Senior Regulatory Affairs Specialist (FDA experience mandatory)
- Provide Regulatory strategies for projects as RA representative in cross-functional teams
- Responsible for regulatory Assessment on product changes
- Coordinate the preparation of regulatory submissions (such as IDE, original PMA and supplements)in the context of new product and product changes in accordance with FDA requirements
- Coordinate the responses to questions raised by FDA
- Review of product labelling
- Participate in audits and inspections, ensuring compliance with FDA requirements
- Stay up-to-date with relevant regulations, guidelines, and industry trends, and provide strategic regulatory guidance to internal stakeholders
- Ensure accurate population of RA databases
- Maintain and update SOP's for Regulatory department
- Minimum 7 to 10 years of experience in Medical device or pharmaceuticals industry
- Proficient knowledge of quality standard (ISO 13485) and relevant regulations (21CFR part 820, MDR 2017 / 745) and appropriate laws, guidelines and industry standards Demonstrated experience in communicating with regulatory agencies including FDA and UE regulatory agencies
- Demonstrated experience in leading, writing and submission of complex regulatory filling(e.g. IDE, PMA, CE mark, etc )
- Demonstrated ability in analytical reasoning and critical thinking skills
- Good knowledge of relevant regulations (FDA)
- Ability to work on several projects simultaneously, ability to prioritize
- Fluent in English with at least a B2 level in French
Senior Regulatory Affairs Specialist (FDA experience mandatory)
Ensuring compliance with FDA requirementsStay up to date with relevant regulations, guidelines, and.. guidelines and industry standards Demonstrated experience in communicating with regulatory agencies..
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