Staff Supplier Quality Engineer

Johnson & Johnson

Blackpool, Lancashire, United Kingdom
Base: $94,000.00 - $151,800.00; bonus/equity: not ...
Supplier quality assurance leadership
Supplier qualification and process maintenance
Root cause analysis and corrective actions
The Staff Supplier Quality Engineer provides overall quality assurance leadership in the management of select contract manufacturing sites and raw material suppliers engaged in the production of Johnson and Johnson products

Job Summary

  • The Staff Supplier Quality Engineer provides overall quality assurance leadership in the management of select contract manufacturing sites and raw material suppliers engaged in the production of Johnson and Johnson products.
  • This role leads activities associated with resolving complex technical issues, supplier risk management, and supplier process improvement, requiring independent decision-making on technical problems and methods.
  • Employees are eligible for participation in the Company’s consolidated retirement plan, savings plan, and long-term incentive program, along with various time off benefits including vacation, sick time, holidays, and parental leave.

Matching Summary

The Staff Supplier Quality Engineer provides overall quality assurance leadership in the management of select contract manufacturing sites and raw material suppliers engaged in the production of Johnson and Johnson products.

Salary

Base: $94,000.00 - $151,800.00; Bonus/Equity: Not specified; Benefits: Not specified

Skills & Requirements

Must-have

  • Supplier quality assurance leadership
  • Supplier qualification and process maintenance
  • Root cause analysis and corrective actions
  • Supplier risk management
  • Process improvement initiatives
  • FDA CFR Part 820 and ISO 13485
  • Quality Systems support

Nice-to-have

  • Teamwork and problem-solving skills
  • Independent decision-making
  • Technical leadership
  • Project management
  • Communication and alignment
  • Stressful/fast-paced environment adaptability

Key Requirements

  • Bachelor's Degree required
  • 4-6 years GMP/ISO regulated industry experience
  • Medical device/pharmaceutical industry experience preferred
  • Engineering or science field of study preferred
  • FDA CFR and ISO regulations knowledge required
  • Six Sigma, Lean, ASQ certification preferred

Work Rights

Not specified

Tailored Resume

Cover Letter