At a Glance
- Tasks: Lead quality management for innovative medical device projects and ensure compliance with regulations.
- Company: Join Ensera Design, a top consultancy in user-centred innovation for health sectors.
- Benefits: Enjoy flexible working, private healthcare, and generous annual leave.
- Other info: Collaborative culture with opportunities for personal and professional growth.
- Why this job: Make a real impact in healthcare by ensuring high-quality product development.
- Qualifications: Senior-level experience in medical devices and strong communication skills required.
The predicted salary is between 51000 - 73954 ÂŁ per year.
Ensera Design is a world-class user‑centred innovation and product development consultancy, specialising in the medical and consumer health sectors with offices in Bristol, Colorado and New Jersey. As part of Ensera, we collaborate globally with contract manufacturing facilities in Europe, the USA, and Asia. We are currently seeking an experienced Senior Design Quality Engineer to join our talented team and contribute to delivering exceptional solutions for our clients.
The role will be responsible for the day‑to‑day management, oversight, and continuous improvement of Quality activities. This role ensures all quality related activities are executed in compliance with applicable EU MDR, EMA, and FDA regulations, including 21 CFR Parts 820, 210, 211, internal procedures, customer requirements and all other industry applicable regulations and standards.
Responsibilities:
- You will partner with electromechanical and software engineering and design teams to deliver new products to market in compliance with required quality requirements and processes.
- You will guide project teams through consistent, compliant and lean delivery according to Design Control and Risk Management processes.
- You will provide clear updates to stakeholders across the business and provide guidance on project readiness.
- You will develop, maintain complete and compliant Design History Files and support the development of regulatory submissions for new products including pre‑submission, 510(k) and other product required regulatory submissions.
- You will interface with external regulatory experts and clients to drive collaborative delivery of Design History Files.
- You will support the continual improvement of Quality System processes and tools that support the product development process.
- You will provide coaching and training to other teams relating to Design Control processes and continuous improvement.
- You will support our quality and delivery teams with carrying out QMS and project audits when required including participation as a subject matter expert when required.
About you:
You’ll be working already at a senior level either in Consultancy, or industry, or at a start‑up within the medical device and medicinal products sector. You’ll be comfortable taking the lead in large project teams in complex medical device development, ready to collaborate with Software, Electronic and Mechanical Engineers, Designers, and Manufacturing experts.
Skills and experience:
- Either a degree in a relevant engineering, design or science discipline (or equivalent qualification – Advanced degree preferred), or equivalent work experience.
- Demonstrable experience of progressive quality and hands‑on experience in a regulated environment, supporting medical devices, or pharmaceuticals operations (we think someone with between 5 and 8 years of experience is likely to have the level of competence we are looking for).
- Experience guiding teams through compliant development of medical Software and complex electromechanical systems.
- Experience in interfacing with multiple internal and external stakeholders and driving high quality work to meet their needs.
- Experience contributing to the development of Quality Management Systems and the ability to interpret regulations.
- Experience ensuring a high level of compliance with MDR, ISO 13485, 21 CFR 820, and cGMP.
- Experience in Risk Management tools and techniques (ISO14971).
- Experience in IEC62304, and IEC 60601 would be desirable.
- Experience in auditing to ISO 13485 would be desirable.
- Able to review and understand hardware, firmware and software requirements and specifications.
- Excellent communication and interpersonal skills.
- Excellent presentation skills including written and verbal communication skills.
Salary: The salary for this role is in line with our Senior band, from £51,000 up to £73,954. Please note we ask you to provide your expected salary within the band as part of your application, this helps us understand how you view your experience against the role’s scope.
Why work with us:
Ensera Design offers interesting and varied work combined with a supportive team culture to provide a stimulating environment where you will have the opportunity to develop and learn from others. We offer flexible working policies where working patterns are agreed with our line managers, taking into account the role, needs of the individual, and the team. We recognise that we are only as good as our people and we know how important it is to support our team.
Benefits:
- Performance‑related company‑wide bonus.
- Flexible hybrid working in line with our core hours (Mon–Thu, 9:30am–12:00pm & 2:00pm–4:00pm; Fri, 9:30am–12:00pm).
- Private healthcare for you and your family.
- Enhanced maternity and paternity leave.
- Salary exchange pension scheme.
- 25 days of annual leave, plus the option to purchase up to one working week and additional days for length of service.
