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For Companies At a Glance
- Tasks: Lead global quality assurance strategies and ensure compliance with international standards.
- Company: Join Vernacare, a leading medical device company focused on innovation and quality.
- Benefits: Attractive salary, car allowance, pension, and opportunities for professional growth.
- Why this job: Make a real impact in healthcare by ensuring product safety and quality.
- Qualifications: Experience in quality management and strong knowledge of ISO 13485 required.
- Other info: Collaborative environment with passionate professionals dedicated to excellence.
The predicted salary is between 36000 - 60000 £ per year.
About Vernacare
Vernacare is a leading medical device company committed to delivering innovative, high-quality products that improve patient care and safety. With a strong global presence, we pride ourselves on excellence, compliance, and continuous improvement across all aspects of our operations.
The Role
We are looking for a highly experienced and driven Global Quality Assurance Manager to take ownership of our global quality assurance function across our medical device portfolio. This is not just a senior role—it is a fundamental pillar within our business, with the opportunity to make a real and immediate impact. You will be at the heart of ensuring our products meet international regulatory standards, exceed customer expectations, and uphold the highest levels of safety and quality. Your leadership will shape the future of our quality strategy, driving excellence across every stage of the product lifecycle. In this pivotal position, you will develop and implement global quality strategies, lead audits, support site managers, and champion continuous improvement initiatives. Your expertise in ISO 13485 and regulatory compliance will be essential, but equally important is your ability to lead from the front, inspire cross-functional teams, and embed a culture of quality throughout the organisation.
Key Responsibilities
- Lead global quality assurance strategies aligned with ISO 13485 and other relevant standards.
- Oversee and support internal and external audits (MDSAP, GMP, ISO 13485).
- Oversee ETO sterilisation processes and batch release protocols across product classifications (medical devices, biocides, cosmetics, pharmaceuticals).
- Maintain and improve quality management systems across product lifecycles.
- Collaborate cross-functionally with NPD, manufacturing, regulatory affairs, and procurement.
- Manage supplier quality and ensure compliance of incoming materials.
- Lead CAPA processes and root cause analysis using Six Sigma/Lean methodologies.
- Support site managers globally to ensure consistent quality standards.
- Conduct gap analyses for new acquisitions and implement quality improvement plans.
About You
You are more than just a quality expert—you are a leader who is passionate about making a real impact. You bring a strong foundation in medical device quality management, backed by hands-on experience with ISO 13485 and regulatory compliance. What truly sets you apart is your ability to inspire and elevate those around you. We are looking for someone who can mentor and develop a high-performing quality team, driving a culture of excellence and continuous improvement. If you are hungry to make a difference, thrive in a fast-paced environment, and lead from the front with confidence and clarity, this could be the perfect fit for you. You will be a trusted advisor across departments, a problem-solver with a strategic mindset, and a role model who leads by example. Your ability to communicate effectively, build strong relationships, and foster collaboration will be key to your success in this role.
Essential Criteria
- Bachelor's degree in a relevant field or equivalent experience.
- Minimum 3 years' experience in quality management within medical devices.
- Strong knowledge of ISO 13485, MDD/MDR, and GMP standards.
- Experience with Class I and II devices (sterile and non-sterile).
- Proven success in leading audits and CAPA initiatives.
- Excellent communication, presentation, and organisational skills.
- Fluent in English and proficient in Microsoft Office.
Desirable
- Experience in biocides, pharmaceuticals, or cosmetics.
- Familiarity with AQL protocols and global quality strategy development.
Why Join Vernacare?
This is a unique opportunity to shape the global quality landscape of a respected medical device company. You will work with passionate professionals, contribute to meaningful innovation, and help ensure the safety and effectiveness of products used in healthcare settings worldwide.
Global Quality Assurance Manager in Worksop employer: Vernacare
Contact Detail:
Vernacare Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Global Quality Assurance Manager in Worksop
✨Tip Number 1
Network like a pro! Reach out to industry professionals on LinkedIn or attend relevant events. We can’t stress enough how important it is to make connections that could lead to job opportunities.
✨Tip Number 2
Prepare for interviews by researching the company and its products. Understand their quality assurance processes and be ready to discuss how your experience aligns with their needs. We want you to shine!
✨Tip Number 3
Practice your answers to common interview questions, especially those related to ISO 13485 and CAPA processes. We recommend doing mock interviews with friends or mentors to boost your confidence.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who are proactive about their job search.
We think you need these skills to ace Global Quality Assurance Manager in Worksop
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Global Quality Assurance Manager role. Highlight your experience with ISO 13485 and any relevant quality management achievements. 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 medical devices and how you can make an impact at Vernacare. Let us know what drives you and how you can inspire others.
Showcase Your Leadership Skills: Since this role is all about leading teams and driving quality initiatives, be sure to showcase your leadership experience. Share examples of how you've mentored others or led successful projects in your previous roles. We love seeing that kind of initiative!
Apply Through Our Website: We encourage you to apply through our website for a smoother application process. It helps us keep everything organised and ensures your application gets the attention it deserves. Plus, it’s super easy!
How to prepare for a job interview at Vernacare
✨Know Your Standards
Make sure you brush up on ISO 13485 and other relevant standards before the interview. Being able to discuss these in detail will show that you’re not just familiar with them, but that you can apply them effectively in a real-world context.
✨Showcase Your Leadership Skills
Prepare examples of how you've led teams or projects in the past, especially in quality assurance. Highlight your ability to inspire and mentor others, as this role requires someone who can elevate their team and drive a culture of excellence.
✨Be Ready for Technical Questions
Expect questions about audits, CAPA processes, and root cause analysis. Brush up on your Six Sigma and Lean methodologies, and be prepared to discuss how you've implemented these in previous roles to improve quality management systems.
✨Demonstrate Cross-Functional Collaboration
Think of examples where you've worked with different departments like NPD, manufacturing, or regulatory affairs. This role is all about collaboration, so showing that you can build strong relationships across functions will set you apart.
