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Job Description
QA specialist required for a 12 month contract. Performs QA reviews of manufacturing, QC and engineering records. Requires 4+ years of GMP experience, BS, and oral solid dose expertise. Key responsibilities:
- QA review of manufacturing, QC and engineering records
- QA review and approval of procedures and GMP deviations
- Demonstrates working knowledge of quality assurance systems and methods
- Demonstrates audit and investigation skills, and report writing skills
- Good verbal, written, and interpersonal communication skills
- 4+ years of GMP experience
- Oral solid dose pharmaceutical industry expertise
- Working knowledge of current Good Manufacturing Practices (cGMPs)
- Proficiency in Microsoft Office applications