - Process Development - Thousand Oaks

newabout 15 hours ago
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Amgen is currently seeking an Associate Scientist in our Pivotal Drug Product Technologies Group in Thousand Oaks, CA. The Associate Scientist will be responsible for performing formulation and process characterization studies, evaluating the impact of process stresses on Drug Product attributes and stability, as well as process parameter definition for various fill finish unit operations. In addition, to laboratory-based work, the ideal candidate will have also demonstrated a strong interest in developing and applying data analytics to their work.Responsibilities include: Participate in the planning, design, execution, and documentation of studies related to drug product design, formulation development, and process development in support of commercialization and life cycle management of various modality biologics (antibody, BiTE, other proteins, viruses, RNA). Perform analytical characterization supporting formulation attribute and stability assessments using chromatography and biophysical characterization tools (SE-HPLC, CE-SDS, DSC, NMR, HIAC). Author and review technical protocols, reports, product impact assessments, and regulatory sections in support of IND and marketing application submissions. Actively utilize advanced IS systems to improve drug product design through faster data availability, leveraging historical information, analyzing large data sets, and statistical analysis. Create visualizations to enable business application of data analysis. Explore and evaluate new digital tools and techniques to improve the team's developmental and operational capabilities As needed, provide support to clinical and commercial fill/finish manufacturing operations through process capability analysis, troubleshooting, root cause analysis, and product impact assessments for non-conformance investigations and process changes/improvements. Support standardization and optimization of departmental practices by contributing to guideline documents Deliver timely updates and presentations to project teams and leadership. Ability to travel domestically and internationally up to 10% of the time.Basic Qualifications: Master's degree and 2 years of scientific experience OR Bachelor's degree and 4 years of scientific experiencePreferred Qualifications: Master's degree in Pharmaceutics, Biotechnology, Engineering, Material Science or related discipline 4 years of experience in pharmaceuticals/biotechnology that includes elements of new product development, process characterization, formulation development, equipment design and implementation, technology transfers, statistical process control (SPC), and statistical design and analysis of experiments Experience with characterization of drug product formation and fill/finish unit operations (i.e. freeze/thaw, formulation, mixing, filtration, filling, and inspection) Understanding of physical/chemical stability of proteins and how process related stress impacts molecule attributes and product quality In addition to proteins, experience with alternate modalities (RNA or live modalities) is a plus Proficiency with statistical analyses (using software such as SIMCA, JMP, SPSS) Experience with data visualization tools or packages, such as Tableau or Spotfire Experience with coding/scripting for automated data analysis and modeling to enable better access and standardization across the function Aseptic processing experience and familiarity with cGMPs Regulatory filings and compliance issues for sterile injectable products Strong problem solving and effective cross-functional communication skills Proven ability to learn and act on dynamic information at a rapid paceWe understand that to successfully sustain and grow as a global enterprise and deliver for patients - we must ensure a diverse and inclusive work environment.Amgen is committed to unlocking the potential of biology for patients suffering from serious illnesses by discovering, developing, manufacturing and delivering innovative human therapeutics. This approach begins by using tools like advanced human genetics to unravel the complexities of disease and understand the fundamentals of human biology.Amgen focuses on areas of high unmet medical need and leverages its expertise to strive for solutions that improve health outcomes and dramatically improve people's lives. A biotechnology pioneer since 1980, Amgen has grown to be one of the world's leading independent biotechnology companies, has reached millions of patients around the world and is developing a pipeline of medicines with breakaway potential.Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.Join UsIf you're seeking a career where you can truly make a difference in the lives of others, a career where you can work at the absolute forefront of biotechnology with the top minds in the field, you'll find it at Amgen.Amgen, a biotechnology pioneer, discovers, develops and delivers innovative human therapeutics. Our medicines have helped millions of patients in the fight against cancer, kidney disease, rheumatoid arthritis and other serious illnesses.As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other but compete intensely to win. Together, we live the Amgen values as we continue advancing science to serve patients.Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.. Associated topics: bacteria, clinical, drug discovery, immunohematology, kinesiology, medical, medicine, physiology, therapy, virus

Medical Writer - Thousand Oaks

newabout 16 hours ago
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Job Description We are searching for a Global Publications - Manager to join the Oncology Therapeutic Area (TA) team in Thousand Oaks, CA, reporting to a group leader in Global Publications. The successful candidate will work with cross-functional and cross-regional leaders to develop high impact Publications aligned with program objectives for Oncology marketed products and pipeline molecules. Additional responsibilities include the following: Align with key stakeholders (e.g. clinical development, global medical affairs) for the development of the publications Medical writing and/or manage publication Manage publication development timelines and execution of abstracts, posters, oral presentations, and manuscripts Influences the global publication planning team and author decisions based on experience and knowledge of publication landscape (eg, selection of appropriate journal or congress) Ensure compliance with [Comapany] publication policy and external publication guidelines Critically review publications Clinical support of key scientific congresses and meetings Some travel required; occasionally up to 10%. Basic Qualifications Doctorate degree & 0-2 years of directly related experience OR Master s degree & 6 years of directly related experience OR Bachelor s degree & 8 years of directly related experience Preferred Qualifications PhD, MD, PharmD, with 1-2 years of Clinical Development/Medical Affairs/Regulatory experience in the area of Oncology clinical and therapeutic issues Current or previous medical writing experience (in pharma and/or agency) Aptitude in writing and presenting on scientific and clinical issues. Excellent communication (written and verbal), interpersonal, organizational, time management, and project management/planning skills Experience developing content across different therapeutic areas or for diverse audiences (discovery research, clinical development, global health economics, observation research, etc) Associated topics: ancmg, aoa, breast, hem onc, lah, oncology, palliative, physician md, physician md do, thedacare

