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- Denmark
- Negotiable
- Posted 12 days ago
EPM Scientific are looking for a team of experienced consultants, to join our Medical Device client based near Copenhagen, Denmark. The initial project is focussed around a 510k submission, once completed focus will shift towards improving and maintaing compliance to ISO 13485. We are looking for...
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- England
- Negotiable
- Posted 17 days ago
Title: Regulatory Affairs Manager Summary: A leading global medical device company is seeking a Manager of Regulatory Affairs to join their innovative team. This key role involves managing regulatory submissions, including 510(k) filings, and working with both the US FDA and EU EMA to ensure comp...
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- Germany
- Negotiable
- Posted 23 days ago
Job Title: Labelling Specialist - Exciting Freelance Opportunity in Medical Device Sector Location: Germany (Remote/On-site) Leading medical device company committed to improving patient outcomes through innovative solutions. their products, including Class II medical devices, are used globally, ...
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- Switzerland
- Negotiable
- Posted about 2 months ago
Material Compliance Specialist - 6 month contract We are seeking a dedicated Material Compliance Specialist for an esteemed client within the dynamic Medical Device sector. This contract position, based in picturesque Switzerland, is perfect for someone with a keen eye on ensuring materials meet ...