Quality & Regulatory Engineer

CompanyCrux Product Design

LocationCity Of Bristol, England, United Kingdom

Posted At1/17/2026

UK Visa Sponsorship Analytics

Analytics are greyed out due to low classification confidence (53.0%).

Occupation Type

Quality assurance technicians

Occupation Code Skill LevelMedium Skilled

Sponsorship Salary Threshold

£41,700 (£21.38 per hour)

Standard minimum applies

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Description

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

Principal Responsibilities

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.

What We’re Looking For

Essential

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.

Desirable

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.

Why you'll love working here...

We are a dynamic and fast-growing design and engineering consultancy that takes pride in its outstanding work and warm and supportive workplace.

As part of our team, you’ll be working within a family of high-performing experts. Our strong community is built upon effective communication and happy employees, collaboration in project work and regular social events are the norm.

Check out what an opportunity at Crux offers you: Life at Crux