Device Project Coordinator — Parenteral Drug Delivery
Listed on 2026-10-16
-
Business
Regulatory Compliance Specialist
Eurofins Scientific is seeking a Device Project Coordinator to provide PM support for parenteral combination product developments. The role runs 37 hours/week, flexibly between 07:00–19:00, and involves coordinating device development from concept through implementation in a regulated environment.
The successful candidate will hold a science/engineering degree and have experience with GMP, ISO 13485, and design controls for drug delivery devices, with strong communication and cross‑functional
As a Device Project Coordinator — Parenteral Drug Delivery, you will play an important part at Eurofins in Cambridge, England, United Kingdom.
We aim to respond to suitable candidates as soon as possible.
Full responsibilities and requirements are described in the listing above.
Learn more about the Device Project Coordinator — Parenteral Drug Delivery role in the description above.
We appreciate your interest in this position.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).