QA Specialist: cGMP Compliance & Batch Release
TechDigital Group
A biopharmaceutical company in New Jersey is seeking a Quality Assurance Specialist to support cGMP quality operations. The role focuses on ensuring compliance with regulatory standards through the review of controlled documents, batch records, and deviations. Candidates should have a degree in science or engineering and 3-5 years of cGMP experience. Strong attention to detail and effective communication skills are essential. This position offers a blend of onsite and remote work. #J-18808-Ljbffr
Vacancy posted 6 hours ago
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