Process Engineer

The Process Engineer owns and optimizes assigned manufacturing value streams to ensure safe, compliant, and cost‑effective production of medical devices. In this role 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. You will mentor junior engineers, represent Engineering in governance and regulatory forums, and drive initiatives that improve quality, supply continuity, and cost performance.

Job Function: Supply Chain Engineering

Job Sub Function: Process Engineering

Job Category: Scientific/Technology

All Job Posting Locations: Blackpool, Lancashire, United Kingdom

Fueled by innovation at the intersection of biology and technology, we're developing the next generation of smarter, less invasive, more personalized treatments.

Are you passionate about improving and expanding the possibilities of Orthopaedics? Ready to join a team that's reimagining how we heal? Our Orthopaedics teams help keep more than 6 million people moving each year while delivering clinical and economic value to surgeons and healthcare systems. Our teams build solutions for joint reconstruction; trauma and craniomaxillofacial; sports, extremities, and elective foot and ankle; spine; and robotics and digital surgery.

Johnson & Johnson announced plans to separate our Orthopaedics business to establish a standalone orthopaedics company, operating as DePuy Synthes. The process of the planned separation is anticipated to be completed within 18 to 24 months, subject to legal requirements, including consultation with works councils and other employee representative bodies, as may be required, regulatory approvals and other customary conditions and approvals.

Should you accept this position, it is anticipated that, following conclusion of the transaction, you would be an employee of DePuy Synthes and your employment would be governed by DePuy Synthes employment processes, programs, policies, and benefit plans. In that case, details of any planned changes would be provided to you by DePuy Synthes at an appropriate time and subject to any necessary consultation processes.

Bachelor's degree or equivalent experience in Engineering (or equivalent) - Mechanical, Chemical or Automation

2 years 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.

Desirable experience on knowledge of control systems (Siemens/Rockwell), HMI's, OT Architecture and computer systems

Strategic and analytical problem solver with data‑driven decision‑making skills.

Structured problem solver with a focus on root cause and sustainable corrective actions.

Strong multi-functional collaborator and influencer (Operations, Quality, R&D, Suppliers); able to represent Operations in governance and regulatory settings.

Excellent written and verbal communication skills for technical content and collaborator updates.

Project organisation, prioritisation and execution with the ability to drive complex actions to timely closure.

Continuous improvement attitude with measurable focus on cost, quality and supply stability.

Commitment to Health, Safety and Environmental (HSE) practices and regulatory compliance

Continuous Improvement, Process Validation, Quality Validation