Responsibilities
- Execute the assembly, calibration, and testing of medical devices in strict accordance with ISO 13485 standards.
- Lead weekly and monthly physical stock takes for raw materials and finished goods to ensure inventory accuracy. Reconcile physical inventory counts with digital records and resolve any discrepancies immediately.
- Track and report scrap or rejected components to support lean manufacturing and cost-efficiency goals.
- Maintain controlled environments by following strict cleanroom sterilization and contamination control procedures.
- Monitor reorder levels for critical components and coordinate with procurement to prevent production downtime.
- Manage device traceability by assigning and tracking batch/lot numbers from raw materials to final dispatch. Ensure all inventory handling aligns with medical-grade quality and safety protocols.
Requirements
- Diploma in Biomedical Engineering, Pharmaceutical Technology, or Supply Chain Management with a technical background.
- Minimum 2 years of experience in a medical device or high- precision manufacturing environment.
- Deep understanding of ISO 13485 (Medical Devices - Quality Management Systems) and proficiency in inventory software (ERP/SAP).
- Exceptional numerical accuracy and mathematical skills for precise stock reconciliation and unit measurements.
- Ability to manage high-volume SKUs (Stock Keeping Units) with a methodical approach to labeling and storage.
- High level of ethics and a "zero-error" mindset regarding life- saving equipment.
- Strong communication skills to effectively coordinate between production staff and warehouse managers.
- Advanced proficiency in Excel and digital inventory tracking tools.
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