At a Glance
- Tasks: Lead Quality Assurance activities and drive continuous improvement in a dynamic environment.
- Company: Join Medical Engineering Technologies, a trusted partner in the medical device industry.
- Benefits: Enjoy health cashback, private medical insurance, and clear career progression opportunities.
- Other info: Collaborate with international teams and shape quality systems across the organisation.
- Why this job: Make a real impact on quality culture while advancing your career in a global company.
- Qualifications: Experience in quality assurance, team leadership, and strong problem-solving skills.
The predicted salary is between 50000 - 60000 € per year.
Are you an experienced Quality Assurance professional looking for your next challenge? Do you have a keen eye for detail, a passion for building a strong quality culture and the drive to make a real impact? Here at Medical Engineering Technologies (MET Ltd), we’re looking for a proactive and hands‑on Quality Assurance Manager to lead our Dover site, while working closely with quality leaders across the wider Cormica Group, including teams in Bradford, Gosport and our international locations in the USA and Germany. This is a highly visible role with genuine scope to shape systems, influence culture and drive continuous improvement both locally and across the wider organisation. If you’re ready to inspire a talented team of scientists and analysts while advancing your own career – this could be the opportunity for you!
About Us
At Cormica, we’re more than just a business – we’re a trusted partner to medical device and pharmaceutical manufacturers worldwide. We deliver analytical research, development and testing services that help bring safe and effective products to market faster, improving patients’ lives globally. With laboratories across the UK, Europe and the US, quality and innovation sit at the heart of everything we do.
The Role
- Lead and oversee Quality Assurance activities, ensuring compliance with ISO 17025, expected familiarity with GMP and FDA 21 CFR 820, and other regulatory requirements.
- Develop, implement and continuously improve quality systems, policies and SOPs.
- Manage audits, investigations, non‑conformances and supplier quality, driving effective corrective and preventive actions.
- Lead, coach and develop a team of Quality Specialists, fostering a culture of quality and accountability.
- Act as the Management Representative for regulatory matters and liaise with certification bodies.
- Support health, safety and risk management, ensuring compliance with applicable regulations.
- Collaborate with UK and international sites to align quality standards and share best practice.
What’s in it for You
- Medicash – a health cashback plan that helps cover the cost of everyday healthcare, including dental, optical and physiotherapy treatments.
- Private Medical Insurance (upon successful completion of probation).
- Ongoing professional development and clear career progression opportunities.
- The opportunity to contribute to a business that values quality, integrity and innovation.
- Free onsite parking.
What We’re Looking For
- Proven ability to manage multiple priorities in a fast‑paced environment.
- Experience with Six Sigma, Lean methodologies and data‑driven continuous improvement.
- Strong stakeholder engagement skills, with the ability to communicate complex information clearly.
- A proactive, analytical mindset with strong problem‑solving capabilities.
- Experience leading, mentoring and developing high‑performing teams.
- Excellent planning, organisational and project management skills.
- Confidence in representing the business externally and delivering presentations.
- A self‑motivated, resilient and ethical approach to leadership.
Onboarding
As part of our pre‑employment checks, the successful candidate will be required to undergo an Enhanced Disclosure and Barring Service (DBS) check. This is applied in line with our internal policies and commitment to maintaining high standards of integrity and trust. We assess all disclosures fairly and in accordance with applicable legislation, including the Rehabilitation of Offenders Act 1974.
Quality Assurance Manager - Dover, UK employer: Cormica® Medical Device & Pharmaceutical Testing
At Medical Engineering Technologies (MET Ltd), we pride ourselves on being a leading employer in the medical device and pharmaceutical sector, offering a dynamic work environment in Dover that fosters innovation and quality. Our commitment to employee growth is evident through ongoing professional development opportunities and a supportive culture that encourages collaboration across our international teams. With benefits like private medical insurance and a health cashback plan, we ensure our employees are well taken care of while making a meaningful impact on global healthcare.
Contact Detail:
Cormica® Medical Device & Pharmaceutical Testing Recruiting Team
StudySmarter Expert Advice🤫
We think this is how you could land Quality Assurance Manager - Dover, UK
✨Tip Number 1
Network like a pro! Reach out to your connections in the industry, attend relevant events, and don’t be shy about letting people know you’re on the hunt for a Quality Assurance Manager role. You never know who might have the inside scoop on an opportunity!
✨Tip Number 2
Prepare for interviews by researching MET Ltd and the Cormica Group. Understand their values, culture, and recent projects. This will help you tailor your responses and show that you’re genuinely interested in making an impact at their Dover site.
✨Tip Number 3
Practice your STAR technique for answering competency questions. Think of specific situations where you’ve demonstrated your skills in quality assurance, problem-solving, and team leadership. This will help you stand out as a candidate who can drive continuous improvement.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, it shows you’re serious about joining a company that values quality and innovation.
We think you need these skills to ace Quality Assurance Manager - Dover, UK
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Quality Assurance Manager role. Highlight your experience with ISO 17025, GMP, and FDA regulations, as well as any relevant leadership roles you've held. We want to see how your skills align with what we're looking for!
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to express your passion for quality assurance and how you can contribute to our culture at Cormica. Be sure to mention specific examples of how you've driven continuous improvement in past roles.
Showcase Your Achievements:Don’t just list your responsibilities; showcase your achievements! Use metrics and examples to demonstrate how you've made an impact in previous positions. We love seeing how you've led teams or improved processes!
Apply Through Our Website:We encourage you to apply through our website for the best chance of getting noticed. It’s the easiest way for us to keep track of your application and ensure it reaches the right people. Plus, it shows you're serious about joining our team!
How to prepare for a job interview at Cormica® Medical Device & Pharmaceutical Testing
✨Know Your Standards
Familiarise yourself with ISO 17025, GMP, and FDA 21 CFR 820 regulations. Being able to discuss these standards confidently will show that you understand the quality landscape and can navigate it effectively.
✨Showcase Your Leadership Skills
Prepare examples of how you've led teams in the past, particularly in fostering a culture of quality and accountability. Highlight specific instances where your leadership made a tangible impact on quality assurance processes.
✨Be Data-Driven
Demonstrate your experience with Six Sigma and Lean methodologies by discussing how you've used data to drive continuous improvement. Be ready to share metrics or outcomes from previous projects that illustrate your analytical mindset.
✨Engage with Stakeholders
Practice articulating complex information clearly and concisely. Think of examples where you've successfully engaged stakeholders, as this role requires strong communication skills to align quality standards across various teams.
