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Waltham

497 💼 Other Jobs / Employment in Waltham, MA

Director, Clinical Operations - Waltham

newabout 16 hours ago
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Radius Health Radius Health is an equal opportunity employer.EEO/Disabled Individuals/Veterans.If you need assistance and/or a reasonable accommodation due to a disability during the application or the recruiting process, please send a request to [email protected] here to navigate to the “EEO is the Law” poster.Click here to navigate Radius Health’s Pay Transparency Policy.US-MA-Waltham Job ID 2018-1840 # of Openings 1 Category Clinical Dev - Dept Overview The Director, Clinic

Director, GCP Quality Assurance - Waltham

new1 day ago
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US-MA-Waltham Job ID 2019-1893 # of Openings 1 Category Quality - Dept Overview The Director GCP, Quality Assurance, will have the responsibility to serve as a subject matter expert to ensure that all quality and regulatory compliance related to GCPs, pharmacovigilance, and other related activities performed by Medical/Clinical Departments.The incumbent will provide support and promote collaboration to ensure all systems, processes and their outcomes are compliant with GCP guidelines, and appli

Home Health Care Registered Nurse - Waltham

new1 day ago
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Supplemental Health Care is partnering with a Home Health facility in Waltham, MA to provide an RN. Job Description: The Home Health Registered Nurse will provide care for med-surg, high-acuity patients in their home settings. The Home Care RN will visit 4-6 patients daily, covering an area of 2-3 towns. The nurse will provide care on a wide range of med-surg clinical needs: vent care, trache care, PICC lines management, catheter care, feeding tube management, wound care, etc. The VNA RN will document all treatments and assessments in accordance with OASIS guidelines using an EMR system. This Home Health position is perfect for any RN who values one-on-one time with patients, and for the nurses who love to be on the road. Job Details: Coverage Area: (RN will be assigned 2-3 towns to cover) Type: All positions start as 13-week Contracts Shift: M-F, 8A-5P Hours: 40/week Patient Visits: 28-32/week Start: ASAP Compensation: $40-44 per hour If you are a Registered Nurse and would like more details, please call Ellen MacDowell at 857-302-2002, pm or email me at emacdowellshccares.com RN, MA License BLS 2 years experience as a Registered Nurse with 1 year of experience in home health

CyberArk PAM Consultant

new1 day ago
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Softpath is an award winning national consulting services with 18 Years of industry experience. We support Fortune 50 clients in 20 verticals including Pharma, Financial, Healthcare, IT, Retail, Telecom, Mfg., plus StateFederal Agencies. Softpath helps customers consistently and cost-effectively plan and deliver high-quality projects and business results. Title CyberArk PAM Consultant role Location Waltham, MA Duration 1 year contract postiion Position Description Our client is a Large Utilities Company located in the Waltham, MA area that is looking for a CyberArk PAM Consultant to fill a 1 year contract opening. Required Skills A minimum of 7 years plus experience in developing, implementing or architecting information systems. A minimum of 5 years of experience with technical architecture experience integrating identity management, access management and access governance software into clients' infrastructure and applications. A minimum of 5 years plus experience with installation, integration and deployment of one of the following PAM product CyberArk in a client environment. Responsible for planning, scoping, deploying and integrating Privileged Account Management Solutions CyberArk EPV and CA PAM Responsible for rolling out PAM solution with expertise in integrating disparate systems Engineers business processes and solutions to ensure that PAM services perform per defined processes, meet defined policies and comply with applicable information security requirements Identity Management familiarity in one or more of the following areas Single Sign On Identity Federation Enterprise Directory Architecture and Design including directory schema, namespace and replication topology experience Resource Provisioning Identity Access Governance including Role based access control, access request and certification Desired Skills (not required but candidate will have exposure to these skills in this role) Understanding of fundamental cloud computing concepts Experience with Information Assurance concepts and processes Knowledge of and experience with security regulations, standards, and processes Java and Identity and Access Management Excellent communications skills and ability to interact with the client daily Strong technical writing skills Willingness to train others and lead engagement teams Fundamental understanding of software, computer, and network architectures. Expertise in Security Architecture, vulnerability management program management, operational activities, and technical toolsets Proficiency in one or more of the following security technologies SIEM, Endpoint, Firewalls, Proxy, Endpoint, and general networking background Working knowledge of security governance, compliance frameworks, and technical hardening standards (e.g. PCI, HIPAA, CIS, NIST, etc.) Bachelor of Science in Computer Science, Information Systems Management of Similar Field Consulting responsibilities Working with a project manager to organize client and internal kick-off meetings Taking detailed notes during meetings and identifying project risks Deployment of CyberArk Suite of products that include Vault Privilege Session Manager AIM PTA Performing discovery audits and presenting findings to client management Creation of project deliverables Contributing the Center of Excellences (COE) improvement by making suggestions Additional Requirements Candidate must be able to pass a background check and drug test Thanks Regards, Dharma Teja Email dharmasoftpath.net mailtodharmasoftpath.net Direct 678-783-7397

