Location: Menlo Park, US Reporting to: VP, Vector Operations The Manager, Vector Production will assist in the oversight activities related to the development and cGMP production of lentiviral vectors at contract manufacturing organizations (CMOs). Such activities will include the scale-up, validation and execution of manufacturing processes and controls to support Orchard Therapeutics innovative cell and gene therapy product programs from Phase I clinical trials through to commercial. Responsibilities Assist with the transfer of plasmid and lentiviral vector production processes and controls from academic collaborators to company designated CMO's Help to coordinate and manage the GMP production, testing and fill finish of lentiviral vectors at CMO's Provide on-site person-in-plant oversight during production campaigns and key development/validation activities Assist with the reporting, investigation and resolution of deviations encountered during GMP production activities Provide expert compilation, review, editing and approval of master production records, standard operating procedures, development/validation protocols and reports Provide expert review and approval of executed batch, records, test records and associated documentation for release of lentiviral vector lots and for plasmid lots used in their production Help to co-ordinate production activities with the research, pre-clinical development, QA, QC, clinical development, commercial and project management departments to ensure the successful achievement of company timelines and milestones Ensure the ongoing security of the supply chain for raw materials and intermediates to assure the uninterrupted performance of lentiviral production operations and provision of material for pre-clinical, clinical and commercial programs Other activities as may be assigned Requirements Job Requirements The ideal candidate for this position will have in-depth experience of the large-scale cGMP production of viral vectors, especially lentiviral vectors, including upstream cell culture, downstream processing, and fill finish operations. Candidate must possess: BS or MS in bioprocessing, chemical engineering, vector biology, or biological sciences Ability to work independently or with minimal oversight Strong experience in the biotechnology or pharma industry with a primary focus on upstream cell culture, transfection, downstream processing, and fill finish operations for viral vectors and/or biologics Proven track record of working in development, validation and production operations Experience with: Mammalian cell and microbial cell culture systems Different bioreactor production systems and scales, including disposable single-use bioreactor systems Validation of manufacturing processes and controls Knowledge of FDA, EMA, GMP and ICH regulatory requirements Knowledge of Quality Systems and QBD as they relate to GMP production operations, process optimization and process validation Other Requirements This position requires on site person-in-plant presence at CMO's and contract vendors on a potential global basis. Therefore, ability to travel is a pre-requisite Personnel and project management skills Organizational skills Excellent written and oral communication skills Ability to operate in a fast-paced, multi-disciplinary industrial environment Experience of facility, and production equipment design and validation, including IQ, OQ & PQ preferred Benefits The successful candidate will enjoy a competitive base salary and the opportunity to participate in incentive compensation programs, including a stock option plans. Orchard Therapeutics, Ltd. offers a comprehensive benefits program, including: medical, dental and vision care; paid vacation and holiday time; access to a voluntary 401(k). Orchard Therapeutics is an equal opportunity employer. Notice to All Applicants: Orchard Therapeutics participates in E-Verify For further information on this role do not hesitate to email [email protected] RECRUITERS All employment offers and CV's are managed through our Human Resources Department and all candidates are presented through this avenue. Therefore, the Human Resources Department at Orchard Therapeutics requests that recruiters are not to contact Orchard Therapeutics employees directly to present candidates. Complying with this request will be a factor in determining future professional relationships with Orchard Therapeutics. Orchard Therapeutics will not accept unsolicited resumes from any source other than directly from candidates for either current or future positions. Submission of unsolicited resumes in advance of an agreement between the Human Resources Department and the recruiter does not create any implied obligation on the part of Orchard Therapeutics.