Undergrad Co-op - OPS (Pilot Plant) - Thousand Oaks, CA

newabout 19 hours ago
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Amgen discovers, develops and delivers innovative human therapeutics. A biotechnology pioneer since 1980, Amgen was one of the first companies to realize the new science's promise by bringing safe, effective medicines from lab, to manufacturing plant, to patient. Amgen therapeutics have changed the practice of medicine, helping millions of people around the world in the fight against cancer, kidney disease, rheumatoid arthritis, and other serious illnesses. With a deep and broad pipeline of potential new medicines, Amgen remains committed to advancing science to dramatically improve people's lives.We are seeking a co-op for the Thousand Oaks, CA Pilot Plant to execute a variety of production/related operations. The Co-op will perform both upstream and downstream process execution and support activities (such as vial thaw, cell culture, chromatography, filtration, centrifugation, UF/DF, buffer preparation and equipment setup/cleaning) and will be supporting technology development activities including characterization efforts. A significant amount of time will be spent performing hands-on work on the plant floor executing runs, performing experiments/studies and working with pilot scale equipment. This Pilot Plant performs bioprocessing operations for multiple mammalian products in order to develop and demonstrate production processes and to produce drug substance for a variety of purposes. The plant performs upstream and downstream production activities, from vial thaw through drug substance production. The environment is challenging and ever-changing, with varying degrees of process definition and frequent piloting of novel process operations.Relocation in the form of a miscellaneous allowance will be provided for eligible candidates.Basic Qualifications Amgen requires that all individuals applying for an undergraduate internship or an undergraduate co-op assignment at Amgen must meet the following criteria: 18 years or olderCurrently enrolled in a full time Bachelor's Degree program from an accredited college or university with a 3.0 minimum GPA or equivalentCompletion of one year of study from an accredited college or university prior to the internship commencingEnrolled in a full time Bachelor's degree program following the potential internship or co-op assignment with an accredited college or universityMust not be employed at the time the internship startsPreferred QualificationsDegree concentration in science and/or engineering (Biology, Chemistry, Chemical Engineering, etc.)Familiarity with MS Office (Word, Excel and PowerPoint)Previous Co-Op and/or academic lab experienceAbility to gown and gain entry to laboratory areasOnly candidates who apply via will be considered. Please search for Keyword 61334.#LI-DNIJoin UsIf you're seeking a career where you can truly make a difference in the lives of others, a career where you can work at the absolute forefront of biotechnology with the top minds in the field, you'll find it at Amgen.Amgen, a biotechnology pioneer, discovers, develops and delivers innovative human therapeutics. Our medicines have helped millions of patients in the fight against cancer, kidney disease, rheumatoid arthritis and other serious illnesses.As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other but compete intensely to win. Together, we live the Amgen values as we continue advancing science to serve patients.Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.. Associated topics: behavioral science, cardiology, clinical, dietician, genetic, health care, human disease, instructor md, medicine, otolaryngology

PCU RN Progressive Care Unit Travel ( Thousand Oaks , CA )

newabout 19 hours ago
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PCU RN, Progressive Care Unit Travel Registered Nurse Jobs & Assignments Looking for a PCU travel assignment? You are in the right place, the HCEN Network of staffing

jobs byJuju.com

Seasonal Travel RN - ICU, ED, Or, PACU ( Thousand Oaks , CA ) - HealthCare Traveler Jobs

newabout 19 hours ago
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Critical Need for All Hospital Based RN Specialties Travel Registered Nurse Jobs & Assignments Would you like to spend the spring / summer somewhere great? The

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HealthCare Traveler RN, Critical Care Specialties ( Thousand Oaks , CA ) - HealthCare Traveler Jobs

newabout 19 hours ago
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Critical Need for All Hospital Based RN Specialties Travel Registered Nurse Jobs & Assignments Looking for an RN travel assignment? You are in the right place, the

jobs byJuju.com

Observational Research Manager - Thousand Oaks

newabout 20 hours ago
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Amgen is searching for an Observational Research Manager (Epidemiology) | Job # 66679. This manager will have responsibilities for research activities in the the Non-Oncology or Oncology therapeutic area (TA) and reports directly to a Therapeutic Area Director. This role can be located on the Amgen corporate campus in Thousand Oaks, CA. A remote working arrangement can be considered as well. Observational Research (OR) makes important contributions to drug development, commercialization, and safety evaluation. Observational Research contributes evidence regarding the frequency and distribution of disease, the natural history and clinical burden of disease, the design of clinical trials, cost and utilization patterns, and the safety and effectiveness of therapies. There is increasing demand for information from OR studies by regulatory and reimbursement authorities. The Center for Observational Research (CfOR) was created to address this imperative.A CfOR Manager is recognized as a strong scientific contributor and is a first or contributing author for papers in peer reviewed journals or for internal reports that enhance the company's mission.Key Activities include:Contributes to research strategy within the product teams and observational research TAExecutes or manages descriptive epidemiologic studies to characterize the incidence/prevalence of disease in US, EU, Asia, and emerging market countriesExecutes or manages research projects involving the analysis of multiple types of data including medical claims, EMR, and prospective observational cohort studiesExecutes pharmacovigilance studiesProvides safety research support across the life cycle of Amgen productsSupports development of risk management plansConducts literature reviews and prepares research reports and scientific manuscriptsStays abreast of the latest developments in the field of observational research and drug developmentPromotes awareness, understanding, and use of observational research methodsSupports relationships with key leaders in observational researchProvides input into observational research department meetingsCommunicates significant scientific information to a variety of audiences#LI--POSTBasic Qualifications:Doctorate degreeORMaster's degree and 3 years of scientific experienceORBachelor's Degree and 5 years of scientific experienceORAssociate's degree and 10 years of scientific experienceORHigh school diploma / GED & 12 years of scientific experiencePreferred Qualifications:Doctorate in Epidemiology or other subject with high observational research contentExperience in the design, execution, and analysis of observation research studies within Pharmaceutical or Public Health settingExperience in research to support drug developmentExperience in observational research project planning and managementExperience communicating observational research information (written and oral)Experience working in multi-disciplinary teamsRecord of publications in observational research or clinical journalsOur culture is what makes Amgen a special place to work. We have a powerful shared purpose around our mission - to serve patients. We respect one another, recognize contributions, and have embedded collaboration, trust, empowerment and inclusion in all that we do.Amgen focuses on areas of high unmet medical need and leverages its expertise to strive for solutions that improve health outcomes and dramatically improve people's lives. A biotechnology pioneer since 1980, Amgen has grown to be one of the world's leading independent biotechnology companies, has reached millions of patients around the world and is developing a pipeline of medicines with breakaway potential.Be behind world-renowned products and services. With our industry reputation and strong product pipeline, you can take pride in working at Amgen.Join UsIf you're seeking a career where you can truly make a difference in the lives of others, a career where you can work at the absolute forefront of biotechnology with the top minds in the field, you'll find it at Amgen.Amgen, a biotechnology pioneer, discovers, develops and delivers innovative human therapeutics. Our medicines have helped millions of patients in the fight against cancer, kidney disease, rheumatoid arthritis and other serious illnesses.As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other but compete intensely to win. Together, we live the Amgen values as we continue advancing science to serve patients.Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.. Associated topics: aseptic, drug discovery, immunology, industrial hygienist, injury, microbiological, pharmacometrics, protein, toxicologist, transfection

