This is a high-impact Senior Quality Engineering role at an ambitious MedTech organisation that is transforming patient care through cutting-edge solutions.

They are now looking for a Senior Quality Engineer to play a critical role in ensuring the safety, compliance, and effectiveness of their products throughout the design and development lifecycle.

What Is In It For You

• Salary of £70,000 - £80,000
• Flexible UK working options
• Comprehensive benefits package
• Work on life-impacting technology that directly improves patient outcomes
• Be part of a collaborative, innovation-driven environment
• Influence product quality at a strategic level, not just process compliance

The Opportunity

• This is a high-impact position where you’ll act as a trusted partner to Engineering and Regulatory teams, ensuring that products are developed in line with global standards and best practices.
• You’ll be at the heart of product development, influencing decisions, identifying risks early, and enabling the delivery of safe and compliant medical devices.

What You’ll Be Doing

• Leading quality activities across design and development, ensuring compliance with internal processes and regulatory requirements
• Acting as a key contributor in design reviews, evaluating inputs, outputs, verification and validation activities
• Supporting and guiding teams on Design Controls, Risk Management, and usability considerations
• Reviewing and approving engineering changes, ensuring product safety and integrity are maintained
• Driving risk management activities (including hazard analysis and FMEA) in line with ISO standards
• Supporting nonconformance investigations and identifying trends to inform product improvements
• Leading or contributing to CAPA activities, ensuring effective resolution and prevention of issues
• Conducting internal audits and supporting external regulatory inspections
• Maintaining and improving Quality Management System (QMS) processes and documentation

What We’re Looking For

• Degree in Engineering, Quality, or a related discipline
• Strong experience in quality assurance within medical devices or regulated environments
• Proven background working with Design Controls and Risk Management
• Solid understanding of Quality Management Systems (QMS)
• Experience supporting new product development within regulated frameworks
• Knowledge of software within medical devices (SaMD) is highly desirable
• Strong communication skills with the ability to influence stakeholders at all levels
• A proactive, detail-oriented mindset with a passion for product safety and quality

Interested?

If you’re passionate about quality, safety, and making a real difference in healthcare technology, we’d love to hear from you.

Apply now or get in touch for a confidential discussion.

Bright Purple is an equal opportunities employer: we are proud to work with clients who share our values of diversity and inclusion in our industry.