Regulatory Compliance & Quality Systems Manager

Job Details

A Global Pharmaceutical company are presently looking to bring in a Regulatory Compliance & Quality Systems Manager, within their medical devices division, to be based in their Berkshire Office for a 6 month contract.

Role:

- Coordinate and support regulatory activities across UK / Ireland.
- UK & Ireland Regulatory Requirements.
- Post Marketing Surveillance.
- Vigilance Reporting.
- Competent Authority Relationships.
- Field Safety Corrective Actions.
- Support Pre-market Activities.
- Quality System.

Experience:

- Experience of medical device regulations in UK / Ireland.
- Previous experience in the implantable medical device industry preferred.
- Knowledge of ISO 13485, ISO 9000 and / or ISO 14001.

To Apply:

To apply, please click on the Apply button. Ideally, please include a short note outlining why you are interested in the role and why you think you are suitable.

In case you have difficulty in applying or if you have any questions, please call me (Elise Lambeth) on +44 (0) 207 440 0633 or upload your CV on our website. Full description available on request.

Please note that not all of our vacancies are advertised. To register as a priority candidate, please upload your CV on our website with a short description of what you are looking for or call 0800 988 4437. We will then contact you with relevant roles: www.proclinical.co.uk. We regard all correspondence as confidential.

Proclinical is a specialist Employment Agency and Recruitment Business, providing employment opportunities within major companies in the Pharmaceutical and Biopharmaceutical industries across Europe.