Senior Process Engineer - Orthopedics

Johnson & Johnson MedTech

Blackpool, Lancashire, United Kingdom
Onsite
Manufacturing/process engineering
Validation activities including iq oq pq
Quality management system experience
Johnson & Johnson MedTech is seeking a Senior Process Engineer specializing in Orthopedics to optimize manufacturing processes for medical devices. The ideal candidate will possess strong engineering skills, particularly in process validation and problem-solving, while contributing to a culture of innovation and continuous improvement

Job Summary

  • The Senior Process Engineer owns and optimizes assigned manufacturing value streams to ensure safe, compliant, and cost‑effective production of medical devices.
  • You will provide strategic technical leadership, direct complex process development and validation programs, lead multi-functional continuous improvement initiatives, and influence long‑term process and equipment strategy.
  • Johnson & Johnson is committed to an inclusive work environment respecting diversity and dignity of employees and is undergoing a planned separation of its Orthopaedics business to establish DePuy Synthes.

Matching Summary

Match Score: 85

Johnson & Johnson MedTech is seeking a Senior Process Engineer specializing in Orthopedics to optimize manufacturing processes for medical devices. The ideal candidate will possess strong engineering skills, particularly in process validation and problem-solving, while contributing to a culture of innovation and continuous improvement.

Skills & Requirements

Must-have

  • manufacturing/process engineering
  • validation activities including IQ OQ PQ
  • quality management system experience
  • structured problem solving
  • multi-functional team leadership
  • technical content skills

Nice-to-have

  • analytical reasoning
  • computerized equipment skills
  • emerging technologies knowledge
  • Gemba Kaizen
  • lean supply chain management
  • situational awareness
  • technologically savvy

Key Requirements

  • Bachelor’s degree or equivalent experience in Engineering
  • experience leading validation activities IQ OQ PQ
  • experience managing Audit Actions NCRs CAPAs
  • strong root cause analysis skills
  • experience in Quality Management System
  • ability to influence collaborators at multiple levels

Work Rights

Not specified

Tailored Resume

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