Device Development Quality Lead

3 weeks ago


Cambridge, Cambridgeshire, United Kingdom Russell Tobin Full time

We are seeking a highly skilled Device Development Quality Lead to join our team in Cambridge, UK.

About the Role:

This is a full-time position that requires a minimum of 5 days per fortnight on-site in Cambridge.

Responsibilities:
  • Support internal and external audits of the DCoE Quality Management System.
  • Support the assessment of external design companies and suppliers for capability of quality systems, facilities, and procedures to support device development and supply.
  • Provide input and support to design validation including human factors engineering assessments.

We offer a competitive salary of £46,000 - £57,000 per annum, depending on experience, and a PAYE rate max up to £23.18 p/h and Umbrella rate max up to £26.12 p/h.

Requirements:
  • BSc in an appropriate science & engineering discipline (chemistry, biology, biomedical sciences, mechanical engineering, materials sciences, chemical engineering; or other related discipline) with a minimum of 2 years of relevant experience.
  • MSc in an appropriate science & engineering discipline (chemistry, biology, biomedical sciences, mechanical engineering, materials sciences, chemical engineering; or other related discipline) with a minimum of 2 years of relevant experience.
  • PhD in an appropriate science & engineering discipline (chemistry, biology, biomedical sciences, mechanical engineering, materials sciences, chemical engineering; or other related discipline).
Skills and Qualifications:
  • Familiarity with 21 CFR 820 and the EU Medical Devices Regulation.
  • Able to prioritize multiple responsibilities and to work on multiple tasks simultaneously.
  • High level of attention to technical details and accuracy.


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