QA Specialist II - GMP Compliance (On-Site, San Diego)
$85k - $89kCatalent Pharma Solutions
Catalent Pharma Solutions is looking for a Quality Assurance Specialist II in San Diego. This role supports clinical trial projects with essential quality assurance processes throughout the product lifecycle. Responsibilities include batch record review, document authoring, and ensuring compliance with GMP standards. Applicants should have a high school diploma or GED, with further education preferred, alongside relevant GMP experience. The position offers a salary range of $85,000 to $89,000 annually, determined by experience and education. #J-18808-Ljbffr Catalent Pharma Solutions
Vacancy posted 3 days ago
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