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For Companies At a Glance
- Tasks: Lead global quality assurance strategies and ensure compliance across medical device products.
- Company: Join Vernacare, a leader in innovative medical devices committed to excellence.
- Benefits: Attractive salary, car allowance, pension, and opportunities for professional growth.
- Why this job: Make a real impact on patient care and safety in a dynamic environment.
- Qualifications: Experience in quality management and strong knowledge of ISO 13485 required.
- Other info: Collaborate with passionate professionals and shape the future of healthcare.
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’re 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’s a fundamental pillar within our business, with the opportunity to make a real and immediate impact. You’ll 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’ll 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 sterilization 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’re more than just a quality expert—you’re a leader who’s 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. But what truly sets you apart is your ability to inspire and elevate those around you. We’re looking for someone who can mentor and develop a high-performing quality team, driving a culture of excellence and continuous improvement. If you’re 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’ll 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’ll 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 employer: Vernacare
Contact Detail:
Vernacare Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Global Quality Assurance Manager
✨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. We want you to be able to discuss how your experience aligns with their quality assurance goals, especially in medical devices.
✨Tip Number 3
Showcase your leadership skills during interviews. Talk about how you've inspired teams and driven quality improvements. We love hearing about real-life examples that demonstrate your impact!
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we’re always looking for passionate individuals who want to make a difference in quality assurance.
We think you need these skills to ace Global Quality Assurance Manager
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 our mission at Vernacare!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to express your passion for quality assurance in medical devices and how you can make an impact at Vernacare. Don’t forget to mention specific examples of your leadership and continuous improvement initiatives.
Showcase Your Leadership Skills: As a leader, it’s crucial to demonstrate your ability to inspire and mentor teams. In your application, share stories that highlight your leadership style and how you've successfully driven quality culture in previous roles. We love seeing candidates who can lead from the front!
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’re considered for this exciting opportunity. Plus, it shows you’re keen on joining the Vernacare family!
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 management. 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 quality management systems. Brush up on your technical knowledge and be prepared to discuss specific challenges you've faced and how you overcame them using Six Sigma or Lean methodologies.
✨Demonstrate Cross-Functional Collaboration
Since this role involves working with various departments, think of examples where you successfully collaborated with teams like NPD, manufacturing, or regulatory affairs. Show that you understand the importance of teamwork in achieving quality goals.
