Perform analytical testing of incoming raw material samples using compendial methods (FTIR, wet chemistry identity testing, etc.).
Manage sample receipt, storage and reagent preparation according to cGxP requirements.
Conduct raw material method validation/verification and routine release testing.
Document analytical activities in compliance with GMP, HSE and data integrity standards.
Support stability testing and associated sample management when applicable.
Participate in laboratory investigations (OOS, deviations) and support related change controls.
Maintain QC Raw Materials laboratory in full cGMP compliance and support audits/inspections.
Contribute to continuous improvement projects within the QC laboratory.
ABOUT YOU
Academic background: Degree in Chemistry, Biochemistry, Pharmaceutical Sciences or equivalent scientific field, or completed apprenticeship as a laboratory technician.
3 to 5 years of experience in pharmaceutical laboratory environments (quality control, quality assurance or production).
Experience with analytical testing of raw materials (FTIR, wet chemistry identity tests, reagent preparation).
Knowledge of GMP and cGxP compliance requirements.
Experience with data entry, review and preparation of QC release packages.
Academic background: completed apprenticeship as laboratory assistant or equivalent training.
You are collaborative, result-oriented and demonstrate strong problem-solving and organizational skills.
