Pioneering trusted medical solutions to improve the lives we touch: Convatec is a global medical products and technologies company, focused on solutions for the management of chronic conditions, with leading positions in advanced wound care, ostomy care, continence care, and infusion care. With around 10,000 colleagues, we provide our products and services in almost 100 countries, united by a promise to be forever caring. Our solutions provide a range of benefits, from infection prevention and protection of at-risk skin, to improved patient outcomes and reduced care costs. Convatec’s revenues in 2023 were over $2 billion. The company is a constituent of the FTSE 100 Index (LSE:CTEC). To learn more about Convatec, please visit http://www.convatecgroup.com
We devise, develop and manufacture innovative products and services that support people with deeply personal and challenging medical conditions, helping to improve care for them and giving them greater confidence, freedom and mobility.
We are guided by our five core values, that shape the way we work, every day: Improve Care, Deliver Results, Grow Together, Own It and Do What’s Right.
At Convatec, we’re transforming our business for the better. Better products. Better ways of working. And better ways of delivering for our customers and each other. We’re aiming for nothing short of excellence. Join us on our journey to #ForeverCaring as a Project Engineer and you’ll do the same.

JOB SUMMARY

We are seeking a hands-on and proactive Project Engineer to join our Global Engineering team at our Deeside Advanced Wound Care facility. This is a key role supporting the introduction and integration of new automated manufacturing equipment. You will act as the engineering lead on existing projects, collaborating closely with the Project Manager and Validation Engineer to ensure delivery of equipment that fully meets the required safety standards, URS requirements, and all relevant regulatory standards.

DESIRABLE AND QUALIFICATIONS

• Degree or equivalent in an Engineering discipline.
• Experience in equipment process validation and capability studies
• Medical device manufacturing experience.
• Process FMEA, quality control methodologies.
• Involvement in capital equipment specification and vendor selection.
• Trackwise experience
• Apprenticeship-trained engineers or candidates with strong manufacturing-based qualifications will be prioritised.
• Other regulated or high-volume manufacturing environments will be considered.

TRAVEL REQUIREMENTS

• Yes, up to 20%

DUTIES AND RESPONSIBILITIES

• Act as engineering lead for projects introducing new manufacturing equipment and modification of existing process.
• Own and drive equipment delivery from initial specification through design reviews, FAT/SAT, and full validation (IQ/OQ/PQ).
• Coordinate with vendors to ensure designs meet technical and regulatory requirements.
• Lead technical investigations and process improvements during equipment development and integration.
• Support production handover and help drive consistent output, quality, and performance.
• Update and maintain documentation in compliance with GMP, change control, and internal standards.
• Identify and implement opportunities for cost reduction (COGs), uptime improvement, and lean manufacturing.
• Ensure engineering activities adhere to site and corporate EHS policies and procedures.
• Seek continuous improvement (CI) opportunities throughout project phases.
• Adhere to legal, corporate and site legislation and procedures