GMP Quality Systems Specialist: Document Control
$100k - $125kMapLight Therapeutics, Inc.
MapLight Therapeutics, Inc. seeks a Quality System Specialist to support the development of biotech products. This hybrid role requires strong knowledge of FDA regulations and experience in managing Quality Management Systems. The ideal candidate has a Bachelor’s in a scientific discipline and 5+ years in biotech. Responsibilities include managing controlled documents, supporting QA onboarding, and adhering to compliance standards. Compensation ranges from $100,000 to $125,000 with benefits including bonus opportunities and 401(K) matching. #J-18808-Ljbffr MapLight Therapeutics, Inc.
Vacancy posted 4 days ago
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