If you an experienced medical devices project manager looking for a new challenge; an innovative start-up based in Cambridge wants you!
With a well planned business model which support innovation from the clinicians whilst ensuring a reliable flow of new and interesting projects. Their close professional links with the NHS, HEE and an angel investor they are well supported.
As the Project Manager you will be responsible for leading the successful delivery of product development projects to targets including scope, cost, schedule and quality. This involves stakeholder management, including reporting internally in addition to close collaboration with third parties such as NHS clinicians, academics, CRO's, CDMO's, CMO's and suppliers.
Skills and experience required:
- Track record of leading and managing full-lifecycle medical device product development projects e.g. from concept, through design and development, clinical trial, regulatory approval, stable manufacture and market launch
- Developing class I, IIa, IIb medical devices
- Demonstrate some knowledge of the UK, EU, US and other international medical device regulatory requirements e.g. MDD, MDR, FDA 510k, Risk Management (14971), Electrical Safety (60601), Software Lifecycle (62304) and sterile devices standards
- Ability to travel independently to venues around the UK at times and for durations required by the role.
Permanent role with salary to be discussed with the consultant.
If you are an ambitious, skilled professional and your CV reflects the key areas mentioned above then please apply as instructed on the website.
Alternatively, for more information on this role, please contact Dominic Cappell Dominic.Cappell@srg.co.uk /DD. 01223 607857/ WhatsApp +447776656210.
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