- Access to our Employee Assistance Programme and digital wellbeing platform.
- Cycle to Work & Electric Vehicle Lease schemes.
- Death in service (x4 gross salary).
- Training and development opportunities, including dedicated learning days and regular knowledge‑sharing sessions.
- A free lunch the first Monday of every month alongside our company‑wide meeting.
- Free breakfast every Wednesday, and plenty of opportunities to socialise, including team‑organised activities, summer and Christmas parties, and more.
About us:
We are based in an iconic Grade II listed building in the heart of Bristol. Our vibrant workspace houses state‑of‑the‑art labs, a design studio, usability suites, and collaborative meeting spaces. Nestled in a lively neighbourhood with independent shops, we’re just a short walk from Park Street, the Harbourside, and St. Nick’s Markets.
Our values:
- Find a way: We work as one team, combining our knowledge and experience to unite around a shared goal. We trust each other and do what’s needed to get things done and exceed expectations.
- Pull together: We believe anything is possible. When faced with challenges we take the initiative, using our creative spirit and determination to find bold solutions and deliver results that move us forward.
- Care: We act with integrity, take pride in our work, and support each other. We each play our part to make a positive impact for our customers, our colleagues, and our planet.
At Ensera Design we believe that designing for people means including all people, starting with the team behind the work. Our human‑centred design ethos is rooted in empathy, and our values – pull together, find a way, and care – guide us in building a team that reflects the diversity of the world we design for. We know that different perspectives lead to better ideas, stronger collaboration, and more meaningful outcomes. If you meet the skills and experience for this role, we welcome your application – whatever your background, identity, or path into design. What matters to us is that you share our belief in purposeful, people‑first design.
Senior Design Quality Engineer in Bristol employer: Ensera Design
Contact Detail:
Ensera Design Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Design Quality Engineer in Bristol
✨Tip Number 1
Network like a pro! Reach out to your connections in the medical device sector and let them know you're on the hunt for a Senior Design Quality Engineer role. You never know who might have the inside scoop on openings or can put in a good word for you.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of EU MDR, FDA regulations, and quality management systems. Be ready to discuss how you've successfully navigated these in past roles. Show us that you’re not just familiar with the rules but can apply them effectively!
✨Tip Number 3
Don’t forget to showcase your collaborative spirit! Highlight experiences where you’ve worked with cross-functional teams, especially with engineers and designers. We want to see how you can pull together with others to deliver high-quality results.
✨Tip Number 4
Apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, it shows us you’re genuinely interested in joining our team at Ensera Design. Let’s make it happen!
We think you need these skills to ace Senior Design Quality Engineer in Bristol
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Senior Design Quality Engineer role. Highlight your relevant experience in quality management and compliance with regulations like EU MDR and FDA. We want to see how your background aligns with what we do at Ensera!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about this role and how your skills can contribute to our team. Don’t forget to mention any specific projects or experiences that relate to medical devices or quality systems.
Showcase Your Communication Skills: Since excellent communication is key for this role, make sure your application reflects that. Use clear and concise language, and don’t shy away from showcasing your interpersonal skills. We love candidates who can articulate their thoughts well!
Apply Through Our Website: We encourage you to apply through our website for a smoother process. It helps us keep track of applications and ensures you’re considered for the role. Plus, it’s super easy – just follow the prompts and submit your materials!
How to prepare for a job interview at Ensera Design
✨Know Your Regulations
Familiarise yourself with the key regulations like EU MDR, FDA guidelines, and ISO standards relevant to the role. Be prepared to discuss how your experience aligns with these regulations and how you’ve ensured compliance in past projects.
✨Showcase Your Collaboration Skills
Since the role involves working closely with various teams, be ready to share specific examples of how you've successfully collaborated with engineers and designers. Highlight any challenges you faced and how you overcame them to deliver quality results.
✨Prepare for Technical Questions
Expect technical questions related to Design Control and Risk Management processes. Brush up on your knowledge of tools like ISO 14971 and IEC62304, and be ready to explain how you've applied these in your previous roles.
✨Demonstrate Continuous Improvement Mindset
Discuss your approach to continuous improvement in Quality Systems. Share examples of how you've implemented changes that enhanced processes or outcomes, and be prepared to suggest ideas for how you could contribute to Ensera's quality initiatives.