SRG are currently looking for a Regulatory Affairs Specialist at various levels of seniority for a renowned Medical Device client based just in the North...
SRG are currently look for a Quality Manager for a client based in South East of England. Salary on offer is dependent on experience and benefits are very competitive. They client is a major player in the manufacture of Medical Devices.
This job will require you to:
- Manage the ISO 13485 QMS.
- Lead the internal auditing process
- Develop, maintain and carry out quality training
- Educated to degree level
- Sound knowledge of working within an ISO 13485 QMS
- Grasp of compliance with MDD and FDA regulations
- Experience with Technical Files, Design master files,
- Medical Device master files and 510(k) submissions.
If you feel like you fit the description please apply to this advert or alternatively you can contact Feroze Malik on 0161 868 22 33 or email me on .
The recruiter has stated that all applicants for this job should be able to prove they are legally entitled to work in the UK. SRG is a trading name of Science Recruitment Group Ltd an Employment Business/Agency.