Senior Process Engineer, Orthopedics Manufacturing

Johnson & Johnson Innovative Medicine; Lancashire; On-site; GBP 65,000 - 90,000; Full time

Job summary

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.

Qualifications

• 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.

Responsibilities

• 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.

Skills

Continuous Improvement

Process Validation

Quality Validation

Lean Manufacturing

Pharmaceutical Process Engineering

Education

Bachelor’s degree in Engineering

Job description

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.