Regulatory Project Lead - FDA & Global Submissions
Puretek Corporation
Puretek Corporation is seeking a Regulatory Project Manager in Los Angeles, CA to serve as a cross-functional coordinator between operations and quality teams. You will drive timelines and ensure that regulatory deliverables are complete and compliant across multiple client projects. Ideal candidates hold a Bachelor’s degree in a related scientific field and have 1–4 years of experience in regulatory affairs. Join us to gain exposure to FDA and global regulatory requirements! #J-18808-Ljbffr Puretek Corporation
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