Behavioral Science and Interventions Team : Across JUUL we are extremely mission-driven and carefully consider how user and product characteristics, physiology, and customer experience can improve ...jobs by
Development and optimizations of state-of-the-art deep learning models using Deep Learning frameworks, covering computer vision, object detection and localization, speech recognition, natural language processing, reinforcement learning etc. Work with framework software developers to facilitate end-to-end optimization Distribute the model training and inference into multi-node systems, allowing scalable optimization and performance. Design and enable next generation deep learning systems. Development of deep learning algorithms to exploit novel distributed processor architectures. The ideal candidate should exhibit the following behavioral traits: - Problem-solving skills - Ability to multitask - Strong written and verbal communication skills - Ability to work in a dynamic and team-oriented environment Qualifications You must possess the below minimum qualifications to be initially considered for this position. Preferred qualifications are in addition to the minimum requirements and are considered a plus factor in identifying top candidates. Experience listed below would be obtained through a combination of your school work/research and/or relevant previous job and/or internship experiences. Master’s or PhD in Computer Science, Electrical Engineering or any related fields (Statistics, Applied Math, or Computational Neuroscience) 1 years of experience in the following area: • Background in DL, ML algorithms and model development. • Experience designing and developing professional software using Python, C++. Preferred Qualifications: • Experience with model tuning and optimization through data science projects or data competitions • Familiarity with DL, ML frameworks (eg. TensorFlow, Caffe, Neon, PyTorch etc.) • Familiarity with details of implementing algorithms on multi-core CPUs, clusters (MPI), GPUs, heterogenous clusters, distributed frameworks (eg. GraphLab, Spark, Hadoop)
Behavioral Science and Interventions Team : Across JUUL we are extremely mission-driven and carefully consider how user and product characteristics, physiology, and customer experience can improve ...jobs by
We seek postdoctoral appointees to develop solutions to important national security problems, particularly in the arena of coupling algae biomass production with environmental remediation. Our objective is to optimize attached algae systems for variety of potential source waters guided by an underlying understanding of the key phenomena, to create game-changing solutions. In particular, we are developing advanced substrates and fluidic designs for coupling cultivation of native periphyton with introduced algae species to provide high productivity designer consortia. On any given day, you may be called on to: Be responsible for development and implementation of scalable means of attached algae cultivation, including harvesting and characterization; Be part of an interdisciplinary team that includes biochemists, and chemical and bioprocess engineers at both the staff and postdoctoral level, conducting fundamental and applied research using both experimental and computational tools. Qualifications We Require PhD in Chemical, Biosystems, or Bioprocess Engineering or related field with a strong algae emphasis during the thesis work, and demonstrated ability to identify and implement material solutions at the intersections of fields such as materials science and biology; Significant experience in R&D related to water treatment, geographic information systems for resource assessment, or hydrodynamic phenomena; A record of publications in peer-reviewed journals and presentations at scientific conferences. Qualifications We Desire Expertise in any of the following areas is desirable: Computational fluid dynamics; Systems integration; Llife-cycle assessment; Technoeconomic analysis. Position Information This postdoctoral position is a temporary position for up to one year, which may be renewed at Sandias discretion up to five additional years. The PhD must have been conferred within five years prior to employment. Individuals in postdoctoral positions may bid on regular Sandia positions as internal candidates, and in some cases may be converted to regular career positions during their term if warranted by ongoing operational needs, continuing availability of funds, and satisfactory job performance. About Our Team The Biomass Science and Conversion Technology department is dedicated to developing and advancing innovative technologies for producing the next generation of biofuels. Our multidisciplinary staff represents a diverse range of backgrounds and skill sets: molecular biology, chemistry, chemical and biochemical engineering, biophysics, computational science, and biochemistry. We partner broadly with other Sandia departments as well as other national laboratories, industry, and universities to develop practical, science-based solutions to national energy goals. We also play an essential role in the DOE Joint BioEnergy Institute (JBEI), one of three Bioenergy Research Centers in the Nation advancing the next generation of biofuel technologies.
We are a nationwide staffing firm, currently seeking a Research Associate (BioAnalytical Sciences) for a prominent client of ours in South San Francisco, CA . Here is a brief job description: · ...jobs by
