Qa Ops Platform Lead

Johnson & Johnson UK

Yokneam, Haifa District, Israel
**
Supplier selection and qualification
Process validation and verification
Nonconformance & capa investigations
** Johnson & Johnson UK is seeking a QA Operation Platform Lead in Yokneam, Israel, responsible for quality management across product families, starting from supplier qualification to production processes. The ideal candidate will have experience in quality assurance within the medical device industry and will play a key role in supporting production quality and process improvements. **

Job Summary

  • The QA Operation Platform Lead is responsible for end-to-end quality management per product families, starting from Supplier selection and qualification, transfer to production processes and maintain supplier and process control during product lifecycle.
  • Key responsibilities include managing process validation/verification, supporting change control, leading improvement plans with suppliers, and contributing to operations production stabilization.
  • The role requires a BSc or qualification in Quality Assurance, practical knowledge of ISO13485, and experience with medical device electromechanics manufacturing.

Matching Summary

Match Score: 75

** Johnson & Johnson UK is seeking a QA Operation Platform Lead in Yokneam, Israel, responsible for quality management across product families, starting from supplier qualification to production processes. The ideal candidate will have experience in quality assurance within the medical device industry and will play a key role in supporting production quality and process improvements. **

Skills & Requirements

Must-have

  • Supplier selection and qualification
  • Process validation and verification
  • Nonconformance & CAPA investigations
  • Production stabilization and improvement

Nice-to-have

  • Business alignment and behavior
  • Human-centered design principles
  • Coaching and mentoring skills

Key Requirements

  • BSc or Qualification in Quality Assurance (CQE, CQM or CQA)
  • Practical knowledge of ISO13485
  • Experience with medical device electromechanics manufacturing
  • Ability to lead multidisciplinary projects

Work Rights

Not specified

Tailored Resume

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