Parenteral Drug Delivery Devices Project Coordinator

Eurofins Sverige AB; United Kingdom; À distance; GBP 42 000 - 54 000; Plein temps

Avantages offerts par ce poste

Life Assurance from day one

Company Pension after 3 months

Perkbox access

Health Cash Plan

Résumé du poste

Eurofins is seeking a Device Project Coordinator to support parenteral combination product developments and device lifecycle management. The role involves coordinating development with cross-functional teams, ensuring quality, cost and schedule targets are met in line with Eurofins standards.

You will work closely with development, manufacturing and technical teams to drive device implementation and continuous improvement, while navigating regulated environments and GMP requirements.

Qualifications

• Experience in regulated environments and understanding of GMP/Medical Device standards.
• Knowledge of ISO 13485, ISO 14971, 21 CFR 820, and EU Medical Devices Regulation.

Responsabilités

• Provide project management support for parenteral combination product developments.
• Coordinate development of drug delivery devices and manage lifecycle activities.
• Collaborate with multi-disciplinary teams to drive device development projects from concept to implementation.
• Support introduction and continuous improvement of device processes ensuring compliance.
• Liaise with internal and external stakeholders to align objectives and outcomes.
• Work with development, manufacturing and technical teams to support device implementation and operational excellence.

Connaissances

Project management

Regulated environments

ISO 13485 knowledge

Communication skills

Attention to detail

Cross-functional collaboration

Formation

BSc or MSc in science or engineering

Outils

MS Office

Description du poste

Eurofins is seeking a Device Project Coordinator to support parenteral combination product developments and device lifecycle management. The role involves coordinating development with cross-functional teams, ensuring quality, cost and schedule targets are met in line with Eurofins standards.

You will work closely with development, manufacturing and technical teams to drive device implementation and continuous improvement, while navigating regulated environments and GMP requirements.