Biocompatibility Expert
4 days ago
Cregg Group seeks a Biocompatibility Expert to lead our efforts in ensuring compliance with global medical device regulations, particularly ISO 10993. As a key member of our Regulatory Affairs department, you will be responsible for identifying and critically assessing emerging standards, theories, and methodologies.
The ideal candidate will have excellent knowledge of biocompatibility testing, including laboratory evaluations, and be able to provide expert guidance on biological safety processes.
Key Responsibilities:
- Lead the research, analysis, and communication of information pertaining to biocompatibility testing
- Provide expert guidance on biological safety processes
- Support development project teams on biocompatibility-related matters
Requirements:
- Level 8 Degree or Master's in Science or Engineering or similar
- Minimum of 3 years experience in a similar role in the medical devices industry
- Regulatory experience in Medical Devices, Pharmaceuticals, or similar regulated industry
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Regulatory Affairs Specialist
2 weeks ago
Ennis, Clare, Ireland Cregg Group Full timeRegulatory Affairs Specialist Excellent opportunity for a Senior Regulatory Affairs Specialist to join a thriving company in Co. Clare. The Senior Regulatory Affairs Specialist will be responsible for developing and implementing regulatory strategies to support the timely and successful registration, approval, and maintenance of company and client products....
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Senior Regulatory Affairs Specialist
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Ennis, Clare, Ireland Cregg Group Full timeSenior Regulatory Affairs Specialist Excellent opportunity for a Senior Regulatory Affairs Specialist to join a thriving company in Co. Clare.The Senior Regulatory Affairs Specialist will be responsible for developing and implementing regulatory strategies to support the timely and successful registration, approval, and maintenance of company and client...