Qc Supervisor

Danaher UK

Not specified
Raw material inspection procedures
Production quality control management
Finished product release processes
Danaher UK is seeking a QC Supervisor responsible for overseeing quality control processes in medical manufacturing, including inspection, nonconformance handling, and laboratory management. The ideal candidate should have over 8 years of experience in quality roles, familiarity with GMP and ISO 13485 regulations, and strong communication skills

Job Summary

  • The role is responsible for establishing and managing quality control procedures across raw materials, production, and finished products.
  • Candidates must possess over 8 years of quality experience in medical manufacturing enterprises with a focus on GMP and ISO 13485 regulations.
  • The position involves leading laboratory management, nonconformance handling, and conducting internal and external audits to ensure regulatory compliance.

Matching Summary

Match Score: 85

Danaher UK is seeking a QC Supervisor responsible for overseeing quality control processes in medical manufacturing, including inspection, nonconformance handling, and laboratory management. The ideal candidate should have over 8 years of experience in quality roles, familiarity with GMP and ISO 13485 regulations, and strong communication skills.

Skills & Requirements

Must-have

  • Raw material inspection procedures
  • Production quality control management
  • Finished product release processes
  • Nonconformance handling and risk assessment
  • Laboratory equipment validation
  • GMP and ISO 13485 regulatory compliance
  • CAPA management and root cause analysis

Nice-to-have

  • Strong communication and teamwork skills
  • Good English speaking and writing skills
  • Experience in foreign-invested medical device manufacturing
  • Project development phase quality management
  • Environmental monitoring in clean areas

Key Requirements

  • Bachelor's degree in science or engineering
  • Over 8 years of quality experience in medical manufacturing
  • ISO 13485 internal auditor certification
  • Familiarity with GMP and ISO 13485 regulations
  • Over 5 years of production quality control management experience

Work Rights

Not specified

Tailored Resume

Cover Letter