• Senior Regulatory Affairs

    J&J Family of Companies (Boston, MA)
    Senior Regulatory Affairs Specialist - 2406193618W **Description** Abiomed, part of Johnson & Johnson's MedTech, is recruiting for a Senior Regulatory ... a proven track record for growth, integrity and innovation. The Senior Regulatory Affairs Specialist will be responsible for developing strategies to obtain… more
    J&J Family of Companies (06/14/24)
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  • Regulatory Affairs Specialist

    Hologic (Marlborough, MA)
    Regulatory Affairs Specialist 3 San Diego, CA, United States Marlborough, MA, United States **Job Summary** Responsible for regulatory compliance ... engineering with a minimum of 5-8 years direct experience in Regulatory Affairs within an IVD or Drug/Biologics Industry. International experience preferred. +… more
    Hologic (06/15/24)
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  • Regulatory Affairs Specialist

    Philips (Cambridge, MA)
    …As a core member of multiple sustaining and new product development teams, the Regulatory Affairs Specialist will provide timely and valued regulatory ... Provide audit, CAPA and post market regulatory support + Mentor other regulatory affairs personnel within HPM Regulatory **You're the right fit if:** US… more
    Philips (06/27/24)
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  • Regulatory Affairs Specialist

    Olympus Corporation of the Americas (Westborough, MA)
    …is to make people's lives healthier, safer, and more fulfilling.** **Job Description** The Specialist , I - Regulatory Affairs will support the maintenance of ... EU MDR technical documentation and conduct other elements of sustaining Regulatory Affairs including maintaining "state of the art". In addition, this position… more
    Olympus Corporation of the Americas (06/22/24)
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  • Senior Regulatory Affairs

    Philips (Cambridge, MA)
    …role you have the opportunity to** Responsible for influencing department regulatory processes and procedures, developing strategies for worldwide regulatory ... US and EU submissions, and ensuring timely and high-quality execution of all regulatory deliverables. **Your role:** + Serve as RA Representative on project teams,… more
    Philips (06/16/24)
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  • Associate Medical Director, Medical Affairs

    AbbVie (Waltham, MA)
    …and LinkedIn. Job Description Purpose: The Associate Medical Director provides specialist medical/scientific strategic and operational input into core medical ... affairs activities within their TA inclusive of healthcare professional/provider...Responsible for routine and adhoc safety monitoring reports to regulatory agencies. May review, assess and report applicable Adverse… more
    AbbVie (06/16/24)
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  • Director - Veterinary Insights and Medical…

    Merck (Boston, MA)
    …+ Have broad experience in Animal health commercial operations, R&D, and Regulatory Affairs + Expertise in project management, business adoption/change ... Consumer Affairs + Research and Development + Supply, Quality, Regulatory + Strategic Development and Innovation, Marketing, Sales, Salesforce Enablement and… more
    Merck (07/02/24)
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  • Regulatory Documentation Specialist

    Digital Prospectors (Boston, MA)
    regulatory complexities. + Collaborate with interdisciplinary teams, including regulatory affairs , quality assurance, research and development, and ... ** Regulatory Documentation Specialist ** **Boston, MA** **Job...relevant field such as life sciences, pharmacy, chemistry, or regulatory affairs . Advanced degrees or certifications may… more
    Digital Prospectors (05/29/24)
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  • Regulatory Specialist

    Beth Israel Lahey Health (Boston, MA)
    …just taking a job, you're making a difference in people's lives.** The Regulatory Specialist supports regulatory compliance for oncology clinical research ... required in Life Science or related field.. Master's degree preferred in Regulatory Affairs + 1-3 years related work experience required. + Must demonstrate good… more
    Beth Israel Lahey Health (04/06/24)
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  • Sr. Regulatory Specialist

    Beth Israel Lahey Health (Boston, MA)
    …Hours:** 32 **Work Shift:** Rotating (United States of America) The Sr. Regulatory Specialist supports regulatory compliance for clinical research ... degree in Life Science or related field required; Master's degree in Regulatory Affairs preferred. + Minimum of 3-5 years related work experience required. +… more
    Beth Israel Lahey Health (04/30/24)
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  • Risk & Patient Safety Specialist (RN…

