Senior Process Engineer, Orthopedics Manufacturing

Johnson & Johnson Innovative Medicine

Lancashire

Presencial

GBP 65.000 - 90.000

Jornada completa

14 días+

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Descripción de la vacante

Johnson & Johnson Innovative Medicine in the United Kingdom is seeking a Senior Process Engineer to own and optimize manufacturing value streams for safe, compliant and cost‑effective production of medical devices. You will provide strategic technical leadership, lead complex validation programs and mentor junior engineers.

The role requires experience with IQ/OQ/PQ, CAPAs within a QMS, and a strong track record in structured problem solving and cross‑functional collaboration.

Formación

  • Bachelor’s degree or equivalent experience in Engineering (or equivalent).
  • Demonstrated ability in manufacturing/process engineering
  • Demonstrated experience leading validation activities including IQ, OQ and PQ for equipment, processes and systems.
  • Proven track record 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 and influencing collaborators at multiple levels.

Responsabilidades

  • Owns and optimizes manufacturing value streams for safe, compliant, and cost‑effective production.
  • Provide strategic technical leadership and lead validation programs.
  • Mentor junior engineers and drive continuous improvement initiatives.

Conocimientos

Continuous Improvement
Process Validation
Quality Validation
Lean Manufacturing
Pharmaceutical Process Engineering

Educación

Bachelor’s degree in Engineering

Descripción del empleo

Johnson & Johnson Innovative Medicine in the United Kingdom is seeking a Senior Process Engineer to own and optimize manufacturing value streams for safe, compliant and cost‑effective production of medical devices. You will provide strategic technical leadership, lead complex validation programs and mentor junior engineers.

The role requires experience with IQ/OQ/PQ, CAPAs within a QMS, and a strong track record in structured problem solving and cross‑functional collaboration.

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