NEURO Professional Sales Representative, Thousand Oaks, CA - Assertio Therapeutics

newabout 22 hours ago
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The Professional Sales Representative is responsible for implementing marketing strategy by delivering proficient sales presentations to a defined list of current and prospective customers. In the assigned territory, the Sales Specialist will utilize all marketing and selling materials designed for a respective audience. Customers include, but are not limited to physicians, healthcare providers, retail/wholesale accounts, and hospitals/clinics. Essential Functions Creates product demand by effectively executing marketing strategy Develops and implements robust territory business plans centered on performance; meet or exceed territory productivity requirements Conducts an assertive selling approach with customers combining individualized selling methods with approved marketing tools. Demonstrates high-level proficiency in utilizing business data and analysis to set a clear course of actionExpert in creating a long-term plan for enhancing customer relationship and leveraging managed care opportunity Effectively leverages Specialty Pharmacies to drive sales results Demonstrates high level skill in developing and working with Regional/Local KOLs Demonstrates account management sales execution based on creating product value to the prescriber, which includes customer satisfaction and rigorous application of company resources Demonstrates highly effective territory management and superior selling competencies Demontrates sales strategy in linking each call to the next call to the entire call continuum with immediate follow up on pending issues Demonstrates the ability of developing self to drive and enhance performanceFosters team effectiveness and accomplishments by sharing knowledge, experience and information. Represent products in a professional, compliant, ethical and effective manner Effective management of territory resources and budgetRequirementsEducation/Experience: Bachelor's degree (Majors preferred - Sciences, Business, Healthcare Fields Minimum of 2 years of strong B2B and/or previous Pharma sales, biotech sales or medical device sales, including strong results-oriented technical sales experience. Experience preferred in the areas of Pain Management and Neurology. Proficiency in Excel, Word, Outlook, and database applications. Ability to travel (may include overnight travel).Should reside in territory geography or be willing to relocate. Valid Driver's License and an acceptable driving record. Authorization and ability to drive a Company leased vehicle or authorized rental vehicle. Physical Requirements:Ability to operate a motor vehicle Ability to travel via airplane Ability to sit for long periods of time Ability to have close visual acuity to perform an activity such as: preparing and analyzing data and figures; transcribing; viewing a computer terminal. Reaching: Extending hand(s) and arm(s) in any direction. Standing: Remaining upright on the feet. Pushing: Using upper extremities to press against something with steady force in order to thrust Lifting: Raising objects from a lower to a higher position or moving objects horizontally from position-to-position of up to 20 lbs. on occasion Mental Requirements Ability to prepare and analyze data and figures Ability to understand, remember and apply oral and written instructions Ability to organize and prioritize own works schedule Ability to apply common sense in performing job Ability to understand and follow instructionsAbout UsTHE COMPANYAssertio Therapeutic is a leading specialty pharmaceutical company committed to putting the Patient First in everything we do; with a focus on enhancing the lives of patients, families, physicians, providers and in payors through commercialization of products in the areas of neurology, orphan and specialty therapies.Assertio has a clear THREE PILLAR strategy for growth:MAINTAIN a strong/profitable NUCYNTA franchise through a commercialization agreement with Collegium, GROW the Neurology Business and BUILD a new Specialty Business through a recent Cosyntropin transaction. The company's strategy is to continue to identify, license and develop new products-that offer enhanced therapeutic options to patient populations that may be underserved by existing therapies.Assertio is an AA/EEO/Veterans/Disabled employer. Associated topics: director of sales, management, manager, principal, sales director, sales executive, sales manager, shift lead, supervisor, team leader

Principal Reference Data Engineer - Thousand Oaks

new1 day ago
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Principal Reference Data EngineerAmgen (NASDAQ:AMGN), a biotechnology pioneer, discovers, develops and delivers innovative human therapeutics. Our medicines have helped millions of patients in the fight against cancer, kidney disease, rheumatoid arthritis and other serious illnesses.The Principal Reference Data Engineer will be part of the Enterprise Engineering and Analytics (EEU) organization and will be accountable for solution delivery and adoption of Amgen's Reference Data Platform and Semantic technologies. This role is based in Thousand Oaks, CA. This role will be responsible for partnering with the business and client-facing IS groups for creation of vocabularies/ taxonomies/ontologies, promoting the use of the reference data platform, developing analytic solutions using semantic technologies, mentoring and advancing a team of junior ontologists, owning & managing the roadmap for enterprise reference data platform, and driving adoption.Responsibilities: Work with Business and Client-facing IS groups to model and develop vocabularies/taxonomies/ontologies for specific applications and use cases.Onboard public-domain ontologies to Reference data platform (Semaphore).Remodel reference data content for improved reusability, scalability, and maintainability to support increased adoption.Provide architectural direction and recommend design pattern to projects planning on integration with Reference data platform for consuming terminologies (from reference data platform and/or reference data hub).Responsible for reference data platform ownership in CMDB and managing the roadmap for reference data platform.Responsible for the RunOps of Reference data platform and reference data hub.Responsible for communicating the roadmap and value of reference data platform to senior management across IS and business.Develop training, roadshow materials, and outreach events (e.g. reference data symposium) to increase the adoption of reference data platform.Work with Business and Client-facing IS to develop analytic applications using semantic technologies.Direct POCs /MVPs to explore application of Semaphore, Mark Logic and other semantic technologies for variety of business use cases.Perform emerging technologies evaluation and scanning for new ideas for applying the emerging technologies.Mentor junior ontologists /engineers on information modeling. Participate in the hiring process for new reference data team members.Direct semantic /reference data project teams.Basic Qualifications: Doctorate degree and 2 years of Information Systems experienceORMaster's degree and 4 years of Information Systems experienceORBachelor's degree and 6 years of Information Systems experienceORAssociate's degree and 10 years of Information Systems experienceORHigh school diploma / GED and 12 years of Information Systems experiencePreferred Qualifications: Education/Work ExperienceDegree in Computer Science, Information Science, Information Management, Life Sciences or related field4 years' experience and demonstrated success in taxonomy/ontology development and managementExperience with terminology management platforms (e.g. Smartlogic Semaphore, Top Braid)Experience writing SQL and SPARQL queries.Semantic Technology ExperienceImplementation of Semantic technologies like MarkLogic or Cambridge Semantic.OWL and RDF.Familiarity using Informatica or similar tools for data extraction, transformation and loading.Life Science ExperienceBackground in healthcare and/or clinical sciences and/or life sciences a plusFamiliarity with healthcare taxonomies (UMLS, SNOMED, MedDRA and/or ICD9/10)Experience with Open Semantic Standards like Schema.org and Linked Open Data.Search ExperienceImplementation of search and/or auto-classification systems a plus.Strong communication skills.Join UsIf you're seeking a career where you can truly make a difference in the lives of others, a career where you can work at the absolute forefront of biotechnology with the top minds in the field, you'll find it at Amgen.Amgen, a biotechnology pioneer, discovers, develops and delivers innovative human therapeutics. Our medicines have helped millions of patients in the fight against cancer, kidney disease, rheumatoid arthritis and other serious illnesses.As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other but compete intensely to win. Together, we live the Amgen values as we continue advancing science to serve patients.Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.. Associated topics: data administrator, data analytic, data architect, data quality, data warehouse, data warehousing, erp, hbase, mongo database, teradata

