Device Project Coordinator

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!

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This is a full time, permanent position working 37 hours per week flexibly between 07:00 – 19:00.

As a Device Project Coordinator you will provide project management support to parenteral combination product developments.

Job Responsibilities that you be covering:

• You will support the Device Development Lead in managing day-to-day project activities, ensuring quality, cost and schedule targets are achieved in line with Eurofins standards.
• You will coordinate and contribute to the development of drug delivery devices, supporting project delivery through established procedures, processes and best practices.
• You will collaborate with multi-disciplinary teams to drive device development projects and lifecycle management activities from concept through to implementation.
• You will support the introduction and continuous improvement of drug delivery devices, ensuring activities are delivered efficiently and in compliance with project requirements.
• You will liaise with internal and external stakeholders to facilitate effective communication, alignment of objectives and successful project outcomes.
• You will work closely with development, manufacturing and technical teams to support device implementation, lifecycle management and ongoing operational excellence.

What skills, qualifications and experiences you will hold as an Device Project Coordinator:

• You will hold a BSc or MSc in a relevant science or engineering discipline, with experience within the pharmaceutical combination product and/or medical device industry and an understanding of project management methodologies and tools.
• You will have experience working within regulated environments and a strong understanding of ISO 13485, ISO 14971, 21 CFR 820, 21 CFR 4, the EU Medical Devices Regulation and Good Manufacturing Practice (GMP) requirements.
• You will have experience in design controls for combination products, preferably relating to parenteral drug delivery systems, alongside expertise in device risk management.
• You will have knowledge of Human Factors Engineering…