Senior Process Engineering - Orthopaedics

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

At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.Learn more at jnj.com.

As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.

Job Function:

Supply Chain Engineering

Job Sub Function:

Process Engineering

Job Category:

Scientific/Technology

All Job Posting Locations:

Blackpool, Lancashire, United Kingdom

Job Description:

“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.”

Position Overview

The Senior 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.

Required Qualifications & Experience

• 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.

Key Competencies

• 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.

Required Skills:

• Continuous Improvement, Process Validation, Quality Validation

Preferred Skills:

• Analytical Reasoning, Computerized Equipment Skills, Emerging Technologies, Gemba Kaizen, Issue Escalation, Lean Supply Chain Management, Problem Solving, Process Control, Process Engineering, Process Oriented, Product Improvements, Science, Technology, Engineering, and Math (STEM) Application, Situational Awareness, Supply Planning, Technical Research, Technologically Savvy, Validation Testing

Required Skills:

Lean Manufacturing, Pharmaceutical Process Engineering

Preferred Skills:

Analytical Reasoning, Computerized Equipment Skills, Emerging Technologies, Gemba Kaizen, Issue Escalation, Lean Supply Chain Management, Problem Solving, Process Control, Process Engineering, Process Oriented, Product Improvements, Science, Technology, Engineering, and Math (STEM) Application, Situational Awareness, Supply Planning, Technical Research, Technologically Savvy, Validation Testing

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