Financial Planning & Analysis is responsible for being objective and strategic financial partners, leading collaborative cross-functional effort to drive relevant, flexible and efficient financial planning and analysis that supports our key business decisions. Analyzes business trends leads and aligns financial forecasts and long range planning processes with our business leaders. Drives business value by providing financial and analytical counsel to facilitate decision-marking around strategic business initiatives. Prepares monthly financial reporting including variance and financial statement analysis. Able to clearly communicate a cohesive and concise story around business drivers behind financial data and potential implications on future results. Creates financial models and scenarios as a key input for business planning decisions in areas such as capital deployment, sourcing, product development, marketing strategies, and acquisitions. Manages annual budget processes, incorporating business initiatives, economic trends and operational effectiveness. Aligns budget to business strategies and gains alignment from business partners. Performs customer and product profitability analysis and makes investment and pricing decisions. Identifies opportunities to drive revenue growth, margin expansion and a more favorable mix (i.e., driving preferred products and services). Understands market dynamics and competitors. Conducts complex analysis, synthesizes and summarizes implications to business, influencing business partners using analytics and business understanding. Identifies and executes upon process improvement opportunities. Demonstrates proficiency of technical tools and financial systems. Serves as an objective financial steward with an enterprise perspective, safeguarding our companys assets. Ensures strong controls are in place and the companys intellectual property is protected. Accountabilities Serves as Business Partner to the International Commercial FP&A teams spanning 5 regions Coordinates monthly reporting and forecast deliverables for International teams Drives month-end processes to ensure accurate management reporting Responsible for monthly Medical Segment FX impact calculation and reporting in partnership with Treasury Partners with Tax to develop quarterly Legal Entity forecast for the Medical Segment Qualifications Bachelors degree in business related field, or equivalent work experience 4 years experience in related field What is expected of you and others at this level Applies comprehensive knowledge and a thorough understanding of concepts, principles, and technical capabilities to perform varied tasks and projects May contribute to the development of policies and procedures Works on complex projects of large scope Develops technical solutions to a wide range of difficult problems. Solutions are innovative and consistent with organization objectives Completes work independently receives general guidance on new projects Work reviewed for purpose of meeting objectives May act as a mentor to less experienced colleagues
A Research Technician job in San Diego, CA is available through Adecco Medical and Science. The Research Technician is responsible for working in high-impact projects with implications in cancer ...jobs by
Job Description: We are seeking a skilled molecular biologist/immunologist/biochemist at the Scientist level to work on a variety of cutting edge project in immune-oncology field. The candidate will be expected to help progressing our pipeline by generating cell-lines, developing assays, protein/peptide antigens, and helping in mechanistic understanding of various IO targets. Responsibilities • Apply molecular and cell biology techniques to design and generate transient and stable cell-lines using various techniques including lentiviral transduction and CRISPR • Utilize expertise in biochemistry to design and generate functional cell-based assays to support biology, antibody generation, and mechanistic studies • Working knowledge of protein chemistry to assist in design and generation of protein/peptide antigens. • Identify and implement methodologies to enhance cell-line, antigen, and assay functionalities. • Working at the interface between protein engineering and biology • Immunology background is a plus • Accomplish goals under project team time lines. Qualifications • Ph.D. and postdoctoral work in Molecular & Cell Biology, Immunology, Biochemistry or similar field with 2 years post Ph.D. experience • Experience in cell-line generation for immunizations and functional assays. • CRISPR and lentivirus experience highly desirable • Experience in generation of protein antigens is highly desired but not required. • Demonstrated ability to work in a multidisciplinary biologics discovery team • Excellent written, oral, and organizational skills
You will be assisting scientists in the operation of our services and the manufacturing of our products so that everything runs smoothly and customers get what they need. A desire to learn about ...jobs by
The Outcomes Research Scientist (ORS) is responsible for developing patient-centered and fit-for-purpose measurement strategies, and the execution of pre-approval and post-approval drug development programs across Roche. The ORS may work across multiple pipeline and marketed medicines and collaborate with clinical development teams, lifecycle teams, access teams and functional teams to generate data and strategies that demonstrate the benefit of Roche products. The ORS provides input on various deliverables including, but not limited to: study protocols, statistical analysis plans, clinical study reports and target product profiles. They may also work with regulatory colleagues to provide input on endpoint-related strategies for EMA and FDA, and Global Access colleagues to increase patient access to approved therapies. The ORS will be involved in a wide range of activities including developing conceptual models, hierarchical endpoint models, conducting endpoint reviews, scientific communications and, where required, developing, modifying and validating clinical outcome assessments (COAs). The ORS