Job Summary

This will be an 8-month contract role with 12-hour rotational shifts. You will perform quality control laboratory tasks following cGxP regulations, including sample management, analytical testing, and equipment maintenance to ensure product quality and compliance.

Responsibilities

Operational

• Store and manage samples accurately to maintain traceability and integrity
• Perform analytical testing on API, drug substances, drug products, finished products, complaints, stability, and packaging material samples to verify quality standards
• Document analytical test results clearly and accurately to support compliance and traceability
• Ensure all laboratory activities comply with cGxP regulations, including maintaining data integrity
• Conduct stability testing and manage stability sample storage according to cGxP standards when stability testing is not centralized
• Maintain, calibrate, and qualify analytical equipment to ensure reliable and accurate laboratory results

HSE

• Comply with all HSE guidelines
• Detect and report potential accidents, risks and propose solutions
• Responsible for participating in initial training and retraining

Requirements

• Previous experience working in a laboratory environment in the pharmaceutical industry (quality assurance, production), aseptic technique.
• Completed apprenticeship as a laboratory assistant or equivalent training