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Eurofins

Global lab testing and analytics network

Device Project Coordinator

Project ManagementConfirmed live in the last 24 hours
Full-timeCambridge, UKNo salary listedIn-person

About the Job

Requirements

  • Hold a Bachelor of Science or Master of Science in a relevant science or engineering discipline.
  • Have experience within the pharmaceutical combination product and/or medical device industry and understand project management methodologies and tools.
  • Have experience working in 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 requirements.
  • Have experience in design controls for combination products and expertise in device risk management.
  • Have knowledge of Human Factors Engineering and Usability Engineering principles, device assembly and manufacturing processes, and relevant standards including EN 62366, EN 60601, and EN 62304.
  • Be able to learn, apply, and follow established procedures consistently; work independently with minimal supervision; and maintain attention to detail and accuracy.
  • Have communication, presentation, and interpersonal skills, proficiency in standard computer applications, and the ability to prioritize multiple tasks while collaborating within cross-functional teams.

Responsibilities

  • Support the Device Development Lead in managing day-to-day project activities and ensuring quality, cost, and schedule targets are achieved in line with company standards.
  • Coordinate and contribute to the development of drug delivery devices, supporting project delivery through established procedures, processes, and best practices.
  • Collaborate with multidisciplinary teams to drive device development projects and lifecycle management activities from concept through implementation.
  • Support the introduction and continuous improvement of drug delivery devices, ensuring activities are delivered efficiently and in compliance with project requirements.
  • Liaise with internal and external stakeholders to facilitate communication, alignment of objectives, and successful project outcomes.
  • Work with development, manufacturing, and technical teams to support device implementation, lifecycle management, and ongoing operational excellence.

Desired Qualifications

  • Experience with design controls for combination products relating to parenteral drug delivery systems is preferred.

About the Company

Eurofins

Global lab testing and analytics network

Eurofins provides global laboratory testing and analytical services to verify the safety, authenticity, and quality of products across food, water, medicine, and the environment. It operates a network of more than 900 laboratories in over 60 countries, offering access to more than 200,000 analytical methods. Its product work involves running specialized tests—using chemistry, biology, and other scientific techniques—to confirm origin, composition, and compliance of samples, such as detecting wine fraud or contaminant presence. The company differentiates itself through its massive, distributed lab network and broad portfolio, enabling standardized testing at scale and fast turnaround across many industries, rather than relying on a single specialty or location. Its goal is to protect public health and safety by delivering accurate, comprehensive testing data and helping clients meet regulatory and quality requirements.

Company size
10,001+
Company stage
IPO
Headquarters
Luxembourg
Founded
1987

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