About the role
AI summarisedThe QC Analyst III is responsible for managing sample storage, performing analytical testing, and ensuring documentation complies with cGxP standards. The role also supports HSE compliance, participates in training, and works a 12‑hour rotating shift in a pharmaceutical laboratory environment.
BiopharmaOnsiteQuality | Operations
Key Responsibilities
- Analytical testing and documentation of API / drug substance / drug product / finished product / Complaints / stability / packaging material samples
- Ensure all activities in compliance with cGxP, incl. data integrity
- Stability (when not centralized) testing/sample storage and management analytical documentation of stability samples to cGxP standards
Requirements
- Testing/Sample storage and management
- Comply with all HSE guidelines
- Preferred: Previous experience working in a laboratory environment in the pharmaceutical industry (quality assurance, production), aseptic technique.
- Collaboration; result-oriented