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- Tasks: Lead quality management and ensure compliance in medical device production.
- Company: Innovative tech business in the medical device sector.
- Benefits: Competitive salary, career growth, and a chance to make a difference.
- Other info: Dynamic role with opportunities to engage with regulatory bodies.
- Why this job: Join a team that drives innovation and ensures product safety.
- Qualifications: Experience in Quality Assurance and regulatory affairs in medical devices.
The predicted salary is between 50000 - 65000 £ per year.
My client, an innovative technology business within the medical device sector, are seeking a Quality Assurance & Regulatory Affairs Manager to join their team.
- Leading and developing the company’s Quality Management System
- Ensuring effective quality control processes across materials and finished products
- Driving compliance across risk management, CAPA and audit activities
- Supporting regulatory submissions and maintaining compliance across EU and US markets
- Acting as a key contact for regulatory bodies and external stakeholders
- Managing post-market activities, including complaints and ongoing product compliance
- Strong experience within Quality Assurance / Regulatory environments
- Background within medical devices, diagnostics or a regulated manufacturing setting
You are welcome to contact our office or email us to discuss other opportunities.
Quality Assurance/ Regulatory Affairs Manager, Medical Devices in Cambridge employer: Eclectic Recruitment
Contact Detail:
Eclectic Recruitment Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Quality Assurance/ Regulatory Affairs Manager, Medical Devices in Cambridge
✨Tip Number 1
Network like a pro! Reach out to folks in the medical device sector on LinkedIn or at industry events. We all know that sometimes it’s not just what you know, but who you know that can land you that Quality Assurance role.
✨Tip Number 2
Prepare for those interviews by brushing up on your knowledge of regulatory compliance and quality management systems. We suggest you have some real-life examples ready to showcase your experience in driving compliance and managing audits.
✨Tip Number 3
Don’t forget to follow up after interviews! A quick thank-you email can go a long way. We recommend mentioning something specific from your conversation to remind them why you’re the perfect fit for their team.
✨Tip Number 4
Keep an eye on our website for openings! We regularly update our listings, and applying directly through us can give you a better chance of standing out. Plus, we’re always here to help you navigate the job search process.
We think you need these skills to ace Quality Assurance/ Regulatory Affairs Manager, Medical Devices in Cambridge
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Quality Assurance and Regulatory Affairs role. Highlight your experience in managing quality systems and compliance, especially in the medical device sector. We want to see how your background aligns with what we're looking for!
Showcase Relevant Experience: When writing your application, focus on your strong experience within Quality Assurance and Regulatory environments. Share specific examples of how you've driven compliance and managed audits, as this will really catch our eye.
Be Clear and Concise: Keep your application clear and to the point. Use bullet points where possible to make it easy for us to read through your qualifications and achievements. We appreciate a well-structured application that gets straight to the good stuff!
Apply Through Our Website: Don’t forget to apply through our website! It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it shows us you’re keen on joining our innovative team!
How to prepare for a job interview at Eclectic Recruitment
✨Know Your Quality Management Systems
Make sure you brush up on your knowledge of Quality Management Systems, especially those relevant to medical devices. Be ready to discuss how you've led or developed such systems in the past, as this will show your expertise and fit for the role.
✨Understand Regulatory Compliance
Familiarise yourself with the regulatory requirements for both EU and US markets. Prepare examples of how you've successfully navigated compliance challenges in previous roles, as this will demonstrate your capability to manage regulatory affairs effectively.
✨Showcase Your Problem-Solving Skills
Be prepared to discuss specific instances where you've driven compliance across risk management, CAPA, and audit activities. Highlight your analytical skills and how you've resolved issues, as this is crucial for a Quality Assurance/Regulatory Affairs Manager.
✨Engage with Stakeholders
Think about your experience acting as a key contact for regulatory bodies and external stakeholders. Be ready to share how you've built relationships and communicated effectively, as this will be important for managing post-market activities and ongoing product compliance.