Technical Project Manager

Join a world-class manufacturer at the forefront of innovation in medical device engineering.

We are proud to be working with a true market leader in advanced products and systems for the health care and medical industries, with over 3,500 employees across multiple global sites. The UK operation, based in Lancashire, has recently received £12m investment in machinery, clean room facilities, and full site refurbishment.

With a strong commitment to sustainability, innovation, and engineering excellence, they are continuing to invest in their people, technologies, and facilities to remain a leader in the healthcare and life sciences sectors.

As Technical Project Manager, you will take ownership of multiple high-value manufacturing projects, some valued at over £8 million. Leading the full lifecycle from concept through to commercial launch. You will manage cross-functional teams, liaise with stakeholders across departments and international colleagues in Europe, and ensure all project goals are met from technical, strategic, and regulatory standpoints.

This is a pivotal leadership role in a regulated environment, ideal for someone from a medical device, healthcare manufacturing, or high-volume injection moulded product background.

• Lead large-scale medical product development and manufacturing projects
• Manage timelines, budgets, deliverables, and risk assessments
• Act as the primary point of contact for internal stakeholders and clients
• Oversee design reviews, V&V testing, risk management, and regulatory compliance
• Collaborate with cross-functional teams (R&D, Regulatory, Operations, Quality)
• Ensure smooth design transfer and integration into production & supply chain
• Provide status updates to senior leadership and European HQ
• Maintain accurate documentation and project records
• Occasionally travel to support international collaboration and project delivery

• Minimum 3 years’ experience in technical project management
• Strong technical/engineering background (degree in Engineering or Industrial Design)
• Proven ability to manage full product lifecycle in regulated environments
• Exceptional communication and stakeholder engagement skills
• Skilled in project planning, documentation, and issue resolution
• Experience in Healthcare, medical device manufacturing or regulated industries
• Understanding of injection moulding processes/tooling
• Familiarity with ISO
  9001 / ISO
  13485
• Competency in 3D modelling/CAD and engineering documentation

• Performance-related bonus
• Private medical insurance
• Hybrid working and flexible hours
• Opportunities to travel and collaborate internationally
• Newly refurbished, state-of-the-art manufacturing site

This is an exceptional opportunity to join a forward-thinking, globally respected manufacturer and play a critical role in bringing next-generation medical products to market.