Process Development Scientist - Thousand Oaks

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Position DescriptionAmgen is currently seeking a Process Development Scientist for our Pivotal Drug Product Technologies Group in Thousand Oaks, CA. This group is responsible for late stage drug product formulation and fill/finish process development for various biological modalities (large molecule, RNA, virus). Additionally, the position requires expertise to enhance the way data is analyzed and the use of statistical models to inform decisions throughout drug product development. The Scientist will provide technical and project leadership while integrating information generated by cross functional teams to ensure success through the commercialization process.Responsibilities include: Plan, design, execute, and document laboratory studies related to formulation and fill/finish process development in support of product commercialization and life cycle management Apply basic science/engineering skills and first principle modeling to solve technical problems Participate in Drug Product Commercialization Teams responsible for conducting process development on pipeline products, as well as, supporting commercial products in lifecycle management. Perform data analysis using advanced statistical/analytical techniques with statistical analysis software. Provide support, as needed, to clinical and commercial fill/finish manufacturing operations through process capability analysis, troubleshooting, root cause analysis, and product impact assessments for non-conformance investigations and process changes/improvements. Author and review guideline documents, technical protocols, reports, product impact assessments, and regulatory sections in support of IND and marketing application submissions. Deliver progress reports and presentations to ensure management awareness and engagement of the current status, advancement, and future program functional needs. Ability to travel domestically and internationally up to 10% of the time.Basic Qualifications: Doctorate degree or Doctorate degree completed by March 2019 OR Master's degree & 4 years of scientific experience OR Bachelor's degree & 6 years of scientific experiencePreferred Qualifications: Advanced degree in Chemical Engineering, Biomedical Engineering, Biotechnology, Pharmaceutics or related discipline or Statistics degree with experience in pharmaceutical development and manufacturing 2 years of post-doctoral or industry experience in pharmaceuticals/biotechnology or related field Experience with unit operation (i.e. filling, filtration, mixing, etc.) specific scale down model development, characterization, and scale-up Strong problem solving and effective cross-functional communication skills Experience with coding/scripting for automated data analysis and modeling Experience with data visualization tools or packages, such as Tableau or Spotfire Experience that includes elements of new product development, formulation development, process characterization, equipment design and implementation, technical transfers to global manufacturing sites, statistical process control (SPC), and statistical design and analysis of experiments Proven ability to learn and act on dynamic information at a rapid paceWe understand that to successfully sustain and grow as a global enterprise and deliver for patients - we must ensure a diverse and inclusive work environment.Amgen is committed to unlocking the potential of biology for patients suffering from serious illnesses by discovering, developing, manufacturing and delivering innovative human therapeutics. This approach begins by using tools like advanced human genetics to unravel the complexities of disease and understand the fundamentals of human biology.Amgen focuses on areas of high unmet medical need and leverages its expertise to strive for solutions that improve health outcomes and dramatically improve people's lives. A biotechnology pioneer since 1980, Amgen has grown to be one of the world's leading independent biotechnology companies, has reached millions of patients around the world and is developing a pipeline of medicines with breakaway potential. Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status. Join UsIf you're seeking a career where you can truly make a difference in the lives of others, a career where you can work at the absolute forefront of biotechnology with the top minds in the field, you'll find it at Amgen.Amgen, a biotechnology pioneer, discovers, develops and delivers innovative human therapeutics. Our medicines have helped millions of patients in the fight against cancer, kidney disease, rheumatoid arthritis and other serious illnesses.As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other but compete intensely to win. Together, we live the Amgen values as we continue advancing science to serve patients.Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.. Associated topics: clinical, dietary, disease, health, immuno oncology, kinesiology, pharmacology, physiology, therapy, virus

Pilot Plant - Manager, Downstream - Thousand Oaks

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We are seeking a Manager for the Pilot Plant (based in Thousand Oak, CA) working in the Downstream team.This position will execute a variety of production-related operations in a large scale pilot plant, including but not limited to: performing processing on the floor (purification of Drug Substance); performing supporting activities such as buffer preparation, and equipment set-up/cleaning, execution of downstream operations, and managing staff.Work will also include executing production runs