may have some responsibility for vendor management, including scope of work development, contract initiation, monitoring project delivery and managing budgets. They may also influence the external environment by contributing to pre-competitive consortia such as C-Path, ISOQOL, etc. Key Responsibilities & Accountabilities Clinical Development & Patient Access: Generates and evaluates patient-relevant evidence to support external and internal decision making (e.g., Target Product Profiles, Clinical Development Plans,etc.). They provide input and sit on teams focused on development, study execution, and access and commercialization. Study Planning: Provides recommendations on endpoints and strategies for evidence generation. Reviews study protocols, inputs on COA-related sections of statistical analysis plans. Analysis and Reporting: Inputs/reviews clinical study reports and target product profiles. Inputs and/or leads dissemination of PCOR-related content and activities e.g. manuscripts, conference abstracts/presentations Functional Area: Understands and applies business requirements and processes. Participates in functional training. Keeps abreast of new developments in patient-centered outcomes research, drug development, and regulatory guidance. Participates in PCOR and cross-functional initiatives. Participates in the development of functional processes. Recognized expertise in COA selection, development, validation and demonstration of clinically meaningful change. Builds and maintains collaborative relationships and partnerships with key TA/Franchise colleagues to effectively consider strategic approaches to drug development, clinical trials, and to meet operational requirements of development plans within the TA/Franchise (this includes but is not limited to PD functions, as well as Commercial, Market Access, and key country affiliates (US/Genentech, UK and Germany). Contributes to development, review, interpretation of guidances and other similar documents when issued by external bodies (e.g. FDA, EMA, Other Global Regulatory bodies, Health Technology Assessment bodies, etc.). Active participation in key external initiatives that increase the success of our molecule programs (e.g. C-Path, Duke Margolis, ISOQOL, ISPOR, Friends of Cancer Research). Delivers on the PCOR vision to generate patient-relevant information through collaboration across the organization spanning early development through post-approval phases. People Development and Management: Mentors and supports other scientists on request. Required Qualifications and Knowledge MPH, MSc, PharmD or PhD in Outcomes Research, Public Health, Psychometrics, Psychology or similar areas of academic discipline, or significant expertise in target area. Pharmaceutical industry experience preferable. Strong knowledge of English in a business environment. Experience conducting qualitative or quantitative research, survey research, and endpoint development. Required Experiences and Competencies Understands and applies business requirements and processes. Accomplishes responsibilities with little supervision. Effective communication and collaboration skills. Ability to influence others without authority. Good project management skills (including ability to manage scope and effectively delegate to other functions, staff, contractors and external vendors). Strategic agility (including problem-solving and critical thinking skills, ability to drive novel measurement strategies, agility that extends beyond PCOR elements of drug development), adaptability. Demonstrated interest and ability to learn new things; takes initiative, welcomes problems as challenges, finds solutions to technical problems, interpersonal challenges, and drives change when required. Ability to build and foster strong collaborative networks of internal and external partners across sites, functional areas, and business units, and outside Roche. Ability to champion processes and practices to ensure functional norms and best practices are being uniformly applied. Understanding and respect of cultural differences when interacting with colleagues in the global work place. Effective mentoring of other scientists.
Opportunity to work for a company that creates cutting edge scientific solutions * Cross functionality (Customer Support, Customer Service, Research and Development, Product Management, etc.) * Great ...jobs by
Adroit Resources: Working with great, fast growing companies and the best talent Location: San Francisco, CA Contract Long-Term Job Description: Scale new algorithms to large data sets. Train algorithms to apply models to new data sets. Utilize system tools including (MySQL, Hadoop, Weka, R, Matlab,ILog). Validate models and algorithmic techniques. Work with cross-functional partners across the business - provided by Dice data, python, hadoop
Lab Manager/Lead Scientist position available in the Division of Hematology/Oncology at the University of California San Francisco. Our laboratory is pursuing novel immunotherapeutic approaches for ...jobs by
