Job Description

• 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
  

Job Requirements

• 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