Conduct analytical testing and ensure accurate documentation for: API / drug substance / drug product / finished product samples, complaint samples, stability samples, and packaging material samples
Handle sample storage and laboratory documentation in accordance with cGxP standards
Guarantee compliance with data integrity principles
Perform maintenance, calibration, and qualification of analytical equipment
Support stability activities, including testing and documentation (when not centralized)
Strictly adhere to HSE guidelines and proactively identify and report risks
Maintain a constant state of inspection readiness
Contribute to continuous improvement initiatives and process optimization
Complete mandatory training activities within the defined timelines
Work according to a defined shift rotation system to ensure operational continuity
ABOUT YOU
1 to 3 years of experience in a pharmaceutical laboratory environment (Quality Control, Quality Assurance, or Production preferred)
Experience with aseptic techniques is considered an advantage
Completed apprenticeship as a laboratory assistant or equivalent qualification
Strong teamwork skills and a results-driven mindset
Knowledge of GMP, GxP standards, TQM principles, and laboratory best practices
Familiarity with QC testing, sampling procedures, and laboratory equipment
Structured, rigorous, and able to work efficiently in a regulated environment
Analytical, resilient, and committed to operational excellence