Description Fate Therapeutics is seeking an enthusiastic and skilled cell biologist to join our company’s Process Sciences and Assay Development team to support the company’s off-the-shelf cellular immunotherapy programs. The successful candidate will join a multidisciplinary team pursuing the derivation of hematopoietic cells, particularly engineered hematopoietic progenitor stem cells (eHPSCs), from iPSCs for cellular therapeutic purposes. The candidate will work with project teams to develop robust culture, differentiation, purification and characterization methods for human induced pluripotent stem cells (iPSC) derived cell therapy products. Candidates must have extensive cell culture experience, in particular with embryonic stem cells (ESCs) or iPSCs, and an understanding of immunology is preferred. This position is located at our corporate headquarters in San Diego, CA and reports to the Development Scientist, Cell Therapy. Responsibilities • Maintenance and expansion of iPSC lines • Perform, optimize, and analyze experiments involving the in vitro differentiation, expansion, and production of iPSCs towards eHPSCs • Produce iPSC-derived hematopoietic cells to support the development of off-the-shelf cellular therapies • Phenotypic and functional characterization utilizing flow cytometry, FACS sorting, gene expression, NK cell / myeloid / T cell differentiation assays • Design and execute on experimental plans to achieve project goals within a given time constraint • Implement procedures to standardize Fate’s hematopoietic differentiation platform • Data analysis, data interpretation, detailed record keeping, and SOP writing • Presentation of data to Tech Ops group and larger program-specific teams • Work closely with Fate’s manufacturing, QC, research and development teams to solve technical challenges • Ordering and maintaining stocks of lab reagents Qualifications • B.S. minimum 8 years of relevant experience or M.S. minimum 6 years of relevant experience in stem cell biology, developmental biology, biomedical engineering, immunology or other related fields • Expertise in mammalian cell culture • Prior hands-on experience with iPS/ES cell culture and differentiation is preferred • Hands-on laboratory experience outside of the classroom in an industry setting is desirable • Prior experience with multi-color flow cytometry data acquisition and analysis • Applicants should possess a strong work ethic, initiative, the ability to multi-task, and a desire to acquire new technical skills • Excellent communication, time management, record keeping, and data analysis skills • Background in immunology is a plus Working Conditions and Physical Requirements • Will require working with cells and cell lines of human and/or animal origin • Will require working with hazardous materials • 100% on-site work at corporate headquarters in San Diego, CA • Evening and weekend work as necessary
Under the general supervision of the Public Service Administrator/Department Director, the Clinical Laboratory Scientist/Technician performs both general and specialized techniques in molecular ...jobs by
Minimum Required Skills: Python, Automated Testing, Powershell / Shell, Networking (TCP/IP), AWS, Virtualization, Selenium, Django / Flask, Linux If you are a Senior Automation Engineer skilled with Python - please read on Based in San Jose, CA (near the Westfield Valley Fair), we're a mid-sized security company (100 people) with recent funding on a mission to ensure the security of many global organizations. Our solution software is configurable for both local and multinational organizations and has evolved into the lightest, most scalable endpoint solution in the world. Top Reasons to Work with Us 1. You'll be working with the latest backend frameworks/libraries 2. Your day to day programming duties will play a huge role in our overall company success, your work will be helping keep enterprise companies around the globe secure 3. We've got a really cool office space in a great location - literally in the middle of tons of restaurants and shops. What You Will Be Doing - Testing of Windows/OSx/Linux Collector - Testing Linux Clustered Server Solution - Testing interoperability with third-party products - Developing and executing manual and automated test cases - Participating in technical discussion and providing feedback from QA point of view - Understanding the existing automated test framework and enrich it as needed - Being able to create test automation from scratch. What You Need for this Position - 5 years working experience - BSCS or related - Python (Flask / Django) - AWS - Linux Bonus points for: - Telecom / Networking Protocols - Virtualization tools like Virtual Box, VMWare ESXi - Knowledge of and security tools, and vulnerability scanners - Powershell / Shell - Big Data: Spark - Selenium What's In It for You - HUGE room for career growth, we promote upward movement. - You work will be combating cyber fraud/hacking. - Great office location, plenty of things to do and places to eat on your lunch break / after work. - We're a leading company, with a global presence, fun office environment with very sharp engineers.So, if you are a QA Automation Engineer local to the San Jose area - please apply today Applicants must be authorized to work in the U.S.Please apply directly to by clicking 'Click Here to Apply' with your Word resume Looking forward to receiving your resume and going over the position in more detail with you. - Not a fit for this position? Click the link at the bottom of this email to search all of our open positions. Looking forward to receiving your resume CyberCoders CyberCoders, Inc is proud to be an Equal Opportunity Employer All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, protected veteran status, or any other characteristic protected by law. Your Right to Work - In compliance with federal law, all persons hired will be required to verify identity and eligibility to work in the United States and to complete the required employment eligibility verification document form upon hire. Copyright 1999 - 2019 . CyberCoders, Inc. All rights reserved. - provided by Dice Python, Automated Testing, Powershell / Shell, Networking (TCP/IP), AWS, Virtualization, Selenium, Django / Flask, Linux - Python, Automated Testing, Powershell / Shell, Networking (TCP/IP), AWS, Virtualization, Selenium, Django / Flask, Linux
Company Description EPM Scientific is a global specialist recruitment company working exclusively in the Life Sciences industry. As an industry expert we understand that the ongoing changes within ...jobs by
