Process Engineer, Medical Devices & Validation

Brighter Signals

Lancashire

In loco

GBP 45.000 - 65.000

Tempo pieno

3 giorni fa
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Descrizione del lavoro

Johnson & Johnson's Orthopaedics team in the UK seeks a Process Engineer to own and optimize manufacturing value streams for safe, compliant production of medical devices. Lead validation programs and drive continuous improvement initiatives across functions.

You will mentor junior engineers, participate in governance and regulatory discussions, and contribute to improving quality, supply continuity and cost performance while aligning with DePuy Synthes transition plans.

Competenze

  • Bachelor’s degree or equivalent in Engineering (Mechanical, Chemical or Automation).
  • 2 years manufacturing/process engineering experience.
  • Experience leading validation activities including IQ, OQ and PQ for equipment, processes and systems.
  • Experience managing Audit Actions, NCRs and CAPAs within a Quality Management System.
  • Strong experience in structured problem solving and root cause analysis.
  • Excellent technical content skills (specifications, validation protocols, change control).
  • Experience leading multi-functional teams.

Mansioni

  • Own and optimize assigned manufacturing value streams to ensure safe, compliant production of medical devices.
  • Lead complex process development and validation programs.
  • Drive multi-functional continuous improvement initiatives and cost performance.
  • Mentor junior engineers and represent Engineering in governance and regulatory forums.
  • Improve quality, supply continuity and cost performance across operations.

Conoscenze

Process Engineering
Continuous Improvement
Quality Validation
CAPA

Formazione

Bachelor’s degree in Engineering

Strumenti

Siemens
Rockwell
HMI
OT Architecture

Descrizione del lavoro

Johnson & Johnson's Orthopaedics team in the UK seeks a Process Engineer to own and optimize manufacturing value streams for safe, compliant production of medical devices. Lead validation programs and drive continuous improvement initiatives across functions.

You will mentor junior engineers, participate in governance and regulatory discussions, and contribute to improving quality, supply continuity and cost performance while aligning with DePuy Synthes transition plans.

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