jobs byAdzuna

Contract Sr. Trade Compliance Specialist - Waltham

new1 day ago
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JOB TITLE: Contract Sr. Trade Compliance Specialist in Waltham, MA (3 Months) Pay Rate: $33/hr to $37/hr Responsibilities: Senior Trade Compliance Specialist will be responsible to ensure all import and export regulations are properly followed. Review and improve trade compliance processes of company. Support all business divisions with trade compliance questions and identify cost savings wherever possible. 1. Manage and maintain USA Trade Compliance (Import/Export) programs, policies and groups to ensure compliance to all relevant rules and regulations of the region and Corporate policies; 2. Manage and maintain reports and metrics pertaining to various elements of import/export processes, review import/export data and files for reporting; 3. Assist with strategic projects to improve efficiency, compliance, and cost reduction initiatives; 4. Work with all business divisions to ensure proper HS coding, ECCN numbers, country of origin and other import and export requirements are met; 5. Secure export licenses and import/export rulings whenever necessary; 6. Work with overseas affiliate distributors to ensure proper export compliance process is being followed; 7. Identify training needs, develop and provide training pertaining to import/export requirements and manage relationships with customs brokers and freight forwarders; 8. Ensure our databases are updated with proper information; 9. Perform other related duties as assigned. Qualifications: Education: • BS Business Degree/Business Administration/Supply Chain; • 5-7 years of experience in Import/Export Regulations knowledge a plus; experience will be substituted for degree. Experience: • Provide regulatory interpretation and guidance in the following areas: Import/Export Control Classification, Export Documentation, Tariff Classification, Duty Drawback and Recordkeeping • Proficient with the Microsoft Office platform • Knowledge of U.S. Trade Regulations. Skills: • Excellent verbal and written communication skills • Must be a highly organized, self-managed individual who works independently with minimum supervision and the ability to work in fast paced environment. • Ability to analyze technical data. Competencies: • Ability to interact with fellow employees and outside contacts. • Ability to plan, organize and set priorities • Ability to manage multiple priorities and multiple tasks simultaneously with strong attention to detail. • Perform other incidental and related duties as required and assigned. If interested, please let me know immediately. Kelley Arzola | Professional Technical Recruiter | Kelly Services - e-Accounts division Kela807kellyservices.com ( 630-424-3601 www.kellyservices.com Why Kelly ® ? At Kelly Services ® , we work with the best. Our clients include 95 of the Fortune 100 ™ companies, and more than 70,000 hiring managers rely on Kelly annually to access the best talent to drive their business forward. If you only make one career connection today, connect with Kelly. About Kelly Services ® As a workforce advocate for over 70 years, we are proud to directly employ nearly 500,000 people around the world and have a role in connecting thousands more with work through our global network of talent suppliers and partners. Revenue in 2017 was $5.4 billion. Visit kellyservices.com and connect with us on Facebook , LinkedIn and Twitter . Kelly Services is an equal opportunity employer including, but not limited to, Minorities, Females, Individuals with Disabilities, Protected Veterans, Sexual Orientation, Gender Identity and is committed to employing a diverse workforce. Equal Employment Opportunity is The Law.

Director, GCP Quality Assurance

new2 days ago
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US-MA-Waltham Job ID 2019-1893 of Openings 1 Category Quality - Dept Overview The Director GCP, Quality Assurance, will have the responsibility to serve as a subject matter expert to ensure that all quality and regulatory compliance related to GCPs, pharmacovigilance, and other related activities performed by Medical/Clinical Departments. The incumbent will provide support and promote collaboration to ensure all systems, processes and their outcomes are compliant with GCP guidelines, and applicable international and national standards, regulations and guidelines. Act as a Radius representative during regulatory agency inspections and vendor audits. Responsibilities Assists in the implementation of GXP compliant procedures and operations to ensure a robust quality management system for both the conduct of clinical studies as well as prepare the company to successfully commercialize pharmaceutical products Proactively provides GCP QA support to Clinical Operations based on analysis and interpretation of updates to GCP regulations to assure best Clinical/QA practices Assists with the organization, preparation, coordination, and documentation of regulatory inspections Schedules and conducts Good Clinical Practice (GCP) Audits of systems and processes related to clinical operations, pharmacovigilance and clinical drug development. Provides GCP compliance oversight of internal systems and processes as well as those of CROs, Vendors, and Clinical Investigator Sites. Reviews and provides input to clinical documentation (protocols, study reports, IB) Develops and measures quality metrics to drive consistent quality standards throughout the organization. Qualifications Bachelor's degree is required with 7-10 years' experience and 5 plus years' experience in Quality Systems related to GCP. Demonstrate ability to effectively communicate and influence the outcomes of the decision making process Analytically strong with practical knowledge of how to identify key performance metrics for quality indicators to set targets for maintaining a state of control while identifying areas for improvement. Extensive experience auditing clinical CRO's, clinical sites and investigator sites. PM18 PI108356522

