Medical Device Development Specialist

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic, and labelling is accurate.

Eurofins is dedicated to delivering testing services that contribute to the health and safety of society and the planet, and to its corporate responsibility to protect the environment and ensure diversity, equity, and inclusion across the entire network of Eurofins companies.

Eurofins PSS Insourcing Solutions® is a global, award-winning in sourcing solution. We place our skilled team directly at the client site, managing operations seamlessly and eliminating complexities. We ensure a strategic, long-term service commitment that delivers value directly at the client’ site, utilising their facilities, equipment, and methodologies, while maintaining the same service, expertise, and cGMP compliance available at the Eurofins facility.

If you're an employee seeking an exceptional career journey, Eurofins PSS Insourcing Solutions® is your gateway to a future where innovation, collaboration, and success converge. Join us in a world where excellence knows no boundaries!

We’re proud to be an armed forces-friendly place to work and welcome applications from reservists, armed forces veterans (including the wounded, injured and sick), as well as cadet instructors, and military spouses and partners.

Unfortunately, we are unable to offer visa sponsorship for this role.

This is a full time, permanent position, working a flexible 37 hour week, Monday – Friday.

As a Device Development Lead, you will be responsible for supporting cross-functional project teams in the development, industrialisation, verification and validation of drug delivery devices. You will work closely with internal scientific, manufacturing, quality, regulatory and commercial stakeholders, as well as external design and manufacturing partners, to ensure projects are delivered on time, within budget and to the highest quality standards.

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Job Responsibilities that you be covering:

• You will lead multidisciplinary medical device development projects, providing technical leadership and mentorship while acting as a key device development representative across internal and external stakeholder groups.
• You will manage the full device development lifecycle, from concept evaluation and specification development through design, design control, risk management, verification, validation and industrialisation activities.
  
  You will coordinate activities with external design, development and manufacturing partners, ensuring successful project delivery against quality, cost and timeline objectives.
• You will support human factors and usability studies, contribute to combination product development programmes and help develop innovative healthcare solutions that improve patient outcomes.
• You will contribute to complaint investigations, technical issue resolution and design change control activities, ensuring compliance with quality, regulatory and continuous improvement requirements.
• You will support supplier assessments, capability evaluations, regulatory submissions and the preparation of technical documentation to maintain the highest standards of quality and compliance.

What skills, qualifications and experiences you will hold as an Medical Device Development Specialist:

• You will hold a degree in Chemical Engineering or a related scientific or engineering…