We're looking for a Senior Regulatory Affairs Specialist, working in the Biotechnology/Medical Devices industry in Northridge, California, United States.
Works with the regulatory affairs team, engineers, and technical experts to resolve potential regulatory issues and questions from regulatory agencies.
Prepares submissions and reports for the support other international agencies as required by product status.
Collaborate on submission activities for a variety of products to gain European device approvals.
We're offering Competitive Compensation and Benefits. This position may present an opportunity to go permanent.
Our client is an award-winning clinical development company. Improving lives globally with 20+ years’ experience in clinical research and strategic resourcing. Elevating results with proven strategies, comprehensive solutions, and customized delivery models.
Serving pharmaceutical, biopharmaceutical, biotechnology, and medical device organizations.
Strong relationships provide you connections and access to great opportunities. Industry expertise sets you up for success with helpful insights, career coaching, and professional training. Grow and learn while you put your skills to work.
Experience Required for Your Success
Bachelor's degree plus 3+ years of regulatory experience in the medical device, biotech, or pharmaceutical industry
EU Medical Device Regulation knowledge/application is highly preferred
What Do You Think?
Does your experience reflect what it takes to be successful in this role? Do the work and challenges get you excited about what's possible? Apply here.