Job Description

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

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.

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