All jobs near Europe in the Regulatory sector

• Hampshire
• Negotiable
• Posted 4 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 8 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 10 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 22 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 22 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 29 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.

• Oberhonnefeld-Gierend
• Negotiable
• Posted about 2 months ago

We have a current opportunity for a Head of QA/RA on a permanent basis. The position will be based in Oberhonnefeld-Gierend. For further information about this position please apply. Job Summary: The Head of Quality and Regulatory Affairs will oversee and manage all quality and regulatory functio...

• Germany
• Negotiable
• Posted about 2 months ago

Job Description: Integrated Clinician - Medical Devices (Active & Non-Active) Location: Remote / Hybrid (Flexible) Employment Type: Contract / Permanent Industry: Medical Devices, Regulatory Affairs, Notified Body Key Responsibilities: Conduct clinical evaluations and assessments of active and no...

• Barcelona
• Negotiable
• Posted about 2 months ago

I am working with a highly innovative biotech company based in Barcelona, specializing in the development of groundbreaking medical devices. We are looking for a Regulatory Affairs & Quality Assurance Specialist to join their team. Ideal Profile: Experience in regulatory strategies and documentat...