Job Description
pPerform QA reviews of manufacturing, QC, and engineering records, and procedures to ensure compliance with cGxP regulatory requirements. Apply quality assurance systems, methods, and procedures to identify problems and generate alternatives and recommendations./pbrulbrliReview manufacturing, QC, and engineering documentation, including batch manufacturing records./librliAssist in customer complaint investigations and author Standard Operating Procedures (SOPs)./librliIdentify deviations from accepted practices, evaluate impact, and determine actions./librliReview and approve GMP Deviation investigations and CAPAs./librliPerform internal audits, walkthroughs, and participate in site projects./libr/ulbrpPreferred experience in pharmaceutical industry, knowledge of cGMPs, quality assurance systems, and OPEX Lean tools./pbrpTypical education: 4+ years relevant experience and a BS, or 2+ years and a MS./pbrpMorgan McKinley is acting as an Employment Agency./pbrpBy applying for this role, you agree to our Terms of Service and Privacy Statement./p