El Segundo,California,United States 6B1DP4 Employer Defense Space & Security seeks Senior Digital ASIC/FPGA Design Engineers to support the Satellite Capabilities organization and multiple satellite product lines based in El Segundo, CA. Position Responsibilities: Utilize high-level architectural documentation along with algorithm description and implement DSP functions for functions such as decimation, interpolation, general filtering, up-down conversion, digital beamforming, and channelization. Develop mathematical models in SystemVerilog to verify design implementation and develop and run scripts and Make files. Leads analysis of customer and system requirements and development of architectural approaches and detailed specifications for various electronic products. Leads development of high-level and detailed designs consistent with requirements and specifications. Leads reviews of testing and analysis activity to assure compliance to requirements. Identifies, tracks and statuses technical performance measures to measure progress and ensure compliance with requirements. Leads activities in support of Supplier Management with make/buy recommendations and other technical services. Coordinates engineering support throughout the lifecycle of the product. Plans research projects to develop concepts for future product designs to meet projected requirements. Works under minimal direction. Employer is the world's largest aerospace company and leading manufacturer of commercial airplanes and defense, space and security systems. We are engineers and technicians. Skilled scientists and thinkers. Bold innovators and dreamers. Join us, and you can build something better for yourself, for our customers and for the world. This position must meet Export Control compliance requirements, therefore a "US Person" as defined by 22 C.F.R. SS 120.15 is required. "US Person" includes US Citizen, lawful permanent resident, refugee, or asylee. Basic Qualifications (Required Skills/Experience): 5 or more years of experience in Digital ASIC design or FPGA verification. Experience with ASIC development including architectural definition, detailed design implementation using SystemVerilog, and functional verification using SystemVerilog. Experience with design architecture and detailed specification generation. Preferred Qualifications (Desired Skills/Experience): Knowledge and competency of UVM. Thrive in working within a fast-paced environment and work well in a team of ASIC/FPGA engineers and Subsystem engineers. Demonstrated history of 1st pass success with ASIC/FPGA designs. Typical Education/Experience: Degree and typical experience in engineering classification: Bachelor's and 9 or more years' experience, Master's with 7 or more years' experience or PhD with 4 or more years' experience. Bachelor, Master or Doctorate of Science degree from an accredited course of study, in engineering, computer science, mathematics, physics or chemistry. ABET is the preferred, although not required, accreditation standard. Yes, 10 % of the Time Space and Launch Individual Contributor No No Standard United States; The Employer Company Department: Engineering - provided by Dice Aerospace, Algorithm, Analysis, Architecture, ASIC, Development, DSP, Lifecycle, Management, Mathematical, Mathematical Models, Physics, Research, Scripts, Security, Specification, Testing
Bachelors of Science degree in biological science, chemistry or related field Company Description Founded and headquartered in Scottsdale, AZ, Concentric Healthcare Solutions specializes in health ...jobs by
Hyundai Kia America Technical Center, Inc. (HATCI) is currently looking for Audio/Advanced Technology Engineer for our Chino, CA location that will: Investigate quality issues on Hyundai or Kia vehicles responding to requests from registered projects resulting from Warranty claims or sudden increase in parts orders. Lead and support audio/navigation/telematics audits with affiliated Hyundai and Kia companies. Assist on evaluating Advanced Driver Assistance Systems (ADAS) and integration with audio/navigation head units. Evaluate Smartphone Apps that integrate with vehicle functions. Conduct field or on-site investigations and subjective and/or objective evaluations during driving to attempt to duplicate conditions or concerns. Collect and record data: analyze data and diagnose root cause. Recommend methods of resolution - field fixes or countermeasures. Create Technical Reports on investigations, analysis and recommendations for Korea R&D and Quality teams. Provide technical support for quality-related meetings and product evaluation programs with affiliated Hyundai and Kia companies. Provide Engineering Support to dealers for non-fixable problems by performing root cause analysis and providing methods of resolution. Identify major quality problems, breakdown to systematic areas and provide Engineering analysis and research results to provide 'lessons learned' on current and future models. Benchmark competitive vehicles to research differences and improve Hyundai/Kia vehicle systems. Knowledge of GSM, CDMA, UMTS, WCDMA, LTE, 3G/4G/5G, Bluetooth, OTA technologies. Remain current with new technology and competitive products as a means to drive new innovative features and functions. Travel up to 40% of time domestically and internationally. Required Experience: Bachelor Degree in Electrical Engineering 5 years’ experience designing and developing automotive electrical components and systems with a focus on multimedia, navigation, smartphone applications and infotainment systems. 5 years of experience in developing specifications and design verification test plans pertaining to multimedia and infotainment with an emphasis on telematics. Valid Driver’s License and satisfactory driving record Candidates applying for positions with Hyundai Kia must be legally authorized to work in the United States. Verification of employment eligibility will be required at the time of hire. HATCI is an Equal Opportunity Employer including Disabled and Veteran. VEVRAA Federal contractor Experience in telematics hardware and software design preferred. - provided by Dice Electrical Engineer, Evaluation, ADAS
