Company Overview / Employee Value Proposition
STERIL Medical's products are used extensively in hospitals, clinics, nursing homes, dialysis centres and laboratories. We have been manufacturing disposable medical products in Singapore since 1988. We are dedicated to delivering products that will eventually simplify the work of doctors, nurses, and other healthcare providers in hospitals, medical practices, and nursing homes. With a commitment to excellence and a passion for innovation, we seek individuals who share our vision and drive for success.
Job Summary
Assist in daily production activities for medical devices, ensuring compliance with GMP and Quality System Regulations, supporting quality assurance processes, and maintaining cleanroom protocols to deliver safe and effective products.
Responsibilities
- Execute daily production schedules for medical devices and products to meet operational targets
- Monitor and document production processes to ensure compliance with GMP and Quality System Regulations
- Manage product records, History Records, and Bills of Materials (BOMs) to maintain accurate production data
- Support batch record review, product traceability, and lot control activities to uphold product quality and safety
- Coordinate with the Quality Assurance (QA) team to facilitate audits and implement corrective actions promptly
- Assist in managing cleanroom or controlled environment protocols to maintain required production conditions
- Track production key performance indicators (KPIs) such as yield, scrap, and efficiency within regulatory standards
- Enforce safety, hygiene, and gowning procedures on the production floor to ensure a safe working environment
- Facilitate clear communication between production, materials, and QC/QA teams to support smooth operations
Required competencies and certifications
- Minimum 2 years of experience in a production, operations, or technician role within an ISO-regulated environment (medical devices, disposables, pharmaceuticals)
- Working knowledge of GMP, ISO 13485, and FDA Quality System Regulations (QSR)
- Proven ability to follow and document Standard Operating Procedures (SOPs) with meticulous attention to detail
