Latest Medical Device Regulatory Affairs jobs (page 3)

176 Medical Device Regulatory Affairs Jobs - page 3

Planning Analyst Insight Global - Irvine, CA, United States . This person will be responsible for working with regulatory affairs, Research & Development, Supply Chain, and Quality to support franchise projects concerning one medical device unit, planning integration, etc 3 days ago
Director, Regulatory Affairs, Ad/Promo & Labeling Proclinical Staffing - Raleigh, NC, United States /medical device industry. Extensive experience providing regulatory input and evaluation as part of a promotional review committee. The Associate Director, US Regulatory Affairs, Advertising & Promotion 3 days ago
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 3 days ago
Senior Regulatory Affairs Specialist DemeTECH Corporation - Miami Lakes, FL, United States with experience supporting compliance. Experience: 6-8 years of experience in Regulatory Affairs, including preparation of submissions to the FDA/EU. A minimum of 6 years of experience in medical device, drugs 3 days ago
EMC Test Engineer EPM Scientific - , NY, United States devices. Role and Responsibilities: As an EMC Test Engineer, you will play a vital role in ensuring our medical devices meet electromagnetic compatibility (EMC) standards. Here are the key responsibilities 8 days ago
Principal Regulatory Affairs Specialist MicroVention-Terumo - Aliso Viejo, CA, United States , responsible for submission activities focused on US/EU/Canada and for ensuring compliance to FDA and international regulatory agency requirements for Neurovascular and Peripheral medical devices. What You'll 3 days ago
Principal Regulatory Specialist Amplitude Vascular Systems - Boston, MA, United States related experience in medical device industry. Regulatory Affairs Certification expected (US) Experience with design controls, including mechanical, software/firmware and risk management review. Experience 22 days ago
Senior Regulatory Affairs Specialist Laborie - Portsmouth, NH, United States relevant discipline Minimum 5-8 years’ experience in Regulatory Affairs in the medical device industry FDA, EU, Health Canada, and international registrations experience Working knowledge with quality system 11 days ago
Site Quality Manager Kerry Search Partners - , CA, United States . TrackWise, AGILE, E1/SAP, LIMS or similar Competency of bioprocessing technology and capabilities, pharmaceutical production, pharmaceutical new product or medical device introductions Knowledge of project 5 days ago
Regulatory Affairs Specialist GForce Life Sciences - Lake Forest, IL, United States combination of education and experience. 4+ years’ experience in Regulatory Affairs role. Strong knowledge of IVDR and EU regulatory requirements is required. 1+ years’ experience in an IVD or medical device 11 days ago

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