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For Companies At a Glance
- Tasks: Lead quality assurance in a dynamic medical device manufacturing environment.
- Company: Global leader in medical devices with a collaborative culture.
- Benefits: Competitive salary, bonus, and comprehensive benefits package.
- Why this job: Make a real impact on quality and compliance in healthcare.
- Qualifications: Experience in QA within medical devices or pharmaceuticals required.
- Other info: Opportunity for leadership and career growth in a regulated sector.
The predicted salary is between 60000 - 70000 £ per year.
Quality Assurance (QA) Manager for a medical device manufacturer based in Northern UK – M62 / M1 circa Manchester, Leeds, Sheffield, Doncaster. Base salary £60-70k (Negotiable) with Bonus and Package.
Role Overview
Our client is a global medical device manufacturer seeking an experienced and hands-on Quality Assurance Manager to lead their Quality function in a regulated manufacturing environment. This role is ideal for a Quality professional from the medical device, pharmaceutical, or chemical manufacturing sectors who can operate strategically and practically — including close collaboration with laboratory teams to support QA testing and compliance. The QA Manager will ensure regulatory compliance, maintain a robust Quality Management System (QMS), and drive a culture of quality, safety, and continuous improvement across the business. Office access required 2-3 days a week.
Key Responsibilities
- Quality Management & Compliance
- Lead, maintain, and continuously improve the QMS in line with:
- ISO 9001
- ISO 14001
- GMP standards (applicable to the sector)
- UK MDR (for medical device components, if applicable)
- Work closely with laboratory teams to oversee QA testing processes.
- Ensure handling, testing, and documentation of products meet regulatory and safety standards.
- Integrate quality systems within lab operations to maintain data integrity, traceability, and compliance.
- Support method validation, stability studies, and product testing as required.
- Lead internal and supplier audits, ensuring effective follow-up and closure of CAPAs.
- Prepare for and support external audits from certification bodies, MHRA, or other regulatory authorities.
- Implement and oversee GMP standards across production and laboratory operations.
- Maintain and develop HACCP systems where relevant.
- Ensure environmental compliance aligned with ISO 14001 standards.
- Monitor and drive improvements in environmental, safety, and quality performance.
Key Requirements
- Proven experience as a Quality Manager in medical device, pharmaceutical, or chemical manufacturing.
- Strong understanding of laboratory QA testing and ability to integrate with lab teams.
- Practical experience with:
- ISO 9001
- ISO 14001
- HACCP
- GMP standards
Personal Attributes
- Detail-oriented, proactive, and solutions-focused.
- Comfortable working strategically and hands-on.
- Confident engaging with auditors, regulators, and cross-functional teams.
- Committed to fostering a culture of compliance, accountability, and continuous improvement.
Why Join?
- Leadership role with visible impact on quality, compliance, and operational excellence.
- Opportunity to work across multiple regulated sectors — medical device, pharmaceutical, and chemical manufacturing.
- Collaborative culture with close integration between lab, production, and operations.
- Competitive salary and benefits package.
Qa Manager in Manchester employer: Progress Sales Recruitment
Contact Detail:
Progress Sales Recruitment Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Qa Manager in Manchester
✨Tip Number 1
Network like a pro! Reach out to your connections in the medical device or pharmaceutical sectors. Attend industry events or webinars to meet potential employers and get your name out there.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of ISO standards and GMP practices. Be ready to discuss how you've implemented quality management systems in your previous roles.
✨Tip Number 3
Showcase your hands-on experience! Bring examples of how you've led audits or improved compliance in past positions. This will demonstrate your practical skills and strategic thinking.
✨Tip Number 4
Don't forget to apply through our website! We have loads of opportunities that might be perfect for you, and applying directly can give you an edge over other candidates.
We think you need these skills to ace Qa Manager in Manchester
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the QA Manager role. Highlight your experience in quality management, especially in medical devices or pharmaceuticals. We want to see how your skills align with the key responsibilities listed in the job description.
Craft a Compelling Cover Letter: Your cover letter should tell us why you're the perfect fit for this role. Share specific examples of your past achievements in quality assurance and how they relate to the requirements of the position. This is your chance to show off your personality too!
Showcase Your Compliance Knowledge: Since compliance is a big deal in this role, make sure to mention your familiarity with ISO standards, GMP, and any relevant regulations. We want to know that you can keep our quality management system robust and audit-ready at all times.
Apply Through Our Website: We encourage you to apply through our website for a smoother application process. It helps us keep track of your application and ensures you don’t miss out on any important updates from us. Plus, it’s super easy!
How to prepare for a job interview at Progress Sales Recruitment
✨Know Your Standards
Familiarise yourself with ISO 9001, ISO 14001, and GMP standards before the interview. Be ready to discuss how you've applied these in your previous roles, as this will show your practical experience and understanding of regulatory compliance.
✨Showcase Your Leadership Skills
Prepare examples of how you've led teams or projects in quality assurance. Highlight your experience with audits and CAPA processes, as well as how you’ve driven a culture of quality and continuous improvement in past positions.
✨Engage with Technical Questions
Expect technical questions related to QA testing and laboratory operations. Brush up on your knowledge of risk management and document control systems, and be prepared to explain how you ensure audit readiness and maintain accurate quality records.
✨Demonstrate Collaboration
Since the role involves working closely with laboratory teams, think of examples where you've successfully collaborated across departments. Emphasise your communication skills and how you’ve integrated quality systems within lab operations to enhance compliance and data integrity.