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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)
- Ensure audit readiness at all times and maintain accurate quality records.
- Manage document control, change control, and staff training compliance systems.
- Lead Management Review and report on key quality metrics and KPIs.
- One direct head reports into the QA Manager.
- 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 Doncaster 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 Doncaster
✨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! During interviews, share specific examples of how you've led audits or improved compliance processes. This will demonstrate your practical skills and leadership abilities.
✨Tip Number 4
Don't forget to apply through our website! We make it easy for you to find roles that match your expertise in quality assurance. Plus, we love seeing candidates who are proactive about their job search!
We think you need these skills to ace Qa Manager in Doncaster
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 mentioned in the job description.
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're the perfect fit for this role. Mention specific experiences that demonstrate your understanding of ISO standards and your hands-on approach to quality assurance. We love a good story!
Showcase Your Achievements: Don’t just list your duties; showcase your achievements! Use metrics where possible to illustrate how you’ve improved quality systems or compliance in previous roles. This will help us see the impact you've made in your past positions.
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. Plus, we love seeing applications come directly from our site!
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 understanding of the regulatory landscape.
✨Showcase Your Leadership Skills
Prepare examples that highlight your leadership experience, especially in managing audits and compliance systems. Discuss how you’ve driven a culture of quality and continuous improvement in past positions.
✨Engage with Technical Details
Be prepared to dive into specifics about QA testing processes and how you’ve collaborated with laboratory teams. This will demonstrate your hands-on experience and ability to integrate quality systems effectively.
✨Ask Insightful Questions
Prepare thoughtful questions about the company’s current QMS and their approach to compliance. This shows your genuine interest in the role and helps you assess if the company aligns with your values and expertise.