Company Location: Bay Area Comp: 150K-220K Position Reports to: VP of Regulatory and Quality Director of Regulatory Affairs - San Francisco We are seeking a highly motivated and experienced Senior Director of Regulatory Affairs for a Medical Device Orthopedic Portfolio. This person will lead interactions with regulatory agencies globally and help develop & execute regulatory strategy. The person in this role manages a team over RA and QMS. Responsibilities Represent the regulatory function on manufacturing and product development teams to provide input on regulatory requirements, review and approve protocols, reports, and other product development and manufacturing documentation to ensure compliance with regulatory requirements. Manage the EUMDR transition to ensure continued business with existing products and timely new product CE marking. Work closely with research and development, clinical, quality, and marketing teams to ensure regulatory considerations are integrated into product development and launch plans. Develop and plan strategies and contingency plans for projects related to NPD. Provide direction and guidance to project teams to execute complex regulatory affairs projects & initiatives. Prepare documentation packages for submission to regulatory agencies globally. Interact with regulatory agencies as part of submission review and on-site audit support. Oversee team members in RA and QMS to execute business plans and strategies for RA success. Qualifications Education/Experience Requirements Bachelor’s degree required with a concentration in life sciences, technical, engineering, or related field Advanced degree strongly preferred 10+ years of experience in Regulatory Affairs submissions in a Senior/Principal/Program leadership function. 3+ years in a management capacity 3+ years of experience in medical device, drugs, biologics, and/or combination products preferred #J-18808-Ljbffr Biolink360
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