Director of Quality (UK)

Cambridge, UK

Biofidelity’s mission is to improve and extend cancer patients’ lives by enabling better targeting of therapies, early detection of treatment resistance, and routine monitoring of treatment response. Our unique technology is designed to allow rapid, broad adoption of our assays in testing labs around the world, enabling a step change in patient care. 

At Biofidelity we are proud to have built a culture of teamwork, openness and trust. We work towards well-defined goals, with a strong belief that we can bring real benefits to patients. Our people are keen to take responsibility for their work and share both their successes and challenges. 

Alongside a competitive salary, we offer a comprehensive benefits package including private medical care, share option scheme, pension, cycle to work scheme, 26 days per year holiday allowance and free physical training sessions.

The role

Biofidelity is seeking an experienced and efficient Director of Quality to build and maintain a Quality Management System (QMS) to meet ISO 13485 requirements. Reporting to the Chief Operating Officer, the Director of Quality will be responsible for the Quality Management System and Quality Assurance function across Biofidelity’s UK and US sites.

Key responsibilities:

  • Delivering and maintaining a QMS for ISO 13485 and Biofidelity’s CLIA/CAP laboratory

  • Promote awareness of applicable regulatory requirements, QMS requirements, and customer requirements throughout the organisation

  • Developing and delivering training across the company 

  • Planning, initiating and managing quality improvement projects

  • Supporting the product development and software development teams with design control and risk management

  • Supporting investigations and complaint handling

  • Ensuring supplier and subcontractor compliance to Biofidelity requirements

  • Acting as a point of contact with certification authorities, including arranging and planning for assessments

  • Assisting with drafting and compilation of product documentation for regulatory submissions

Knowledge, Skills and Abilities:

  • Previous implementation and/or maintenance of an ISO 13485 QMS

  • Knowledge and demonstrated experience with LDTs and IVDs

  • Working knowledge of other applicable standards including 21 CFR 820, 21 CFR Part 11, IEC 62304, ISO 14971, GAMP5, CAP and CLIA

  • Excellent organisational, communication and leadership skills 

  • Results-oriented, with strong attention to detail

Requisite Education and Experience / Minimum Qualifications:

  • Degree in science, medical or technical field

  • Proven industry experience in a regulated environment e.g. ISO 13485, ISO 15189, or ISO 17025

To apply, please email your CV and cover letter to

For informal enquiries about the post, please contact Ana Kukic, HR Business Partner,


How to apply

To register your interest, please send your CV to:

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Strictly no agencies. Only direct applicants will be considered for this role.

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