    Beth Israel Lahey Health (Burlington, MA)
    …and facilitates regulatory investigations. The Risk Manager and Patient Safety Specialist plays an integral role in regulatory and accreditation readiness by ... lives.** **Job Description:** The Risk Manager and Patient Safety Specialist manages the review, investigation and reporting of safety events/incidents/occurrences… more
    Beth Israel Lahey Health (05/24/24)
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  • Risk Management & Patient Safety Specialist

    Beth Israel Lahey Health (Burlington, MA)
    …lives.** Position Summary: The Risk Manager and Patient Safety Specialist manages the review, investigation and reporting of safety events/incidents/occurrences ... safety and hospital liability in accordance with established hospital, regulatory , and accreditation procedures, guidelines and criteria. This individual will… more
    Beth Israel Lahey Health (06/07/24)
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  • L&D Specialist , Global QMS Training

    Olympus Corporation of the Americas (Westborough, MA)
    …Compliance Manager at 1-888-Olympus (###). Posting Notes: || United States (US) || Massachusetts (US-MA) || Westborough || Quality & Regulatory Affairs (QA/RA) ... than @Olympus.com, it is likely not legitimate. **Job Description** The training specialist will support the management of the global training process by… more
    Olympus Corporation of the Americas (06/29/24)
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  • Field Clinical Research Specialist

    Medtronic (Boston, MA)
    …from key functional groups (Research & Development, Manufacturing, Sales, Marketing, Regulatory Affairs , Legal, and European Clinical groups). + Identify ... tool in battling the global hypertension epidemic. The **Field Clinical Research Specialist ** is a field based, customer- facing position responsible for clinical… more
    Medtronic (07/04/24)
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  • Quality Systems Specialist Complaints

    Randstad US (North Billerica, MA)
    …Support, Engineering, Analytical Laboratories, Manufacturing, Validation, Customer Service and Regulatory Affairs groups to ensure timely complaint ... quality systems specialist complaints. + north billerica , massachusetts + posted 2 days ago **job details** summary + $50 - $58 per hour + contract + bachelor… more
    Randstad US (07/03/24)
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  • Principal Client Inquiry and Audit…

    Pegasystems (Boston, MA)
    Principal Client Inquiry and Audit Specialist Job Category: Information Technology Location: US - Massachusetts - Remote | US - Virginia - Dulles + ShareCopying ... compliance management, risk management, auditing, IT Security or similar regulatory programs + 3+ years Cloud Knowledge, IT /...compensation) under laws administered by the Secretary of Veterans Affairs ; or 2. a person who was discharged or… more
    Pegasystems (06/12/24)
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  • Senior Risk Manager

    Tufts Medicine (Boston, MA)
    …**Job Description** **Minimum Qualifications** **:** 1. Bachelor's degree in Law, Regulatory Affairs , Compliance, Nursing, Healthcare Administration or related ... risks to acceptable levels, internal and external stakeholder reporting, including regulatory reporting. A professional individual contributor role that may direct… more
    Tufts Medicine (07/03/24)
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  • Senior Housing Compliance Manager

    Pine Street Inn (Jamaica Plain, MA)
    …Education and Experience: Bachelor-s degree or equivalent is recommended. Certified Occupancy Specialist or similar designation required. At least 5 years of related ... Degree + Valid MA Driver-s License in good standing + Certified Occupancy Specialist (COS) + Low Income Housing Tax Credit designation PREFERRED: + Strong experience… more
    Pine Street Inn (06/03/24)
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  • Associate Engineering Fellow, Process Engineering

    Takeda Pharmaceuticals (Cambridge, MA)
    …chemistry, analytical development, drug product development, manufacturing, quality assurance, and regulatory affairs , to develop and implement effective process ... or business processes. + Responsible for authoring relevant sections of regulatory documents, validation plans, development reports, process flow diagrams (PFDs),… more
    Takeda Pharmaceuticals (05/03/24)
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