jobs byAdzuna

Head of Clinical Operations

new2 days ago
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Radius Health Radius Health is an equal opportunity employer. EEO/Disabled Individuals/Veterans. If you need assistance and/or a reasonable accommodation due to a disability during the application or the recruiting process, please send a request to HRconnectradiuspharm.com. Click here to navigate to the “EEO is the Law” poster. Click here to navigate Radius Health’s Pay Transparency Policy. US-MA-Waltham Job ID 2018-1848 of Openings 1 Category Clinical Ops - Dept Overview The Sr. Director, Clinical Operations is responsible for leading and driving clinical trial operations for Radius' current and future programs. This role will oversee the Radius Clinical Operations team to ensure all assigned operational trial deliverables across programs are completed according to timelines budget, operational procedures, quality standards, SOPs and business guidelines. This individual will need expertise in successful planning, implementation, and delivery of clinical operations strategy, plans and study execution. The Sr. Director, Clinical Operations will also be responsible for managing and supporting vendor/CRO relationships and activities including negotiations and performance evaluations. This individual will be a member of the R&D leadership team and will be a significant contributor to the overall R&D strategy at Radius. Responsibilities Provide functional leadership for clinical operations, including hiring, training, staff assignments, coaching, mentoring and performance management in a matrix environment Set department goals and objectives which align with broader company goals Provide strategic and tactical input into integrated clinical development strategy and timelines Develop clinical operations strategy including risk management and contingency planning Build collaborative relationships with key internal stakeholders to facilitate the planning and execution of clinical trials Guide the clinical operations execution activities of all clinical trials Establish and maintain strategic partnership with Radius CROs and clinical vendors to include vendor governance and identification and resolution of performance issues Ensure all clinical trials are executed per key metrics (timelines, budget, operational and quality standards [ICH/GCP/SOPs]) Maintain procedures to verify the accuracy and timeliness of trial information in all trial databases and tracking systems Contribute to global regulatory submissions (FDA, EMA, Health Canada and other governing regulatory bodies) Oversee the clinical operations aspects of cross functional work processes involving medical writing, legal, finance, quality assurance, pharmacovigilance, biometrics, program management, regulatory, pharmaceutical sciences, IT, medical affairs, translational science and clinical science Drive the creation of clinical operations Standard Operating Procedures (SOPs), systems, and processes Foster a highly collaborative culture and serve as a leadership role model within the company and with external stakeholders Qualifications 12 years of clinical operations experience in a pharmaceutical, biotech and/or contract research organization (CRO) setting; including management of a CRO 8 years supervisory experience, 5 years direct project/trial management experience and 4 years in leadership role Requires a BS in the health or life sciences or equivalent Osteoporosis or oncology experience is preferred Analytical thinker with excellent problem-solving skills and the ability to adapt to changing priorities and deadlines Strong leadership, collaborative and interpersonal skills Proven ability to build strong relationships with CROs/vendors Excellent computer skills (Microsoft Office Suite, Project, Visio, Electronic Data Capture and Trial Master File Systems) Global Clinical Trial Experience and the ability to support more than one clinical trial is preferred Experience working independently and in a team environment, being flexible and adapting in a changing environment Ability to travel up to 30% Work Environment: The work is performed in a typical office environment with heavy computer duties. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. The noise level in the work environment is usually quiet. Frequent travel required. The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this position. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this position, the employee is regularly required to use hands to type, handle paperwork and sort, file or manipulate documents. The employee is occasionally required to stand and walk. The employee must frequently lift and/or move up to 10 pounds and occasionally lift and/or move up to 25 pounds. Specific vision abilities required by this position include close vision, distance vision, color vision peripheral vision, depth perception and ability to adjust focus. PI108356533