Associate Manufacturing - Thousand Oaks

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This Cell Culture Manufacturing Associate position will support the re-commissioning and start-up of commercial cell culture drug substance intermediate manufacturing operations in Thousand Oaks, CA. The Sr. Associate will execute production operations on the manufacturing floor including execution and coordination of commissioning and qualification of process equipment. This role will interface between the GMP manufacturing teams in the plant and our partner organizations. Job scope and responsibilities: Execute set up, cleaning, sanitization, analytical testing, and manufacturing operations on the production floor. Ensure all safety and compliance procedures are followed at all times. Participate in the development, execution, and issue resolution associated with process equipment Commissioning, Qualification and Validation. Provide troubleshooting, technical support, and resolution of equipment, automation, and process issues on the manufacturing floor. Write and revise controlled documentation (SOPs, Manufacturing Procedures (MPs), Forms, Technical Reports, etc) Serve as SME for Cell Culture operations including cleanroom Aseptic Technique. Provide training to manufacturing staff on process and equipment. Implement Lean Transformation and OE initiatives, facilitate the drive towards continuous improvement in the plant, and track progress on a plant level. Collaborate with Quality, Engineering, Process Development, Validation, and Operations to resolve manufacturing events in a timely manner. Assure appropriate escalation to various levels of management when personnel and environmental safety, equipment functionality, product supply, or quality are at risk.Collaborate with Quality, Mfg Managers, Plant Engineering, Process Development and Regulatory Compliance staff in cross-functional teams. Apply advanced process, scientific, operational, and compliance knowledge with basic analytical and troubleshooting skills to support manufacturing operations. Participate in the design, development, and implementation of processes in support of the manufacturing floor.Basic Qualifications:Bachelor's degree OR Associates Degree and 4 years of biotech or pharmaceutical manufacturing, process development or quality experience OR High School Diploma / GED and 6 years of biotech or pharmaceutical manufacturing, process development or quality experience Preferred Qualifications:Available for non-standard shifts including nights and weekends. Degree in Chemical Engineering, Industrial Engineering or Life Sciences Technical understanding of drug substance intermediate (Cell Culture) operations Experience with Current Good Manufacturing Practices (cGMP) Ability to be flexible and manage change Experience participating in cross-functional teams Experience in managing multiple, competing priorities in a fast-paced environment Strong scientific, technical interactions with partner organizations such as PD and F&E. Experience in GMP Tech Support roles, GMP operations, process development or scheduling. Experience with execution of Commissioning and Qualification, New Product Introduction, Cleaning Validation, and Process Performance Qualification Experience with aseptic operations in Grade 5 (Class 100) cleanrooms. Technical knowledge of Upstream Drug Substance Intermediate processing and broad understanding of related disciplinary areas - Bioreactors, Roller Bottles, UFDF. Ability to organize, analyze, and interpret technical data through trend analysis, forecasting, modeling, etc. with excellent technical writing ability to convey processing events and conclusions Background in lean manufacturing methodologies and operational excellence Expertise in electronic systems used in manufacturing (MES/Werum, LIMS, Maximo, CCMS, etc.)Amgen focuses on areas of high unmet medical need and leverages its expertise to strive for solutions that improve health outcomes and dramatically improve people's lives. A biotechnology pioneer since 1980, Amgen has grown to be one of the world's leading independent biotechnology companies, has reached millions of patients around the world and is developing a pipeline of medicines with breakaway potential.We understand that to successfully sustain and grow as a global enterprise and deliver for patients - we must ensure a diverse and inclusive work environment. Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status. Join UsIf you're seeking a career where you can truly make a difference in the lives of others, a career where you can work at the absolute forefront of biotechnology with the top minds in the field, you'll find it at Amgen.Amgen, a biotechnology pioneer, discovers, develops and delivers innovative human therapeutics. Our medicines have helped millions of patients in the fight against cancer, kidney disease, rheumatoid arthritis and other serious illnesses.As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other but compete intensely to win. Together, we live the Amgen values as we continue advancing science to serve patients.Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.. Associated topics: bio, biochemistry, biological engineer, biomaterials, biomedical engineer, bioprocessing, enzyme, hereditary, pain, parenteral

Principal Scientist - Global Biosimilars - Thousand Oaks

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Amgen was one of the first companies to recognize the potential of modern biotechnology in developing valuable medicines for patients, and to assemble the diverse set of skills necessary to advance from textbook to applied science. Today, we are applying our deep scientific capabilities from more than three decades of experience to the development of biosimilars and continuing our legacy of providing patients with vital medicines.Advancing science and helping patients - these dual passions are ingrained in our culture. They drive our work, our values, and everything we do at Amgen. For staff around the world, our mission to serve patients and our commitment to science makes Amgen a place where we can make a positive difference in people's lives while pursuing a challenging and fulfilling career.Amgen is looking for an enthusiastic and highly motivated Principal Scientist to join the collaborative and fast-paced Amgen Biosimilars team at the Amgen headquarters campus located in Thousand Oaks, CA. The Biosimilars Analytical Sciences team is responsible for delivering comprehensive similarity testing plans to support the development of Amgen's Biosimilars pipeline. The Principal Scientist is responsible for developing the testing plan to support the assessment of functional similarity across multiple biosimilar programs, as well as successfully managing and executing the plan with internal and external partners. The role uses a breadth of communication expertise, both written and oral, across a broad range of stakeholders, influencing decision-making through negotiation, and delivering results by building productive working relationships across functional areas within the company.The development of a successful biofunctional similarity testing plan includes thorough understanding of the mechanism(s) of action of the molecule, and evaluating the potential impact to clinical efficacy, pharmacokinetics, or safety. A strong grounding in the structure/function relationship of large molecules is also required. Part of the role entails guiding \"fit-for-purpose\" assay qualification to support a rigorous testing plan. The Principal Scientist will manage external interactions and collaborations with partners in academia and at contract research organizations to deliver results within the comprehensive testing plan that fulfill the regulatory requirements for biological assays.The Principal Scientist will support the biosimilar programs through the regulatory approval process in numerous jurisdictions through authoring of regulatory documents, participating in face to face discussions with regulators, and ensuring maintenance of appropriate documents in a compliant manner. Additional responsibilities include supporting the generation of abstracts, posters and publications; participating in national and international scientific meetings.#LI--POSTBasic QualificationsDoctorate degree & 6 years of scientific experience OR Master's degree & 10 years of scientific experience OR Bachelor's degree & 12 years of scientific experiencePreferred Qualifications:PhD in Immunology, Pharmacology, Oncology or Translational Sciences with 7 years experience in the Biotechnology/Pharmaceutical IndustryExcellent interpersonal skills and leadership experience with strong decision making and problem solving skillsExperience critically designing and evaluating biological assays to query diverse biology, particularly in the fields of immunology and/or oncologyExcellent oral and written communication skills supporting internal and external presentations and publicationsDemonstrated track record of independent critical thinking and scientific achievement in research, exemplified by a strong publication record Join UsIf you're seeking a career where you can truly make a difference in the lives of others, a career where you can work at the absolute forefront of biotechnology with the top minds in the field, you'll find it at Amgen.Amgen, a biotechnology pioneer, discovers, develops and delivers innovative human therapeutics. Our medicines have helped millions of patients in the fight against cancer, kidney disease, rheumatoid arthritis and other serious illnesses.As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other but compete intensely to win. Together, we live the Amgen values as we continue advancing science to serve patients.Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.. Associated topics: bacteria, dietician, drug, kinesiology, medical, pharmaceutical, pharmacometrics, protein, therapy, virus

