GMP Auditor, Med Device (Ex-FDA Preferred)
ProPharma(19 days ago)
About this role
ProPharma is seeking a compliance auditor to conduct onsite assessments in San Diego, focusing on regulatory and quality management systems in the biotech, med device, and pharmaceutical industries. The role involves evaluating facilities, documentation, and personnel against industry standards and regulations.
Required Skills
- Regulatory Compliance
- Auditing
- GMP
- EMA
- FDA
About ProPharma
propharmagroup.comProPharma helps navigate the complexities of drug development and ensure patient health and safety throughout the product lifecycle.
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