Regulatory Affairs Specialist
3 days ago
Cure Talent is proud to partner with a renowned Medical Device company that develops and distributes cutting-edge products. We are seeking an experienced Senior Regulatory Affairs Associate to join their team in West Yorkshire.
Key Responsibilities- Maintaining MDD & MDR compliance across the business
- Creating, reviewing, and updating Technical Files, PMS, and auditing reports
- Conducting Post-Market Surveillance activities
- Ensuring regulatory compliance with ISO 13485 standards
- Performing internal audits
- Proven track record in the Medical Device sector within a RA role
- Experience in Technical File management and creation
- Familiarity with MDD, MDR, and ISO 13485 regulations
The ideal candidate will have a strong background in regulatory affairs and be comfortable working in a fast-paced environment. If you're passionate about contributing to better patient outcomes, we encourage you to apply.
Estimated salary: £45,000 - £60,000 per annum, depending on experience.
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Long Lee, United Kingdom Cure Talent Full timeCure Talent is pleased to announce a job opening for a Senior Regulatory Affairs Associate at a reputable Medical Device company based in West Yorkshire. As part of our ongoing partnership, we seek a skilled professional to support the Regulatory Affairs Manager in maintaining compliance with industry standards.Responsibilities & RequirementsEnsuring MDD &...
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Medical Device Compliance Expert
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