Specialist IS Software Engineer - Thousand Oaks

new1 day ago
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Amgen (NASDAQ:AMGN), a biotechnology pioneer, discovers, develops and delivers innovative human therapeutics. Our medicines have helped millions of patients in the fight against cancer, kidney disease, rheumatoid arthritis and other serious illnesses. With a deep and broad pipeline of potential new medicines, we continue to advance science to serve patients.Amgen is seeking a talented Software Engineer to build leading edge scientific applications with modern technology stacks that will be used by our business partners to drive Amgen's innovation across Operations. The exceptional candidate will join our talented Operations Information Systems (OIS) team to deliver solutions by leveraging best practices in systems development and integrations. This Software Engineer position will report to the Principal Architect, Operations IS. The position can be based at one of Amgen's Research sites: Thousand Oaks - CA, Tampa, FL, or Cambridge - MA campus.The Specialist IS Software Engineer will work as part of an emerging Product Team within the Operations IS (OIS) group to support the Process Development business organization . This team will have a focus on Product Lifecycle Management (PLM) as a strategic platform for digitizing Amgen's product development and commercial advancement.Responsibilities Design, develop, and implement IS solutions to enable end to end digitization of product information and data across Operations.Actively engage with business users to analyze business needs, identify technology solutions gather and document design guided by best practices in Agile solution development.Perform hands-on development of technology solutions including configuration of commercial software as well as extensions and integrations through coding/custom developmentServe as lead Solution Engineer: Lead in-house solution development as well as oversee supporting team of external contractors and consultantsCollaborate with IS Architects and System Owners to implement an integrated solution across PLM, ERP, MES, Enterprise Data Lake, and lab execution systemsReview project deliverables throughout development to ensure quality and traceability to requirements and adherence to all quality management plans and standards. Participate in IS quality validation reviews.Oversee the backlog of requirements/user storiesSupport day-to-day sustainment and production run support activitiesBasic Qualifications:Doctorate DegreeORMaster's Degree AND 3 years of Information Systems experienceORBachelor's Degree AND 5 years of Information Systems experienceORAssociate's degree AND 10 years of Information Systems experienceORHigh school diploma/GED AND 12 years of Information Systems experiencePreferred Qualifications:Experience designing, configuring and coding software including custom development and commercial software packages using APIsExperience with integration standards, including Web Services, SOAP, REST, as well as middleware platforms, preferably MulesoftSolid understanding of PLM architecture and configuration, including: interfaces, item libraries, engineering change orders (ECOs), Bills of Materials (BOM) management, and lifecycle states.Familiarity with Product Lifecycle Management practices in the biotech and pharmaceutical industries is preferable; experience with the composition and assembly of filing submissions within the Bio-Pharma lifecycle a plusSolid depth or breadth of expertise with offerings within the PLM solution landscape - including Oracle AgileExperience working with Big Data integration and Analytics a plusExperience integrating solutions with ERP, and MES platforms as plusGood overall understanding of business, manufacturing, and laboratory systems common in the pharmaceutical industry, as well as the integration of these systems through applicable standards.Understanding of FDA regulations governing computer system validation and operation in biotech manufacturing and laboratory areas.Excellent verbal, written, and interpersonal communication skills, including the ability to set the context and present on complex subjects to senior management in a clear and concise manner.Experience building productive working relationships with business clientsStrong leadership, project management skills.Amgen focuses on areas of high unmet medical need and leverages its expertise to strive for solutions that improve health outcomes and dramatically improve people's lives. A biotechnology pioneer since 1980, Amgen has grown to be one of the world's leading independent biotechnology companies, has reached millions of patients around the world and is developing a pipeline of medicines with breakaway potential. Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status. Join UsIf you're seeking a career where you can truly make a difference in the lives of others, a career where you can work at the absolute forefront of biotechnology with the top minds in the field, you'll find it at Amgen.Amgen, a biotechnology pioneer, discovers, develops and delivers innovative human therapeutics. Our medicines have helped millions of patients in the fight against cancer, kidney disease, rheumatoid arthritis and other serious illnesses.As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other but compete intensely to win. Together, we live the Amgen values as we continue advancing science to serve patients.Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.. Associated topics: application, backend, c c , c , devops, perl, sdet, software developer, software development engineer, software programmer

Director, Modeling and SImulation - Thousand Oaks

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Amgen is a values based organization with a powerful sense of shared purpose toward our mission: to serve patients. We encourage our team members to have fulfilling and meaningful careers through challenging assignments, career development, and valuable opportunities such as this.Biotechnology opened the door to new types of medicines based on nature's own building blocks. No company has done more to advance this revolution than Amgen & the company's broad toolkit of drug modalities just got larger www.amgenscience.com/the-shape-of-drugs-to-come . The Clinical Pharmacology, Modeling & Simulation Department at Amgen (Thousand Oaks, CA) is seeking a Director, Modeling and Simulation.Responsibilities:The Director will be responsible for the development and implementation of the modeling and simulation strategies and execution of tasks for clinical development candidates across multiple novel modalities including T-cell engagers and cellular therapies in addition to monoclonal antibodies and small molecules. Key responsibilities include leading a team of modelers responsible across multiple indications in the oncology therapeutic area for:Conducting PK/PD and exposure-response analyses of data from early to late phase clinical studies using pharmacostatistical and relevant state of the art modeling and simulation techniquesPerforming meta-analysis using proprietary and/or literature dataParticipating in cross-functional project teams and providing scientific input for dose selection for early and late stage clinical study designs using quantitative methodsContributing to clinical pharmacology plans by establishing and implementing high impact modeling and simulation strategy for clinical development candidatesAuthoring PK/PD reports and contributing to summary documents for regulatory submissions.Basic Qualifications:Doctorate degree and 4 years of Modeling & Simulation scientist in the Biotechnology/ Pharmaceutical IndustryORMaster's degree and 7 years of Modeling & Simulation scientist in the Biotechnology/ Pharmaceutical IndustryORBachelor's degree and 9 years of Modeling & Simulation scientist in the Biotechnology/ Pharmaceutical IndustryPreferred Qualifications:PhD in applied (bio)statistics, (bio)engineering, applied biomathematics/biophysics or related fields with equivalent professional degrees10 years of experience as Modeling & Simulation scientist in the Biotechnology/ Pharmaceutical Industry.Experience mentoring and supervising junior modelersDeep understanding of clinical pharmacology and early and late phase clinical developmentExpertise and past hands-on experience analyzing pharmacokinetic, efficacy and safety data from clinical trials using advanced pharmacometric or statistical modeling methodologies and conducting clinical trial simulations to assist study designExpertise in standard pharmacometric software (e.g. NONMEM, R, SAS, MATLAB) and programming languagesExpertise in binary and categorical data analyses, time-to-event (hazard) models, Poisson models, logistic regression, MCMC and Bayesian methods as applied to exposure-response analyses, meta-analyses and Population PK and PKPD analysisExpert knowledge in developing modeling analysis plans, population PKDPD and translational modeling strategies, developing clinical study designs and dose optimizationTrack record of regulatory filings (NDA/BLA) and responding to regulatory agency questions and knowledge of global regulatory requirements and guidances on quantitative analysesExperience guiding the development/maintenance pharmacometric infrastructure, justifying and implementing innovative pharmacometric software/tools, leading innovative methodology/algorithm development for modeling and simulations, and organizing trainings and educations to embrace cutting-edge technologies in pharmacometricsExperience recognizing and anticipating discovery/translation/development problems that can be addressed by applying quantitative methods and finding effective solutions in partnership and collaboration with cross-functional teams to enable decision-making. Track record of influencing a broad spectrum of stakeholders toward achieving business goalsExcellent interpersonal, verbal and written communication skills and the ability to function in a highly matrixed team environment are essential.Previous record of scientific contributions through peer-reviewed articles and external presentationsOur culture is what makes Amgen a special place to work. We have a powerful shared purpose around our mission - to serve patients. We respect one another, recognize contributions, and have embedded collaboration, trust, empowerment and inclusion in all that we do.Amgen is committed to unlocking the potential of biology for patients suffering from serious illnesses by discovering, developing, manufacturing and delivering innovative human therapeutics. This approach begins by using tools like advanced human genetics to unravel the complexities of disease and understand the fundamentals of human biology.Amgen focuses on areas of high unmet medical need and leverages its expertise to strive for solutions that improve health outcomes and dramatically improve people's lives. A biotechnology pioneer since 1980, Amgen has grown to be one of the world's leading independent biotechnology companies, has reached millions of patients around the world and is developing a pipeline of medicines with breakaway potential.#LI-POSTJoin UsIf you're seeking a career where you can truly make a difference in the lives of others, a career where you can work at the absolute forefront of biotechnology with the top minds in the field, you'll find it at Amgen.Amgen, a biotechnology pioneer, discovers, develops and delivers innovative human therapeutics. Our medicines have helped millions of patients in the fight against cancer, kidney disease, rheumatoid arthritis and other serious illnesses.As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other but compete intensely to win. Together, we live the Amgen values as we continue advancing science to serve patients.Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.. Associated topics: bio, biology, biomaterials, biomechanics, bioprocess, biosynthetic, fermentation, hereditary, metabolic, pain

