SUMMARY
Our client, a leader in ophthalmic pharmaceutical compounding, is expanding our Quality team! We currently have multiple openings within Quality Assurance (QA) and Quality Control (QC) . Applicants may be considered for several roles depending on background and interest, including :
- QC Sampling & Stability Coordinator
- QA Inspector
- QA Manufacturing Specialist
- QA Specialist – Complaints
- QA Specialist – Validation Document Reviewer (short-term)
RESPONSIBILITIES (vary by role) :
Support QC sample handling, stability studies, and documentation.Perform QA inspections of drug products, materials, and documentation.Oversee manufacturing quality processes, deviations, and CAPAs.Investigate product complaints and ensure timely closure.Review validation and calibration records for compliance.QUALIFICATIONS
Prior GMP / cGMP experience in pharma, biotech, or related industry.Strong documentation, QA / QC, and compliance background.Ability to work in an aseptic / cleanroom environment (gowning required).Excellent attention to detail and communication skills.WHY JOIN?
Growing company with career advancement opportunities.Stable environment with strong leadership support.Collaborative team culture in a compliant 503B facility.