• Sr. Regulatory Affairs

    Medtronic (Mansfield, MA)
    …in a more connected, compassionate world. **A Day in the Life** The Senior Regulatory Affairs Specialist (Sr. RAS) is responsible for collaborating, planning ... development and review process + Provide business and product information to the international regulatory affairs team to enable development and strategies… more
    Medtronic (07/01/25)
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  • Sr. Regulatory Affairs

    ConvaTec (Lexington, MA)
    …**Dimensions:** **Team** Part of a small team. Reporting to Senior Manager - International Regulatory Affairs , additional direction from Sr. Director, ... The primary responsibilities of the position are to drive improvements in regulatory affairs processes, systems and infrastructure whilst supporting … more
    ConvaTec (08/02/25)
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  • Principal Regulatory Affairs

    Philips (Cambridge, MA)
    …member of the Philips Ultrasound- Regulatory Affairs Organization, the Principal Regulatory Affairs Specialist will lead and provide regulatory ... visits by Notified Body. May represent Philips in an international committee chartered to develop an applicable standard. **You're...if:** + You have a minimum of 8+ years' Regulatory Affairs experience within FDA regulated Medical… more
    Philips (06/28/25)
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  • Principal Reg Affairs Specialist

    Medtronic (Boston, MA)
    …in a more connected, compassionate world. **A Day in the Life** Job Summary: Principal Regulatory Affairs Specialist As a Principal Regulatory Affairs ... and approvals for international market access, ensuring alignment with international regulatory requirements (RF, non-medical and medical). In collaboration… more
    Medtronic (07/30/25)
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  • Medical Records Technician (Coder In/Out Patient)

    Veterans Affairs, Veterans Health Administration (Leeds, MA)
    …and procedure. To perform this task, they must possess expertise in International Classification of Diseases (ICD), Current Procedural Terminology (CPT), and the ... services. Selects and assigns codes from the current versions of the International Classification of Diseases (ICD) Clinical Modification (CM) and Procedure Coding… more
    Veterans Affairs, Veterans Health Administration (07/31/25)
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  • Sr. QA Specialist , Operations

    Catalent Pharma Solutions (Chelsea, MA)
    …of final products. **EDUCATION AND** **EXPERIENCE** : Requires a Bachelor's degree in Drug Regulatory Affairs and 4 years of experience in job offered or 4 ... **Job Title:** Sr. QA Specialist , Operations **City:** Chelsea **State** : MA **JOB...various quality assurance checks during all manufacturing processes; Assess regulatory and quality risks in manufacturing activities and processes… more
    Catalent Pharma Solutions (07/24/25)
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  • Head of Global Scientific Communications…

    Takeda Pharmaceuticals (Cambridge, MA)
    …of regulatory guidelines and compliance requirements relevant to medical affairs activities. + Proven leadership and people management skills and the ability ... excellence and support the medical strategy teams by providing specialist knowledge and capabilities to support the disease areas...and advance digital innovation and data analytics in medical affairs . Under the direction of this role, the teams… more
    Takeda Pharmaceuticals (07/15/25)
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