Associate Project Mgmt Coordinator - CA - Thousand Oaks

new1 day ago
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Support project management activities. Coordinate technical requirements of meetings including projector, laptop, and teleconference requirements. Take and/or type meeting minutes. Aids in various administrative tasks regarding project budgets and schedules, such as monitoring purchase orders and project spend, and posting items to project folders. Keep information up to date including schedules, budgets, and the project information in e-Builder or other appropriate application. Should be organized, reliable, and respond promptly to requests. Perform tasks independently with minimal supervision, in addition to working on teams to accomplish tasks. Coordination with the project team and project manager is essential. Skills: Construction or real estate support experience; MS Office proficiency; SAP & e-Builder experience preferred; strong written and verbal skills Basic Educational Requirement: High-school diploma or GED

Business System Analyst - Thousand Oaks

new1 day ago
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Amgen (NASDAQ:AMGN), a biotechnology pioneer, discovers, develops and delivers innovative human therapeutics. Our medicines have helped millions of patients in the fight against cancer, kidney disease, rheumatoid arthritis and other serious illnesses. With a deep and broad pipeline of potential new medicines, we continue to advance science to serve patients.Amgen is seeking an Information Systems, Specialist IS Business System Analyst located at its headquarters in Thousand Oaks, CA reporting to the Sr. Manager of Clinical Data Analysis IS services and primarily responsible for leading IS Services for three business capabilities: Statistical Study Design, Clinical Data Standards, and Clinical Data Statistical Analysis, and a shared SAS Analytical Platform Service. Collaborate with business partners and other IS service leads to define roadmap in support of business strategy and goals.Primary responsibilities may include: Leadership in defining technical and process improvements with many groups of business, IS and vendors to plan and implement City planning for future (ecosystem rationalization, cloud adoption, license negotiation, Cloud adoption, etc.) Leadership in driving innovative solution for Innovative Study Design by using new data science and machine learning Leadership to deliver innovative solution using R, Python, AWS, Databricks, and other latest technologies for Clinical Study Design Product ownership of enterprise class SAS Grid ecosystem used by thousands of users with global print spanning multiple department and external partners Accountable along with Amgen Service Providers to ensure 24x7 availability of mission critical applications Accountable to deliver IS service in alignment with business and IS strategy Interact with business clients, IS management and suppliers to lay out a technology roadmap, build business cases, manage projects to achieve the roadmap, and provide vendor oversight to manage system production activities Responsible for a variety of systems that support the business capabilities Partner with business and technology teams to elicit, analyze, translate, and document business requirements into technical requirements and solutions Responsible for managing key client relationships that are essential for the capability that this role will support Work directly with business partners to analyze current processes and capabilities to identify opportunities for improvements Manage vendor, service costs, requirements elicitation and documentation, market/vendor analysis, identification and management of risks Work closely with architects and technical SMEs, and enabling user adoptionBasic Qualifications:Doctorate degreeOR Master's degree and 2 years of Information Systems or Statistical Analysis experienceOR Bachelor's degree and 4 years of Information Systems or Statistical Analysis experienceOR Associate's degree AND 10 years of Information Systems or Statistical Analysis experienceORHigh school diploma/GED AND 12 years of Information Systems or Statistical Analysis experiencePreferred Qualifications: Good understanding of Artificial intelligence and data science Good understanding of full stack development and DevOps Experience developing multiyear technology plan Understand business functionality and translate it into application requirements Ability to create compelling business cases with accurate cost and effort estimations Excellent understanding of business complexity and project interdependencies Intellectual curiosity and the ability to question thought partners across functional areas Outstanding written and verbal communication skills Ability to explain complex technical concepts to non-technical clients Analytical skills and techniques to evaluate interpret and resolve complex situations/problems using multiple sources of information Knowledge of SAS GRID architecture, Real world data, Clinical trial data, and analytics and visualization solutions Familiar with SAS, R, Python programming Familiar with AWS architecture and Databricks Understanding of SDLC (System Development Life Cycle) methodologies Experience in biotechnology or other healthcare environment Sharp learning agility, problem solving and analytical thinking Ability to lead and influence clients, other business analysts, and technical team members Experience delivering solutions in a managed service delivery model Experience managing regulated systemsAmgen is committed to unlocking the potential of biology for patients suffering from serious illnesses by discovering, developing, manufacturing and delivering innovative human therapeutics. This approach begins by using tools like advanced human genetics to unravel the complexities of disease and understand the fundamentals of human biology.Amgen focuses on areas of high unmet medical need and leverages its expertise to strive for solutions that improve health outcomes and dramatically improve people's lives. A biotechnology pioneer since 1980, Amgen has grown to be one of the world's leading independent biotechnology companies, has reached millions of patients around the world and is developing a pipeline of medicines with breakaway potential.Join UsIf you're seeking a career where you can truly make a difference in the lives of others, a career where you can work at the absolute forefront of biotechnology with the top minds in the field, you'll find it at Amgen.Amgen, a biotechnology pioneer, discovers, develops and delivers innovative human therapeutics. Our medicines have helped millions of patients in the fight against cancer, kidney disease, rheumatoid arthritis and other serious illnesses.As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other but compete intensely to win. Together, we live the Amgen values as we continue advancing science to serve patients.Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.. Associated topics: business, business intelligence, business systems analyst, examiner, financial reporting analyst, government, guidance, investment analyst, law, refine

