19 Medical Device Regulatory Affairs Jobs in Andover, MA - page 2
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Senior Product Manager Aquent - Chelmsford, MA, United States lifecycle of our Advanced Life Saving Devices, from ideation to launch and beyond. This role requires a deep understanding of the medical device industry, clinical needs, and market trends. The Senior Product 14 days ago
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Principal Packaging Engineer Johnson & Johnson - Danvers, MA for medical devices, considering factors such as product protection, sterility, usability, and regulatory requirements. Collaborate with cross-functional teams, including R&D, Quality, Regulatory Affairs 25 days ago
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Director, US Regulatory Affairs, Ad/Promo & Labeling Proclinical Staffing - Cambridge, MA, United States schedule. Skills & Requirements: At least five (5) years of experience involving the direct implementation of promotional labeling and advertising regulations in the biotech/pharmaceutical/medical device 30 days ago
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Head of Device Development Biogen - Cambridge, Massachusetts of experts from regulatory sciences, pre-clinical, safety, clinical development, clinical operations, medical affairs and clin pharm. This team is accountable for the successful integration of the platform 22 days ago
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Sr Human Factors Engineer, R&D Collins Consulting Inc - Burlington, Massachusetts , biomechanics, human behavior, and physiology. Demonstrated ability to effectively integrate information from to varied disciplines including Engineering, Marketing, Clinical Affairs, and Regulatory Affairs 21 days ago
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Principal Regulatory Affairs Specialist Boston Scientific - Marlborough, MA, US Qualifications: Minimum of a Bachelor’s degree with a minimum of 5 years’ experience in Regulatory Affairs or a related discipline (e.g. Quality Systems, R&D, Quality, Post Market) within the medical device, IVD 22 days ago
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Senior Engineer, Device Design and Development Biogen - Cambridge, Massachusetts Factors, Packaging, Manufacturing Science, Project Management, Quality and Regulatory Affairs etc. The position will lead the design and process development of medical devices and combination product 21 days ago
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Michael Page- Boston- Program Manager- Product Development Michael Page - Lawrence, MA performance and compliance. Collaborate with internal teams, including R&D, engineering, manufacturing, regulatory affairs, and marketing, to drive program success. Foster a collaborative environment conducive $160,000 - $185,000/Year 3 days ago
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Regulatory Affairs Director ProClinical - Boston, MA operational excellence initiatives within the Regulatory Affairs department. If you are having difficulty in applying or if you have any questions, please contact Nicholas Walker at (+1) 646-367-2908 9 days ago
Top locations
- Cambridge, MA (4)
- Boston, MA (4)
- Raynham, MA (3)
- Burlington, MA (2)
- Marlborough, MA (2)
- Danvers, MA (1)
- Lawrence, MA (1)
- Chelmsford, MA (1)
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