jobs byAdzuna

Director, Clinical Operations

new2 days ago
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Radius Health Radius Health is an equal opportunity employer. EEO/Disabled Individuals/Veterans. If you need assistance and/or a reasonable accommodation due to a disability during the application or the recruiting process, please send a request to HRconnectradiuspharm.com. Click here to navigate to the “EEO is the Law” poster. Click here to navigate Radius Health’s Pay Transparency Policy. US-MA-Waltham Job ID 2018-1840 of Openings 1 Category Clinical Dev - Dept Overview The Director, Clinical Operations will provide oversee the execution of clinical trials within the development programs. The incumbent will serve as the governance contact for the CRO and clinical vendors, will ensure that all assigned operational trial deliverables are met according to timelines, budget, operational procedures, quality standards, SOPs and business guidelines. Responsibilities Provides strategic input to the clinical development plan Develops the operational plans for trials within the assigned development program(s) Oversees trial execution team to ensure delivery of clinical trial within budget and agreed upon timelines Identifies and/or anticipates operational risks and mitigation plans across trials within the development program and escalates issues to senior management as necessary Manages the quality of work performed by direct reports (i.e. AD, CTM, CRA, and CTC) through regular review and evaluation of work product. Acting as a coach and mentor. Serves as the relationship manager for CRO/Vendors and is a member of the joint oversight committee Reviews CRO/Vendor agreements and negotiates the performance metrics to be outlined within the agreements Contributes to Global clinical / regulatory submissions May perform periodic visits to sites and/or vendors to assess progress and compliance Presents status reports of operational execution activities to senior management Ensure clinical trials maintain an inspection readiness state throughout the lifecycle of the trial Qualifications 12 years of clinical operations experience in a pharmaceutical, biotech and/or contract research organization (CRO) setting; including management of a CRO. 7 years supervisory experience, 5 years direct project/trial management experience and 2 years in leadership role Strong collaborator with excellent communication skills; "Can do" attitude. Requires a BS in the health or life sciences or equivalent. Oncology experience is highly preferred. Experience with trial master file organization, regulatory documents, inspection preparation/readiness (site and Sponsor) required. Good working knowledge of the international conference on harmonization (ICH) and good clinical practice (GCP) guidelines and other applicable regulatory guidelines required; basic statistical knowledge preferred. Excellent computer skills (Microsoft Office Suite, Project, Outlook; Electronic Data Capture and Trial Master File Systems). Global Clinical Trial Experience and the ability to support more than one clinical trial is required. Work Environment: The work is performed in a typical office environment with heavy computer duties. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. The noise level in the work environment is usually quiet. Frequent travel required. The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this position. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this position, the employee is regularly required to use hands to type, handle paperwork and sort, file or manipulate documents. The employee is occasionally required to stand and walk. The employee must frequently lift and/or move up to 10 pounds and occasionally lift and/or move up to 25 pounds. Specific vision abilities required by this position include close vision, distance vision, color vision peripheral vision, depth perception and ability to adjust focus. PI108356535

jobs byAdzuna

Senior Systematic Reviewer (Research Associate III) Meta Research ( Waltham MA or London UK)

new3 days ago
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Senior Systematic Reviewer (Research Associate III) - Meta Research ( Waltham MA or London UK)**We are looking to fill this role in our Waltham , MA or

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Operations Paralegal - Temp / Contractor - $25.00 per hour

new3 days ago
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Waltham, MA Term: 6-month contract to start Pay Rate: $20-25 per hour W2 (without benefits) We have ... Maintain complete, accurate and up-to-date records of contracts, correspondence and other matters ...

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Director of Artwork and Package Design