CNA - Certified Nursing Assistant - Thousand Oaks

new1 day ago
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Comfort Keepers Home Care, a World Leader, is hiring caregivers, homemakers, companions, CNAs and LVNs with a big heart and strong work ethic to provide non-medical care that helps seniors remain in their own homes and maintain full, independent lives. Our Comfort Keepers elevate the human spirit!Would you like to make a real difference in the life of a senior, working for a World Leader? Apply to be a Comfort Keeper!Comfort Keepers was voted as one of the TOP FOUR Employers in this area (Regional News site, 2018)!DUTIES We are looking for compassionate individuals to provide a range of services; including preparing basic meals, providing light housekeeping, laundry assistance, driving, dressing, grooming, fall prevention and companionship to our wonderful seniors. Some of our caregivers also provide mobility and personal hygiene assistance, but it is not a requirement of the job. REQUIREMENTS:You need to have caregiving experience, either paid or volunteer (like taking care of a loved one)OR Be a CNA or LVN (an expired license is okay!)You also need to have a dependable car that is your own to drive, a valid California Driver's License, valid car insurance, and be legally able to work in the United States.Our Comfort Keepers will also be LiveScan fingerprinted through the DOJ.Please live in the Ventura County, Conejo Valley, or West Valley areas Comfort Keepers is a World Leader, part of an international network of 700 officesComfort Keepers is the Ventura County Star READER'S CHOICE AWARD WINNER in 2014, 2015, 2016, 2017, and 2018 for Senior Services! BENEFITS TO YOU:* WE ARE EXTREMELY BUSY!* $100 Sign-On Bonus for current CNAs(easy conditions apply)* Healthcare Insurance for those who qualify- Medical, Dental, Vision * Flexible hours- Part-time, Full-time, Days, Afternoons, Nights, Overnights, and/or Weekends* Free In-Person Career Development Classes from our Comfort Keepers Learning Academy!* Mileage reimbursement* Amazing support team!* Monthly Caregiver Appreciation Days!* Excellent mentoring* Caregiver Learning Workshops - our Caregivers and CNA's love them!* Hundreds of free online career development / training classes* Paid sick leave* Higher pay rate for weekends, depending on your base rate* 10 Types of Bonuses* YOU CHOOSE WHICH CITIES YOU WOULD LIKE TO WORKWe service Camarillo, Ventura, Oxnard, Simi Valley, Moorpark, Newbury Park, Thousand Oaks, Westlake Village, Agoura Hills, West Hills, Calabasas, and surrounding citiesHOW DO I APPLY?BEST WAY is to apply online at:ckthousandoaks.clearcareonline.com/apply/OR come by our office to complete your online application8:45 AM to 4:00PM, Monday through Friday at3249 Old Conejo Rd.Newbury Park, CA 91320(805) ###-####Please be sure to check your voicemails and emails pretty often, so we can more easily connect with you. Thank you! We are also looking for caregivers!Great careers await you at Comfort Keepers! Associated topics: anesthetist crna, board, cns, family, gyn, neighborcare, nurse practitioner, ob, prn, specialis

Undergrad Co-op - OPS (Pilot Plant) - Thousand Oaks , CA

new2 days ago
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…advancing science to dramatically improve people's lives. We are seeking a co-op for the Thousand Oaks , CA Pilot Plant to execute a variety of

jobs byJuju.com

Experienced CDL-A Truck Drivers ( Thousand Oaks , CA )

new2 days ago
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…Join Swift s Driving Force. Swift values the years of experience under your belt and wants you to join the most powerful fleet on the road. To be a powerful force,

jobs byJuju.com

Physical Therapist (PT) Thousand Oaks CA 91361

7 days ago
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Seeking a full time and part time Physical Therapist (PT) for an outpatient private practice in Thousand Oaks CA 91361 State of the art facility and no hospital work or call schedule. We emphasize ...

jobs byZipRecruiter

Speech Language Pathologist opening in Thousand Oaks, CA area

7 days ago
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We are currently interviewing for a job as a Speech Language Pathologist to work with our students in the Thousand Oaks, CA area. We need a dedicated SLP to address some of the background work with ...

jobs byZipRecruiter

Clean-Room Assemblers Thousand Oaks Ca.

13 days ago
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Now HIRING 2nd Shift Clean-Room Assemblers Job Description Growing manufacturing company in Thousand Oaks is looking for assemblers with clean room experience for their second shift. Great ...

jobs byZipRecruiter

Full TIme School Based LVN Job Available near Thousand Oaks, CA

14 days ago
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We are looking to set up interviews for experienced LVN's ready to work full time in a school setting near Thousand Oaks, CA . br> br> Job Duties and Requirements: br> br> br> * Trach/Vent Experience ...

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Registered Nurse Case Manager - Thousand Oaks

23 days ago
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…are available, ie, Thursday-Monday Locations: Ventura County covers the following cities: Thousand Oaks , Agoura Hills, Moorpark, Newbury Park, Oak Park, Simi

jobs byJuju.com

Automotive Inventory Photographer - Thousand Oaks, CA

about 1 month ago
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Automotive Inventory Photographer - Thousand Oaks, Simi Valley, Oxnard - Req. #1165 Keywords: Task oriented Goal oriented Thrives on independence Responsive with a sense of urgency Xcite Advertising ...

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Physician / Family Practice / California / Permanent / Urgent Care / Thousand Oaks, CA Job

about 2 months ago
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Physician / Urgent Care / Thousand Oaks, CA Urgent Care Physician Needed. We are one of the area's leading providers of quality, caring, and convenient urgent care. We are a physician-driven company ...

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Sales Specialist- Rheumatology- Thousand Oaks CA - Remote

2 months ago
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Novartis is recruiting for a Rheumatology Sales Specialist role. This position will be located in Thousand Oaks , CA . The position goes from Thousand

jobs byJuju.com

Thousand Oaks, CA: School Speech-Language Pathologist

8 months ago
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Soliant has partnered with a client near Thousand Oaks, CA to interview Speech-Language Pathologists for the upcoming school year. Details of the position below: * 2018-2019 * Full-time * Caseload ...

jobs byZipRecruiter

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