Job Description
* Perform QC checks on raw materials, in-process, and finished IVD products
* Ensure compliance with quality standards and SOPs
* Plan and monitor production schedules to meet timelines
* Coordinate with teams to ensure materials and resources are ready
* Manage warehouse conditions and inventory (FIFO/FEFO, traceability)
* Handle non‑conformance and support CAPA actions
* Maintain QC documentation in line with ISO 13485
* Support audits and inspections
* Work with cross‑functional teams to improve processes
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
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