new4 days ago
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The Director of Artwork and Package Design is a strategic leader who is driven to deliver meaningful design solutions for Alkermes’ proprietary product portfolio. This position is responsible for leading the artwork/labeling design activities as well as delivering best practice packaging concepts to the business. This work requires a creative, conceptual, and strategic thinker who is experienced and confident in leading a talented team that manages labeling and package design, and support documentation for both commercial and clinical products within a pharmaceutical environment. The ideal candidate takes initiative and has the ability to influence and manage multiple projects, while delivering a high level of creative standards. This role has responsibility for identifying projects and driving the development of timelines with design team members and cross-functional partners. This individual will manage the security efforts for anti-counterfeiting measures, support clinical packaging & labeling and champion labeling through the review and approval process as well as implementation. The Director of Artwork and Package Design will interact cross-functionally with members of Regulatory Affairs, Commercial, Medical Affairs, Quality and others to develop, review, implement and provide systems support of GMP labeling and will integrate complex programs working within a cross functional partnership. This position requires a motivated team player who can align with and support the Alkermes business principles, mission, objectives, and goals. Essential Areas of Responsibility: Lead and partner in the process for creation, approval, and implementation of commercial and clinical printed labeling and components in collaboration with various functions Provide tactical and strategic guidance or recommendations to product labeling teams regarding placement and regulatory requirements for global packaging component labeling content and design Developing and directing branding initiatives in alignment with corporate goals Developing consistent and effective design standards that establish a "design face" for the company Lead the development and maintenance of work practices, templates, and associated documents relating to the artwork, labeling and package design function Own the phrase library and assist in the language translation process Manage internal documentation requirements including change controls, specifications, item code creations, pertinent SOPs and artwork libraries.Support document management, change control and other process requirements Process and prepare Printed Labeling required for submission Establish creative and production processes for packaging artwork execution Manage technical requirements of labeling to ensure it meets the technical standards/specifications for GS1, the contract manufacturer organizations (CMO)’s, printer, etc. Prepare and manage annual budgets Coordinate and manage the change control process for all GMP labeling and package design modifications. Employ measures for counterfeit protection to implement overt and covert anti-counterfeiting technologies. Partners with marketing, consumer research and CMC teams to develop package designs that inspire consumers and provide product protection Support qualification and/or validation of systems or equipment necessary for graphics or labeling Coordinate review, obtain internal approvals and ensure labeling follows Quality system requirements, GMP and applicable domestic, international regulatory requirements and anti-counterfeiting provisions Oversee generation of final proof copy/transparency proof and creation of commercial print-ready artwork files Serve as the primary information base for all issues related to commercial product labeling/printed components Support Regulatory Affairs in packaging responses to Health Authorities Ensure tracking of all versions, specifications and coding for each labeling component for all GMP labeling Accountable for Labeling Design process and metric tracking Act as a change leader to drive the continued development and transformation of artwork and package design systems and related strategy to meet the needs of the growing business Identify continuous improvement and best practice projects, prepare and execute project plans to deliver identified improvements related to service, cost and effectiveness Build and lead a team of professionals through succession planning, employee selection, coaching and development, and performance management activities Maintain/enhance job knowledge and understanding of industry trends by participating in educational opportunities or conferences; use of professional publications; alignment with professional organizations, maintaining personal networks. Enhance department and organization reputation by accepting ownership for accomplishing new and different requests; exploring opportunities to add value and enhance customer satisfaction Represent the organisation externally as required to deliver the responsibilities of the role Competencies: The candidate will be a leader, with broad awareness of best practices in artwork design and management as well as packaging design. Self-directed with an ability to network Propensity for building, mentoring, developing, leading and managing teams with enthusiastic and effective personnel management skills Excellent interpersonal and collaboration skills including the ability to make connections, build relationships and influence at all levels Analytical and problem solving skills with record of innovation and results Strong business acumen and the ability to understand current technology trends and their impact on business strategy Extensive stakeholder management experience Capability to provide a strategic vision for the Artwork Management and Packaging Design function Demonstrates flexibility adapting to external environmental influences through development of new strategies and tactics Ability to identify processes needing improvement, coordinate change and implement effectively through leadership skills A holistic thinker who can look enterprise-wide to integrate and streamline systems Ability to make decisions at the project team level and properly escalate those decisions that cannot be resolved Ability to work with cross functional teams and multiple projects simultaneously Excellent communication & listening skills, speaks clearly and persuasively in positive or negative situations Responds well to questions, demonstrates presentation skills, participates in meetings Keen attention to detail and accuracy Maintains a high level of package design related knowledge, including current trends, methods and processes Continues professional development by stretching understanding of design, execution processes, industry best practices and related information Education & Experience Requirements: Bachelor’s degree in Graphic Design, Packaging Engineering or related field 12 years of experience in artwork design, packaging development or closely related Minimum 5 years in life sciences industry experience; experience in Pharmaceutical/Biotech an advantage A minimum of 6 years’ experience in people management/leadership roles Experience in leading and managing design leaders, cross-functional teams, supplier relationships, and deep experience training teams on how to effectively harness the power of design thinking and design excellence across the organization Established track record with evidence of excellent people management experience, project management, problem solving, collaboration, leadership and communication skills Specific Functional Software expertise (e.g. Abode Design Suite, Acrobat plus QuarkXpress; Project Management Software; Agile; or others; etc.) Experience working within a regulated industry with quality management system requirements is essential including general knowledge of GMP and CFR’s Excellent knowledge of labeling regulations and guidances Proven track record of delivering business and operational benefit in a global complex/decentralized environment Positive attitude and strong interpersonal skills required to effectively address problems and interface with other functional areas of the company. Strong understanding of budget development and spend management Physical Demands and Work Environment: Travel domestic and international – up to 20% In-house position based in Waltham, MA

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Class A CDL Drivers: Be Your Own Boss with Lease Purchasing! ( Waltham , MA )

new4 days ago
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…EVERY NIGHT! BECOMING YOUR OWN BOSS HAS NEVER BEEN EASIER. The RoadOne Lease Purchase Program puts CDL Class A Truck Drivers behind the wheel of your very own driving

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Senior Systematic Reviewer (Research Associate III) Meta Research ( Waltham MA or London UK)

new4 days ago
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Senior Systematic Reviewer (Research Associate III) - Meta Research ( Waltham MA or London UK)* * We are looking to fill this role in our Waltham , MA or

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Waltham RN/LPN

new4 days ago
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…RNs and LPNs! For patient opportunities North and West of Boston, MA including: Amesbury, Waltham , Concord, Cambridge, Lexington, Newton, Billerica, Burlington,

