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Seeking a QA Inspector with experience in pharmaceutical manufacturing to ensure product quality throughout the production lifecycle. This role focuses on in-process checks sample collection and compliance with GMP standards.
Key Responsibilities:Perform in-process quality checks and testing (e.g. LOD bulk density weight variation).
Collect blend uniformity validation and finished product samples.
Dispense and verify materials; ensure line clearance.
Use ERP systems (SAP) for posting and tracking materials.
Support investigations into deviations OOS/OOT and non-conformances.
Conduct daily quality rounds and escalate issues.
Review batch records logs and calibration reports.
Ensure rejected materials are properly isolated and recorded.
High School Diploma with strong science exposure.
1 2 years of pharmaceutical experience (DPI MDI or Injectables only).
Strong knowledge of GMP and 21 CFR Part 820.
Good communication documentation and basic computer skills.
Full-time