We’re looking for an experienced Quality Manager or Regulatory Manager to join an incredible Oxford-based medical technology company.
What will I be doing?
Working closely with the heads of departments, and reporting directly to the CEO, you will have day-to-day responsibility for the Quality Management System, designing, implementing and maintaining ISO 13485-ready processes and documentation, as well as ensuring that all staff are trained in and adhering too, the QMS.
You will also be responsible for the preparation of documentation to support clinical trials, and will lead on the evaluation, selection and implementation of an eQMS.
About the company
Spun-out of an existing, successful scientific R&D firm over 5 years ago, you will be joining a talented and dedicated team as they continue to develop proof of principle technology into a fully functioning MHRA-approved product prototype. Using ultrasound technology, the company has developed a novel, minimally-invasive surgical procedure that has the potential to transform spinal surgery.
The ideal candidate will have…
This is an excellent opportunity you to make the next step on your career and to embrace a new challenge.
If you’re interested in the role then please apply now for immediate consideration.
Alternatively, if you’re not ready to apply just yet but would like some more information, please feel free to call me on 07733017601 or email email@example.com