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Contract Sr. Trade Compliance Specialist

4 days ago
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JOB TITLE: Contract Sr. Trade Compliance Specialist in Waltham, MA (3 Months) Pay Rate: $33/hr to $37/hr Responsibilities: Senior Trade Compliance Specialist will be responsible to ensure all import and export regulations are properly followed. Review and improve trade compliance processes of company. Support all business divisions with trade compliance questions and identify cost savings wherever possible. 1. Manage and maintain USA Trade Compliance (Import/Export) programs, policies and groups to ensure compliance to all relevant rules and regulations of the region and Corporate policies; 2. Manage and maintain reports and metrics pertaining to various elements of import/export processes, review import/export data and files for reporting; 3. Assist with strategic projects to improve efficiency, compliance, and cost reduction initiatives; 4. Work with all business divisions to ensure proper HS coding, ECCN numbers, country of origin and other import and export requirements are met; 5. Secure export licenses and import/export rulings whenever necessary; 6. Work with overseas affiliate distributors to ensure proper export compliance process is being followed; 7. Identify training needs, develop and provide training pertaining to import/export requirements and manage relationships with customs brokers and freight forwarders; 8. Ensure our databases are updated with proper information; 9. Perform other related duties as assigned. Qualifications: Education: • BS Business Degree/Business Administration/Supply Chain; • 5-7 years of experience in Import/Export Regulations knowledge a plus; experience will be substituted for degree. Experience: • Provide regulatory interpretation and guidance in the following areas: Import/Export Control Classification, Export Documentation, Tariff Classification, Duty Drawback and Recordkeeping • Proficient with the Microsoft Office platform • Knowledge of U.S. Trade Regulations. Skills: • Excellent verbal and written communication skills • Must be a highly organized, self-managed individual who works independently with minimum supervision and the ability to work in fast paced environment. • Ability to analyze technical data. Competencies: • Ability to interact with fellow employees and outside contacts. • Ability to plan, organize and set priorities • Ability to manage multiple priorities and multiple tasks simultaneously with strong attention to detail. • Perform other incidental and related duties as required and assigned. If interested, please let me know immediately. Kelley Arzola | Professional Technical Recruiter | Kelly Services - e-Accounts division Kela807kellyservices.com ( 630-424-3601 www.kellyservices.com Why Kelly ® ? At Kelly Services ® , we work with the best. Our clients include 95 of the Fortune 100 ™ companies, and more than 70,000 hiring managers rely on Kelly annually to access the best talent to drive their business forward. If you only make one career connection today, connect with Kelly. About Kelly Services ® As a workforce advocate for over 70 years, we are proud to directly employ nearly 500,000 people around the world and have a role in connecting thousands more with work through our global network of talent suppliers and partners. Revenue in 2017 was $5.4 billion. Visit kellyservices.com and connect with us on Facebook , LinkedIn and Twitter . Kelly Services is an equal opportunity employer including, but not limited to, Minorities, Females, Individuals with Disabilities, Protected Veterans, Sexual Orientation, Gender Identity and is committed to employing a diverse workforce. Equal Employment Opportunity is The Law.

jobs byAdzuna

Head of Clinical Operations

4 days ago
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Head of Clinical Operations Head of Clinical Operations Job Locations US-MA-Waltham Posted Date 2 months ago(1/30/2019 3:23 PM) Job ID 2018-1848 of Openings 1 Category Clinical Ops - Dept Overview The Sr. Director, Clinical Operations is responsible for leading and driving clinical trial operations for Radius’ current and future programs. This role will oversee the Radius Clinical Operations team to ensure all assigned operational trial deliverables across programs are completed according to timelines budget, operational procedures, quality standards, SOPs and business guidelines. This individual will need expertise in s

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Director, Corporate Strategy

