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For Companies At a Glance
- Tasks: Lead quality assurance in a global medical device company and ensure compliance with industry standards.
- Company: Global medical device manufacturer with a focus on quality and safety.
- Benefits: Competitive salary, bonus package, and opportunities for professional growth.
- Why this job: Make a real impact on quality and compliance in a dynamic environment.
- Qualifications: Experience in quality management within regulated sectors like medical devices or pharmaceuticals.
- Other info: Collaborative culture with opportunities to work across multiple sectors.
The predicted salary is between 60000 - 70000 £ per year.
Based Northern UK – M62 / M1 circa Manchester, Leeds, Sheffield, Doncaster - Office 2-3 times per week. 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.
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).
- 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.
- Laboratory & Product Quality Oversight
- 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.
- GMP & Audit Leadership
- 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.
- Experience leading and managing internal and external audits.
- Strong knowledge of risk management, CAPA processes, and regulatory compliance.
- Excellent organisational, leadership, and communication skills.
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.
Quality Assurance Manager in Sheffield employer: Progress Sales Recruitment Ltd
Contact Detail:
Progress Sales Recruitment Ltd Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Quality Assurance Manager in Sheffield
✨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 in past positions. 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 skills and experience. Plus, it shows you're serious about joining our team!
We think you need these skills to ace Quality Assurance Manager in Sheffield
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 standards, GMP, and any relevant audits you've led. We want to see how your background aligns with what we're looking for!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about quality assurance in the medical device sector. Share specific examples of how you've driven improvements in previous roles — we love a good story!
Showcase Your Leadership Skills: As a QA Manager, you'll be leading teams and driving a culture of quality. Make sure to highlight your leadership experience and how you've successfully managed teams or projects in the past. We’re keen to see your proactive approach!
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you don’t miss out on any important updates. Plus, it shows you're serious about joining our team!
How to prepare for a job interview at Progress Sales Recruitment Ltd
✨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 expertise and understanding of the regulatory landscape.
✨Showcase Your Leadership Skills
Prepare examples that highlight your leadership experience, especially in managing audits and compliance. Discuss how you've led teams through challenges and improved quality systems, as this will demonstrate your capability to drive a culture of quality.
✨Engage with Technical Questions
Expect technical questions related to QA testing processes and document control. Brush up on your knowledge of CAPA processes and risk management, and be prepared to explain how you’ve handled these in past roles.
✨Demonstrate Your Collaborative Spirit
Since the role involves working closely with laboratory teams, be ready to discuss how you’ve successfully collaborated across functions. Share specific instances where your teamwork led to improved quality outcomes or compliance.