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• Hampshire
• Negotiable
• Posted 3 days ago

Exciting Opportunity: EMC Test Technician / Engineer About the Role Are you passionate about cutting-edge technology and innovation? Join our team of EMC specialists, where you'll play a vital role in testing the latest devices across a variety of industries. As an EMC Test Technician or Engineer...

• Copenhagen
• Negotiable
• Posted 7 days ago

We are working with a leading pharmaceutical company based in Copenhagen that are dedicated to the development, manufacturing, and commercialisation of small molecule therapeutics. Their mission is to improve patient outcomes through innovative and high-quality products. We are seeking a detail-o...

• Neuchâtel
• Negotiable
• Posted 7 days ago

We are currently working with a leading pharmaceutical company looking for an EHS Director to join their team. This is an exciting opportunity to build a long-term career in a dynamic and innovative environment. You will be responsible for: Overseeing all environmental, safety, and industrial hyg...

• Paris
• Negotiable
• Posted 9 days ago

My client is building the first universal AI Operating System to lay the foundation for Biological Artificial Superintelligence (BASI). This OS integrates a suite of AI agents that decode complex biology, accelerate research, and dramatically increase productivity. Acting as copilots,My clients a...

• Paris
• Negotiable
• Posted 10 days ago

Job Title: Senior Regulatory Affairs Specialist Location: France (Hybrid) Start Date: Within the next month Job Type: Full-time (Consultant, Freelancer, or Contractor) Industry: Medical Devices Key Responsibilities: Documentation Specialist: Lead and manage all regulatory documentation processes,...

• Northern Ireland
• Negotiable
• Posted 21 days ago

We have a current opportunity for a Regulatory Affairs Specialist - IVDR on a contract basis. Please apply if you have the skill set and are interested: 6-12 months project Full time (39 hours per week) Hybrid Start - May/June IVDR Regulatory Knowledge, getting ready for clinical trials. GAP Asse...

• Northern Ireland
• Negotiable
• Posted 21 days ago

We have a current opportunity for a Regulatory Affairs Specialist - IVDR on a contract basis in Northern Ireland. Please apply if you have the skill set and are interested: 6-12 months project Full time (39 hours per week) Hybrid Start - May/June IVDR Regulatory Knowledge, getting ready for clini...

• Northern Ireland
• Negotiable
• Posted 28 days ago

We have a current opportunity for a Senior Clinical Project Manager working with IVDs on a contract basis. 6 months contract (possible extension) Clinical protocols, risk management plans, knowledge of IVD regulation within Europe Client-facing position (face-to-face) Remote with occasional site ...

• Freiburg im Breisgau
• Negotiable
• Posted about 1 month ago

We are looking for ambitious and motivated individuals who enjoy working in a dynamic and fast-growing environment. Together we want to further expand our customer and product portfolio and actively shape the future of medical technology. Regulatory Affairs Specialist (m/w/d) Your tasks: Internal...

• Nottingham
• Negotiable
• Posted about 1 month ago

We have a current opportunity for a Regulatory / Medical Writer on a contract basis for up to 40 hours per week. The position will be fully remote, dedicated to a renowned CRO. Experience within oncology is desired. Further information about this position please apply.