5 days ago
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Job Description When you’re part of the team at Thermo Fisher Scientific, you’ll do important work, like helping customers in finding cures for cancer, protecting the environment or making sure our food is safe. Your work will have real-world impact, and you’ll be supported in achieving your career goals. Location/Division Specific Information Group/Division: Corporate Location: Waltham, MA How will you make an impact? The Director of Corporate Strategy will support Thermo Fisher Scientific’s long term corporate strategy development efforts by facilitating the identification of growth drivers and challenges across the Company’s diverse portfolio of businesses. The Director will work collaboratively with colleagues within Strategy & Corporate Development and/or within the businesses and functions to support, help implement, and track key strategic projects that have significant impact on the Company. The Director, reporting to the Vice President of Corporate Strategy, will provide strategic thought leadership and project management on a broad range of topics affecting the Company, including analysis in support of new business initiatives (both organic and M&A related) and cross-divisional initiatives that seek to leverage the scale and depth of Thermo Fisher Scientific. It is essential that this person is able to establish rapport, credibility, trust, and respect throughout the organization, be viewed as a team player, and can work effectively under pressure and with tight deadlines. What will you do? Support the corporate strategic planning process, help manage specific corporate strategy initiatives across the company, and facilitate cross-functional and cross-business projects Support strategy development across Thermo Fishers businesses by working collaboratively with Division and Corporate management Support Divisional strategic planning processes including Board presentations Utilize project management, analytical and decision support skills to lead ‘special projects’ that advance key strategic priorities for the company and/or specific businesses Lead competitive and market analysis for key strategic and M&A diligence projects and draw insights and implications for the company. Present findings and recommendations as appropriate Identify, define, and articulate industry, market, and emerging trends and how they may affect Thermo Fisher’s businesses Evaluate white space opportunities for possible expansion Evaluate market and competitive dynamics as part of M&A diligence projects Act as liaison for relevant strategic initiatives, and help develop and track implementation plans to ensure the right level of focus and discipline Lead special projects to evolve and enhance the Corporate Strategy function and processes How will you get here? Education Masters degree in business, life sciences, or related field 8 years of relevant professional experience, including broad-based experience in strategy and market/financial analysis within a Corporate or Consulting setting; at least 3 years experience at a top-tier management consulting firm (e.g. Bain, McKinsey, BCG) Excellent critical thinking, project management, analytical, communication, presentation skills Not afraid to ‘roll your sleeves up’ and work with details as well as the big picture High level of intellectual curiosity combined with a ‘results-driven’ mindset and high EQ Ability to work effectively with senior executives Highly self-motivated with ability to manage and prioritize multiple projects and initiatives Relevant life science industry experience preferred, but not required Non-Negotiable Hiring Criteria: Masters degree in business, life sciences, or related field preferred 8 years of relevant professional experience, including broad-based experience in strategy and market/financial analysis within a Corporate or Consulting setting; at least 3 years experience at a top-tier management consulting firm (e.g. Bain, McKinsey, BCG) Excellent critical thinking, project management, analytical, communication, presentation skills

jobs byAdzuna

Experienced CDL-A Truck Drivers ( Waltham , MA )

6 days ago
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…CALL NOW TO SPEAK WITH A RECRUITER: (866) - EXCELLENT BENEFITS: Medical /Dental/Vision/Prescription Drug plans 401k Paid Vacation High Tech Equipment Paid Weekly

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Sales Development Associate (Waltham) - 104

10 days ago
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Based in Waltham, MA - $42-45,000 Base / $65,000 OTE Expert level pipeline management * Experienced ... Contribute to the Product, Marketing, Success, and other teams to make the company better Who we ...

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Senior Global Recruiter Human Resources ( Waltham , MA or Bethesda, MD)

13 days ago
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Senior Global Recruiter - Human Resources ( Waltham , MA or Bethesda, MD)Position Overview:Reporting to the Executive Director of Global Recruitment, serves as a

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Senior Global Recruiter Human Resources ( Waltham , MA or Bethesda, MD) - Evidera

13 days ago
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Senior Global Recruiter - Human Resources ( Waltham , MA or Bethesda, MD) Position Overview: Reporting to the Executive Director of Global Recruitment, serves as a

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Senior Director, Global Deal Desk

16 days ago
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Description Title: Senior Director, Global Deal Desk Location: Santa Clara, CA or Waltham, MA Company ServiceNow, the fastest-growing enterprise company over $1 Billion, is changing the way people work. The company was founded on the beach in San Diego in 2004 with the belief that getting simple stuff done at work shouldn’t be so hard. And that the complex stuff should be easier to manage. We envisioned a world where anyone could create workflows that worked for—not against—them. The ServiceNow cloud‑based platform was built to simplify the way work gets done. Today, every enterprise is becoming a technology company, creating unprecedented challenges, opportunities, and complexity. ServiceNow lets them run smarter, faster, better. And it helps people spend their time on work that’s meaningful, not menial. We’re disruptive. We work hard but try not to take ourselves too seriously. We are highly adaptable and constantly evolving. We are passionate about our product, and we live for our customers. We have high expectations and a career at ServiceNow means challenging yourself to always be better. The Role ServiceNow is currently seeking a talented, highly driven Senior Director, Global Deal Desk leader. This critical role is responsible for actively leading and developing a high performing team of deal desk specialists supporting the field in structuring commercially viable, non-standard transactions. This role can be based out of ServiceNow’s Santa Clara, CA headquarters or our Waltham, MA location and is a true value-add partner and business liaison to the field sales organization. Responsibilities: Work cross functionally across stake holder groups; revenue, legal, sales ops, order management, to help facilitate deal approvals/closure Partner with the sales organization to problem solve and structure strategic deals Develop and document play books and models enabling repeatable processes and scale Provide training to the sales team on deal structuring and best practices to increase awareness and accelerate deal velocity Lead initiatives such as development of dashboards, metrics, and system capabilities to gain better visibility into deals Participate in drafting commercial language and terms; build out the non-standard library Actively participate in deal reviews with customers/prospects, sales teams, and management Identify and drive implementation of new tools and process improvements to support growth Cultivate internal relationships with all levels of the sales organization Manage and develop the global deal desk team Perform ad hoc reporting and analysis for management Experience required: 15 years of experience in a global finance, revenue, or deal desk role; software/Xaas experience required BA or BS degree in Business Administration or Finance; MBA and/or CPA preferred 6 years of management experience with a demonstrated ability to manage teams, drive process, and develop talent Experience in negotiating and managing deals in a direct and channel/MSP environment Strong understanding of accounting standards and revenue recognition; working knowledge of 606 a plus A thorough understanding of the sales process and the ability to navigate and progress long, complex sales cycles Strong business acumen with excellent communication skills – verbal and written Adept at business partnering and working with cross functional teams, building meaningful business relationships along the way Self motivated and able to work under pressure; dependable with deliverables and deadlines, able to multi-task Able to adapt to a constantly changing environment; flexibility to work extended hours during peak periods

