FSP - QC Reviewer

Job Description

• On-site QC Reviewer role in Foster City, CA, supporting pharmaceutical/biopharmaceutical analytical services.
• Reviews raw laboratory data, verifies numerical data for regulatory filings, evaluates compliance with analytical methods and SOPs, and documents deficiencies.
• Authors clinical and commercial stability protocols, transcribes and writes SOPs, consults on quality records, and consolidates QC metrics.
• Trains QC Reviewers and laboratory staff while communicating documentation issues and corrective actions to laboratory personnel and project leaders.
• Requires a Bachelor's degree in a relevant laboratory science plus 2+ years of experience, or a Master's degree; knowledge of GLP, GMP, chromatography, and Federal Regulations is required.