Latest Medical Device Regulatory Affairs jobs - JobisJob United States Mobile

188 Medical Device Regulatory Affairs Jobs

Director Regulatory Affairs Medical Device Shepherd Regulatory Search - Marlborough, MA, United States approvals to market devices throughout the product development lifecycle while building and managing a regulatory team. Responsibilities: Develop strategies for regulatory approval of medical devices 18 days ago
(Medical Device) Director, Quality and Regulatory Affairs Bright Uro - Irvine, CA, United States Uro markets, including Registration, Non-Conformities, Product Recalls, Field Actions and Medical Device Reporting. Maintain and update regulatory files and binders. Education and Work Experience 20 days ago
Manager, Regulatory Affairs - Medical Devices Allergan Aesthetics - Irvine, California Represents US Regulatory in project teams. Develops US regulatory filing strategy, with input from supervisor. Provides regulatory... 5 days ago
Regulatory Affairs Manager EPM Scientific - San Jose, CA, United States Title: Regulatory Affairs Manager Location: San Jose, CA Base Salary: $140,000-$190,000 About: Currently working with a medical device company dedicated to developing and commercializing breakthrough 2 days ago
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Senior Regulatory Affairs Associate Elucent Medical, Inc. - Eden Prairie, MN, United States 5 years of medical device Regulatory Affairs Proven track record with regulatory submissions. Experience preparing & defending regulatory submissions to the FDA (510(k) Knowledge of global regulatory 2 days ago
regulatory affairs expert-medical devices Randstad - st louis, missouri , we have the ideal position for you! The Regulatory Affairs Expert-Medical Devices manages assigned regulatory tasks related to health authority notifications, submissions, and registrations regarding renewals and new $30 - $33.10 per hour 13 days ago
Quality Regulatory Manager Gabriele & Company - Boston, MA, United States experience in Medical Device industry Regulatory Affairs knowledge Quality Management system knowledge 510K submissions Clinical submissions and trials MDR (Medical Device Rugulation/Reporting) ISO EU 4 days ago
Regulatory Affairs Specialist Kelly Science, Engineering, Technology & Telecom - Irvine, CA, United States Regulatory Affairs Specialist (hybrid) Kelly Science and Clinical FSP is currently seeking a medical device Regulatory Affairs Specialist II for a long-term engagement in Irvine, CA 6 days ago
Regulatory Affairs Specialist II (DePuy Synthes) - Medical Device Business Services, Inc. Johnson and Johnson - Raynham, MA Regulations and European Medical Device Regulations (and previous Medical Device Directives) Preferred : • Experience in orthopedics and orthopedic device regulatory requirements. • Experience 6 days ago
Regulatory Affairs Manager Catalyst Life Sciences - Chicago, IL, United States materials for accuracy, comprehensiveness, and compliance with regulatory standards. Experience Required 6 years' Regulatory Affairs experience within Medical Devices or IVDs, understanding FDA requirements 4 days ago

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