QC Supervisor (Medical devices/Pharma)

Job Detail

Dream Job Alert! Become a QC Supervisor (Medical devices/Pharma, ID19668) at a foreign-invested company and earn $1200/month:

Manage, coach, and supervise Quality Control inspectors and technicians to ensure effective QC operations.
Plan, assign, and manage daily inspection and testing activities for incoming materials, in-process production, and finished products.
Ensure all inspections and tests are conducted in accordance with approved procedures, work instructions, and sampling plans.
Monitor QC laboratories and inspection areas, ensuring proper calibration, maintenance, and availability of inspection and testing equipment.
Ensure all QC activities comply with ISO 13485, GMP requirements, and internal Standard Operating Procedures (SOPs).
Participate in and support internal and external audits, including ISO 13485, GMP, notified body, and customer audits.
Lead investigations of non-conforming materials and products, including initiation of Non-Conformance Reports (NCRs).
Conduct root cause analysis and contribute to the development and implementation of corrective and preventive actions (CAPA).
Identify gaps and improvement opportunities within QC processes to enhance efficiency, compliance, and product quality.
Support the implementation of statistical tools and techniques for process monitoring and control.
Provide quality input for supplier qualification and supplier-related quality issues.
Support new product development and transfer activities.
Perform other duties as assigned by Superior

Male, under 45 years old.
Bachelor’s degree in Science, Engineering, or Pharmacy.
3–5 years of experience as a QC Supervisor in the medical device or pharmaceutical manufacturing industry.
Strong knowledge and hands-on experience in ISO 13485, GMP, and risk management.
Proficient in English.
Direct experience working with customers and using measurement instruments, inspection techniques, and quality testing equipment to ensure products meet required standards.