Medical Devices Regulatory Affairs Manager - Medical Devices Jobs
Technology, Computers, Systems, Healthcare

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Covering the following locations: Edinburgh, Falkirk, Glasgow, Kilmarnock, Kirkcaldy, Motherwell, Paisley, Perth

Regulatory Affairs Manager

Are you an experienced QA / Regulatory professional, with a strong medical device background? If so, Zenopa has the role for you.

TITLE - Regulatory Affairs Manager
PRODUCTS - Patient Monitoring
LOCATION - Glasgow

In this exciting QARA Management role, you will be an integral part of the Operations team and will organise, plan, direct and control all Regulatory Affairs and Quality Management functions including product registration, complaint handling & reporting, internal and external quality audits.

Job Activities
- Develop, monitor, improve, and maintain documentation to ensure compliance with ISO13485 and FDA regulations such as CFR 820 and 21 CFR Part 11
- Provides guidance and support in Quality related matters across different departments.
- Liaise with supplier evaluation, selection and approval.
- Conduct internal, external, supplier audits and inspections.

Requirements
- BSc in Biomedical Engineering or relevant scientific discipline including Life Sciences/biomedical science.
- Capable of working independently and proactively.
- Good general IT skills and the ability to work with spreadsheets, word packages, PowerPoint etc.;
- Attention to detail
- Effective communicator
- Good analytical skills and critical thinking

Apply now to find out more about this exciting role.


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* Salary Guide
£Speak to Graham
Glasgow
Job Ref: 67125

Graham Auld

Medical Recruiter

graham@zenopa.com 01494 818 057

Why Zenopa?


Tags

patient monitoring equipment    gloves    drapes    needle    syringe    sharps    anaesthetics    gowns    sutures    hernia    medical pathology    poct    diagnostics    point of care    technology    computers    systems    medical    healthcare