Perform QC inspections on raw materials, in-process, and finished IVD products
Ensure production activities comply with established quality standards and SOPs
Manage and monitor warehouse conditions (e.g., storage, temperature control, FIFO/FEFO)
Oversee inventory accuracy, stock control, and traceability of materials and products
Handle non-conformance, deviations, and support CAPA implementation
Maintain QC records and documentation in compliance with QMS (e.g., ISO 13485)
Support internal/external audits and regulatory inspections
Collaborate with production, supply chain, and QA teams to drive continuous improvement

Diploma/Degree in Life Sciences, Biomedical, Chemistry, or related field
At least 2 years of experience in QC within medical devices / IVD / pharmaceutical industry
Familiar with ISO 13485, GMP, and regulatory requirements
Knowledge of QC processes, warehouse management, and inventory control
Strong attention to detail and documentation skills
Able to work in a fast-paced, regulated environment