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Senior Regulatory and Quality Assurance Expert (25680)

to £60k DoE with good benefits

Covering a variety of industries, including biomedical and engineering

This role, with a well-established company based in Cambridge, involves providing regulatory support to project teams, spanning both medical and non-medical disciplines, as well as supporting high level operational activities of the Quality Management System and other related management systems. This is a great opportunity to deepen your knowledge and gain experience across multiple industries.

This position offers a chance to further develop already established skills in leadership and project management. The role allows you to own meaningful contributions to global systems as a quality and regulatory technical lead. Ideally, you will already have strong experience in the regulatory field, and this role will offer you the chance to utilise this to provide a strategic advantage to projects whilst expanding our client’s knowledge and experience of European, US and Asian regulations (for both medical and non-medical applications). Your excellent communication skills will be called upon to interpret key regulatory changes and the implications for the team and wider business. You must be a proactive communicator and have the ability to take ownership of initiatives, deliver results, and strive for continual improvement.

You must understand and demonstrate the ability to balance the freedom to innovate, with rigour in the design process, by applying your knowledge and experience of quality management appropriately to each situation.

You will need to be a clear thinker, who can work independently, flexibly and inventively to support and inspire others, showing leadership in managing and undertaking activities.

You will be expected to have the following skills and experience for this role:

  • An excellent degree ( 2.1 or above from a Russell Group or similarly well respected university) in a STEM subject such as engineering or life sciences
  • The experience to interpret regulatory and standard requirements to ensure the downstream effects produce high quality results efficiently
  • A demonstrable track record of developing and executing global regulatory strategies that align with business needs and deliverables
  • Previous experience with medical devices is strongly preferred but not essential

A good benefits package will be offered to the successful candidate, including a profit share scheme in addition to a highly competitive basic salary.

Keywords: Quality, regulations, project management, leadership, communication, engineering, biomedical

Interested? Send your CV to ECM Selection; whilst we can only put forward the top few candidates, we do read every CV and try to respond to everyone. Or recommend a friend for £250, details at http://ecmselection.co.uk/tell-a-friend.

Please note: even if you don't have exactly the background indicated, do contact us now if this type of job is of interest - we may well have similar opportunities that you would be suited to. And of course, we always get your permission before submitting your CV to a company.