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Are you passionate about shaping the future of medical device quality? Join a team of expert engineers and human factors specialists driving innovation for the world’s leading pharmaceutical and device companies.
We’re hiring in our Bristol office for a role that blends quality management and regulatory awareness to ensure that device development activities align with the latest guidelines.
At Crux, we believe that curiosity drives innovation. As a specialist consultancy at the forefront of medical device development, we deliver safe, user-centred solutions that transform healthcare globally. We’re looking for an experienced and passionate Quality & Regulatory Engineer to join our growing team and support impactful work across a diverse portfolio of global projects.
Why Crux?
Work with top pharma clients on cutting-edge medical device projects.
Collaborate with a multidisciplinary team across our Bristol (UK) and Boston (US) offices.
Travel opportunities to support global project delivery
Influence the development of life-changing healthcare technologies
Be part of a consultancy that values curiosity, integrity, and collaboration
As a Quality & Regulatory Engineer, you’ll help maintain and improve our ISO‑certified QMS across human factors, device development, risk management, system validation, and sustainability. You will:
Embed quality throughout product development.
Support validation of QMS systems.
Support audits and change control.
Contribute to risk management activities.
Develop training materials to strengthen quality awareness.
A good degree in a relevant scientific/healthcare-related discipline (preferably Masters level).
Strong relevant sector experience in Medical Device Quality Assurance and Regulatory Compliance.
Awareness of medical device related standards, regulations and guidelines (IEC 62366-1, ISO 14971, EU MDR, and FDA guidance)
Strong analytical and problem-solving skills.
Excellent attention to detail and organisational skills.
Effective communication skills and the ability to work within a collaborative team environment.
Experience in technical documentation and regulatory submissions.
Confident communicator and proactive problem-solver.
Passion for mentoring and knowledge sharing.
Up-to-date with industry trends and best practices.
Curious, collaborative, and committed to making a difference.