MedNet Professionals is currently seeking a Clinical Laboratory Scientist (CLS) for a contract position in Indio, CA. The LS is responsible to perform laboratory testing following the policies and ...jobs by
We are seeking an outstanding Scientist to join the Small Molecule Analytical Chemistry Group. The Scientist will lead from the bench for the characterization of small molecule drug candidates and new drug modalities. The Scientist will serve as the analytical lead on cross-functional project teams collaborating with colleagues in Chemistry, Formulation, Toxicology, Quality and Regulatory groups. The Scientist will use state-of-the-art techniques such as UHPLC, HRMS, GC, GC-MS, and dissolution technologies to solve complex problems and advance projects. The Scientist is expected to maintain a high level scientific profile both internally and externally in terms of pipeline contributions and scholarly achievements. The successful candidate will accomplish our mission through clear communication, innovation, leadership, teamwork and creative problem-solving. Who You Are PhD in Analytical Chemistry, Pharmaceutical Science, or a related discipline with 0-5 years of industry experience. Outstanding record of innovation and success in multiple projects over the course of their graduate, post-doctoral and/or industrial career with a sustained publication record. Candidates must have a strong fundamental knowledge of analytical chemistry and organic chemistry and be able to apply it to development of small molecule and peptide drugs. Knowledge and experience of dissolution, biopharmaceutics and pharmaceutics is preferred. Hands-on experience and in-depth understanding of modern chromatography and other core analytical techniques are required. Have advanced problem solving skills, the ability to think strategically and have sound scientific judgment. Have the potential to augment scientific and strategic competencies as your career grows to support evolving therapeutic platforms. Ability to take initiatives, provide strategic input, solve problems, and ability to interact, learn and eventually lead in a CMC/cross functional environment. Have potential to supervise co-workers and develop people. Have excellent communication skills, both orally and in writing.
Client is seeking a diligent and motivated scientist to join the Molecular & Cell Biology (MCB) group in San Diego. * This position will provide support for assay development and drug discovery ...jobs by
We are currently looking to recruit for Full-Time Clinical Lab Scientists to work in State Correctional Facilities across California. Full Time Clinical Laboratory Scientist in Delano, CA - State ...jobs by
Facebook Reality Labs is dedicated to the research and development required to bring virtual and augmented reality to billions of people around the world. We are looking for a Research Scientist with expertise in neuroimaging to join our BCI team in Menlo Park, CA. In this role, you will design experiments and analyze neuroimaging data to develop state of the art brain-computer interface (BCI) applications for use in virtual and augmented reality systems. Our researchers will have opportunities to collaborate with academic institutions and publish in peer-reviewed journals. Our projects take advantage of internal engineering resources (i.e., mechanical, electrical, optical, and software) to develop neural interface technologies not available commercially. We want people who work well across disciplines, and are excited to work in new technology areas. RESPONSIBILITIES Apply state of the art methods for processing non-invasive neuroimaging data to develop state of the art brain-computer interface (BCI) applications for use in virtual and augmented reality systems Work closely with team members to develop experimental and analytical designs, carry out project plans, and document results for demonstrations and/or academic publications Collect, analyze, and manage large and/or complex neuroimaging datasets MINIMUM QUALIFICATIONS PhD in neuroscience, biology, statistics, physics or related discipline 4 years experience in analyzing neuroimaging data, e.g. fMRI, diffuse optical tomography 2 years experience with a modern statistical programming language, e.g. Python, Julia, R 2 year experience with neuroimaging software tools, e.g. SPM, FreeSurfer, PyCortex Demonstrated experience in design of human experiments Demonstrated experience in applied signal processing PREFERRED QUALIFICATIONS Demonstrated experience applying machine learning to imaging data, e.g. multi-variate pattern analysis, hyperalignment, encoding and decoding models Demonstrated experience in simulation and analysis of diffuse optical tomography applied to detection of functional brain activity Industry experience in software engineering, including use of source control, unit testing, software containers, and continuous integration Experience with hardware (e.g. DAQs, microcontrollers) Experience with Bayesian modeling tools and methods
The Clinical Laboratory Scientist must be able to work efficiently and independently in maintaining quotas and accuracy in benchwork. Qualifications: * California Licensed CLS Generalist / Medical ...jobs by
