Regulatory Affairs Specialist – Medical Devices –

Carrot Recruitment; Manchester; On-site; GBP 40,000 - 60,000; Full time

Job summary

A leading recruitment firm is seeking a Regulatory Affairs Specialist for medical devices in Manchester. The role involves creating technical files, ensuring compliance with regulations, and responding to regulatory queries. The ideal candidate will possess extensive regulatory experience in the medical device sector.

Qualifications

• Experience in Regulatory Affairs within medical devices is required.

Responsibilities

• Creating technical files for a range of medical devices.
• Conducting gap analysis and revision of existing documentation.
• Responding to regulatory affairs queries.

Skills

Regulatory Affairs

Job description

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Regulatory Affairs Specialist – Medical Devices –, Manchester

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Client:

Carrot Recruitment

Location:

Manchester, United Kingdom

Job Category:

Other

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EU work permit required:

Yes

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Job Reference:

e42745eeeb18

Job Views:

5

Posted:

02.06.2025

Expiry Date:

17.07.2025

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Job Description:

The Role

As the Regulatory Affairs Specialist, you will be responsible for;

• Creating technical files for a range of medical devices, both new and existing devices
• Perform gap analysis and revision of existing documentation to ensure compliance with MDR
• Respond to and internal or external regulatory affairs queries

You

As the Regulatory Affairs Specialist, you will have the following experience:

• Regulatory Affairs experience within medical devices