QA/RA Specialist — GLP/GMP, Audits & Regulatory Submissions
Synergy Bioscience company
Synergy Bioscience company is looking for a QA/RA Specialist in Dallas, Texas. The ideal candidate will have strong expertise in Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP) within the pharmaceutical industry, with at least 5 years of experience. Responsibilities include developing compliance documentation, conducting audits, and collaborating with teams to ensure adherence to FDA and EMA standards. Benefits include health care and paid time off. #J-18808-Ljbffr Synergy Bioscience company
Vacancy posted 3 days ago
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