SUMMARY: Provide Lead responsibilities within the Pharmacy department at Highland Hospital. Provide supervision and functional direction to pharmacist and non-pharmacist employees in an Inpatient or Outpatient Pharmacy setting. Ensures compliance with State & Federal laws, regulations, and standards regarding the provision of pharmaceutical services, and Divisional Pharmacy objectives, policies and procedures. Assists the Pharmacy management team with the development and implementation of strategic initiatives; performs other duties as required. DUTIES & ESSENTIAL JOB FUNCTIONS: NOTE: The following are the duties performed by employees in this classification. However, employees may perform other related duties at an equivalent level. Not all duties listed are necessarily performed by each individual in the classification. 1. Assists the pharmacy management team to define performance objectives and metrics for the department and assess the level - of competence of staff. 2. Assists with staff development programs for training new employees and continuous retraining of existing staff. 3. Communicates new policies, procedures and regulatory hospital matters to the staff and provides for the safety of the staff. 4. Coordinates the duties and assigns daily work assignments of all pharmacists/technicians; orients and trains new pharmacy staff including interns and students as per hospital policies and procedures. 5. Coordinates with the Pharmacy Services Coordinator of support services for the department. Maintains an orderly workflow for all medication dispensing activities in the Hospital. Ensures timely deliveries of all medications. 6. Is registered with California Board Of Pharmacy as the pharmacist in charge (PIC) and responsible for Pharmacist in Charge responsibilities in accordance with the California Pharmacy laws; by ensuring compliance with all laws and regulations governing the operation of their respective pharmacy. 7. Maintains and ensures that the standards of the department are maintained and are within regulatory guidelines. 8. Maintains established procedures concerning quality assurance, security of controlled substances, and disposal of hazardous waste drugs. 9. Maintains high standards within the department and translates pharmacy policies and procedures into the daily operation of the pharmacy in accordance with regulatory agencies. 10. May provide functional supervision to professional, paraprofessional, and support staff in their respective pharmacy, including training, assigning duties, and providing input for performance evaluations. 11. New program/project development: In conjunction with the pharmacy management team to determine feasibility of new services and implements changes in programs/services. 12. Promotes effective working relationships and works effectively as part of a department/unit team inter and intra departmentally to facilitate the departments/units ability to meet its goals and objectives. MINIMUM QUALIFICATIONS: Education: Doctor of Pharmacy required. Advanced degree or approved American Society of Health-System Pharmacist residency preferred. Education: Responsible for self-continuing education by attending conferences, meetings and seminars. Is registered with California Board Of Pharmacy as the pharmacist in charge (PIC). and responsible for Pharmacist in Charge responsibilities in accordance with the California Pharmacy laws; by ensuring compliance with all laws and regulations governing the operation of their respective pharmacy. Minimum Work Experience: Three to five years of hospital pharmacy experience or management experience in either inpatient or outpatient setting. Required Licenses/Certifications: Possession of a valid pharmacist license to practice in California. Is registered with California Board Of Pharmacy as the pharmacist in charge (PIC). and responsible for Pharmacist in Charge responsibilities in accordance with the California Pharmacy laws; by ensuring compliance with all laws and regulations governing the operation of their respective pharmacy.
... Life Science CRO, but to be a pharmaceutical alliance partner. With a team of over 2000 experienced scientists, hundreds of western-trained pharmaceutical industry leaders, and experienced ...jobs by
Associate, Regulatory Affairs CMC III 9 Months San Rafael, CA Duties This position focuses on the management of CMC regulatory activities for an enzyme substitution therapy program for domestic and international regulatory affairs. The role involves working closely with in-house CMC teams, partners, contract manufacturing organizations, and global health authorities to ensure rapid review and approval of the CMC portions of marketing applications, amendments, supplements/ variations, and other CMC-oriented filings. Expertise with biologics and/or drug/biologic/device products is strongly preferred. This position is also responsible for obtaining and interpreting CMC regulations and guidance and providing regulatory advice to technical operations departments. Strong communication and management skills are required. Oversee planning, preparation, and submission of the CMC sections of marketing applications globally. Ensure that the sections are accurate, complete, well-written, and meet all relevant country-specific requirements. Develop excellent relationships with internal functional groups, contract manufacturing organizations, and partners. Researching and interpreting global CMC regulations and providing regulatory guidance to the Quality, Manufacturing, Process Development and other functional groups. Skills: Excellent organization skills. Attention to detail. Understanding of ICH guidances and CMC regulations. Education: 5 Years Experience with Bachelor’s degree in chemistry, biology, biochemistry or related field. - provided by Dice ICH guidances , CMC regulations
Bachelor of Science or a Master's Degree * Experienced working in a pharmaceutical or biotech company performing biologic assays for characterization of proteins required * Proven experience with ...jobs by