Medical Device Quality & Regulatory Engineer — Global Travel

Crux Product Design; Bristol; On-site; GBP 40,000 - 60,000; Full time

Job summary

A leading consultancy in medical device development is seeking a Quality & Regulatory Engineer in Bristol. This role involves ensuring compliance with medical device standards, supporting the QMS, and contributing to impactful global projects. The ideal candidate has a relevant degree and strong experience in quality assurance and regulatory compliance. Opportunities for mentorship and collaboration are integral to the role, fostering a culture of curiosity and integrity.

Qualifications

• Experience in Medical Device Quality Assurance and Regulatory Compliance.
• Knowledge of IEC 62366-1, ISO 14971, EU MDR, and FDA guidance.

Responsibilities

• Embed quality throughout product development.
• Support validation of QMS systems.
• Contribute to risk management activities.
• Develop training materials for quality awareness.

Skills

Medical Device Quality Assurance

Regulatory Compliance

Analytical skills

Problem-solving

Attention to detail

Communication

Education

Relevant scientific/healthcare-related degree (Masters preferred)

Job description

A leading consultancy in medical device development is seeking a Quality & Regulatory Engineer in Bristol. This role involves ensuring compliance with medical device standards, supporting the QMS, and contributing to impactful global projects. The ideal candidate has a relevant degree and strong experience in quality assurance and regulatory compliance. Opportunities for mentorship and collaboration are integral to the role, fostering a culture of curiosity and integrity.