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Senior Director, Automation and Performance Engineering

16 days ago
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The team is chartered with developing mission critical quality automation and performance driven tools for our cloud offering using cutting edge technologies. You will be involved in leading a team tasked with selection and development of automation tools and frameworks. Team members range in years of experience. As Leader of Automation and Performance team you would be expected to have hands on knowledge of your craft, have a proficient understanding of software life cycle, and grow and mentor your team. “One of the best things about Intralinks from a developer’s standpoint is you will always get to use the newest technology out there. You never get bored.” -Quote from a Principal Applications Developer in our Waltham, MA office. Responsibilities Mentors and manages team members. Sets and determines charter of automation team Engages in discussions with Engineering team and others on the feasibility of the proposed solutions and the time necessary to accomplish the work; Writes detailed design documents describing the approach to be taken and programming details; Assume ownership of automation team deliverables. Sets strategic vision for all automation frameworks. Supports service teams. Prepares related documentation. Responds to and resolves escalated calls for technical assistance received from production support. Manage the delivery of assigned modules on time and budget with high quality Review Requirements and test plans Other duties as assigned. The Projects: We are working on next generation platform on front end as well as backend. Developers will be working on cutting edge automation technologies and frameworks. Your team will be supporting R&D teams and provide automation technologies to test their code. This person will have the opportunity to work on all aspects of test automation frameworks and tools and contribute to the success of the product development. Developers will be involved in Microservices development, component development and deployment. Microservices has become a preferred way of creating enterprise applications. Thanks to its scalability, this architectural method is considered ideal when you have to enable support for a range of platforms and devices. Your team will be using technologies like Selenium, Chef, Puppet, Salt, Ansible, OpenStack, Cucumber, Calabash, jmeter, javascript, dynatrace. You must have solid understanding of these technologies. Required Skills: Proven 5-8 years of Leadership experience Knowledge and experience with application monitoring tools such as Nagios Knowledge and experience with Infrastructure automation tools such as Chef, Puppet, Salt Knowledge and experience with Infrastructure automation tools such as Selenium, Cucumber, Calabash Knowledge and experience with Performance automation tools such as Soasta, jmeter, dynatrace Knowledge and experience with custom restful API Infrastructure automation frameworks such as SoapUI, HP QTP, HttpMaster, Parasoft, vREST Knowledge of Quality and Systems Development methodologies Highly analytical, pro‐active and detail oriented Excellent communication skills and experience working in a multi‐site environment with on shore and off shore team Desired Skills: Experience in designing Automation and implementation for Big data applications Experience with Agile/Scrum methodology a strong plus Experience with some (required) or all (desired) of the following is expected: Hadoop/Pentaho/Vertica/AWS Object Oriented Programming Java SQL Python JUnit, SAM Eclipse, Ant, Git, Maven, XSLT, Ruby on Rails JIRA, Subversion Knowledge of Xcode and Eclipse/Studio.

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20 days ago
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Salary $45,000 with OTE of $65,000 Full Benefits included, based in Waltham, MA Tons of perks and ... the other half you'll generate through classic prospecting techniques, resulting in an average of ...

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about 2 months ago
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AVSS - Audio Visual (A/V) Support Specialist MA (Boston) Boston, MA • 1432 Main St., Waltham, MA ... The candidate will be responsible for the ongoing operation of client conference rooms and other ...

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Senior Systematic Reviewer (Research Associate III) Meta Research (Waltham MA or London UK)

5 months ago
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We are looking to fill this role in our Waltham, MA or London, UK offices The Team Do you have what ... Participate in non-literature based research and consulting activities within other departments (e ...

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