At a Glance
- Tasks: Lead the Quality Assurance team in ensuring design assurance for cancer diagnostic products.
- Company: Leica Biosystems is a global leader in cancer diagnostics, dedicated to improving lives through innovative solutions.
- Benefits: Enjoy a dynamic work environment with opportunities for growth and development in a meaningful field.
- Why this job: Make a real impact in cancer diagnostics while collaborating with a diverse, global team.
- Qualifications: Experience in IVD medical device development and leadership skills are essential.
- Other info: This is an on-site role based in Newcastle-upon-Tyne, UK.
The predicted salary is between 48000 - 72000 £ per year.
Leica Biosystems\’ mission of \”Advancing Cancer Diagnostics, Improving Lives\” is at the heart of our corporate culture. We\’re a global leader in cancer diagnostics with the most comprehensive portfolio from biopsy to diagnosis. Our easy-to-use and consistently reliable offerings help improve workflow efficiency and diagnostic confidence. Our associates know that every moment matters when it comes to cancer diagnostics. When you come to work, you\’re helping develop solutions that enable accurate diagnoses to turn anxiety into answers. Join our diverse, global team of talented people, and be inspired to grow every day.
Leica Biosystems is proud to work alongside a community of six fellow Diagnostics Companies at Danaher. Together, we\’re working at the pace of change to improve patient lives with diagnostic tools that address the world\’s biggest health challenges.
The Manager, Quality Assurance (Design) for Leica Biosystems is responsible for design assurance and leadership within the QARC team to support the Newcastle site to deliver and sustain advance staining reagents and diagnostic assays in the clinical market. This role will oversee multiple project deliverables, as well as provide review and guidance for risk management, verification and validation activities related to the development projects and the sustainment of documentation under IVDR.
This position is part of the Quality Assurance & Regulatory Compliance department located in Newcastle-upon-Tyne, UK and will be an on-site role. At Leica Biosystems, our vision is to advance cancer diagnostics and improve lives.
You will be a part of the Quality Assurance team and report to the Director, QARC responsible for ensuring that the business has the infrastructure and skilled QARC competencies to meet or exceed requirements. If you thrive in a fast paced, leadership role and want to work to build a world-class Quality Assurance & Regulatory Compliance organization-read on.
In this role, you will have the opportunity to:
- Leadership and management responsibilities for QA professionals covering design assurance and QMS duties.
- Responsible for planning, organizing, and conducting duties related to design assurance.
- Manage business-critical new product development projects and external partnership programs, including ensuring that state-of-the-art requirements are maintained throughout the product lifecycle.
- Hire, develop, engage and retain highly capable Quality Officers and Specialists ensuring that each associate is meeting performance requirements and that each people leader role and critical position has an identified successor with a targeted and robust development plan.
- Participate in cross-functional teams at various phases of the development cycle as the Design Assurance representative. Collaborate globally and cross-functionally (e.g., Clinical Affairs, Business Development, Regulatory Assurance, Research & Development, Product/Program Management) to achieve project goals and meet timelines.
- Collaborate with Regulatory Affairs to Input into the regulatory strategy and plans for clearance/approval of Leica Biosystems technologies intended for cancer diagnostics in the anatomic pathology, IVD and Companion Diagnostics markets, including providing input into 510(k), PMA and companion diagnostic submissions.
- Use Danaher Business System (DBS) tools on a regular basis to continually improve the QA design assurance function.
The essential requirements of the job include:
- Working knowledge of design controls for regulated products.
- Experience in IVD medical device new product development and design controls.
- Prior management experience or demonstration of leadership skills.
- Extensive knowledge of international IVD medical device quality systems including but not limited to 21 CFR 820, MDSAP and ISO 13485.
It would be a plus if you also possess previous experience in:
- IVD medical device regulatory affairs experience a distinct advantage.
Join our winning team today. Together, we\’ll accelerate the real-life impact of tomorrow\’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.
For more information, visit .
At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.
Manager, Quality Assurance (Design) employer: Leica Biosystems
Contact Detail:
Leica Biosystems Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Manager, Quality Assurance (Design)
✨Tip Number 1
Familiarise yourself with the latest trends and regulations in IVD medical devices. Understanding the current landscape will not only help you in interviews but also demonstrate your commitment to staying updated in a rapidly evolving field.
✨Tip Number 2
Network with professionals in the Quality Assurance and Regulatory Compliance sectors. Attend industry conferences or webinars to connect with potential colleagues and learn more about the company culture at Leica Biosystems.
✨Tip Number 3
Prepare to discuss your leadership experiences in detail. Be ready to share specific examples of how you've successfully managed teams and projects, particularly in high-pressure environments, as this role requires strong management skills.
✨Tip Number 4
Research Leica Biosystems' products and their impact on cancer diagnostics. Being knowledgeable about their offerings will allow you to speak confidently about how your skills can contribute to their mission during the interview process.
We think you need these skills to ace Manager, Quality Assurance (Design)
Some tips for your application 🫡
Understand the Role: Before applying, make sure you fully understand the responsibilities and requirements of the Manager, Quality Assurance (Design) position. Familiarise yourself with Leica Biosystems' mission and how your skills align with their goals.
Tailor Your CV: Customise your CV to highlight relevant experience in quality assurance, design controls, and IVD medical device development. Emphasise any leadership roles you've held and specific projects that demonstrate your ability to manage teams and deliver results.
Craft a Compelling Cover Letter: Write a cover letter that not only outlines your qualifications but also expresses your passion for advancing cancer diagnostics. Mention how your background aligns with the company's mission and how you can contribute to their success.
Highlight Relevant Skills: In your application, be sure to showcase your knowledge of international IVD medical device quality systems and any experience with regulatory affairs. Use specific examples to illustrate your expertise in design assurance and project management.
How to prepare for a job interview at Leica Biosystems
✨Understand the Company Mission
Familiarise yourself with Leica Biosystems' mission of 'Advancing Cancer Diagnostics, Improving Lives'. Be prepared to discuss how your values align with this mission and how you can contribute to their goals.
✨Showcase Your Leadership Experience
As a Manager, Quality Assurance, you'll need to demonstrate your leadership skills. Prepare examples of how you've successfully led teams, managed projects, and developed talent in previous roles.
✨Highlight Relevant Technical Knowledge
Make sure to brush up on your knowledge of design controls for regulated products and IVD medical device quality systems. Be ready to discuss specific regulations like 21 CFR 820 and ISO 13485, as these will be crucial in your role.
✨Prepare for Cross-Functional Collaboration Questions
Since the role involves working with various departments, think of examples where you've successfully collaborated across functions. Be ready to explain how you can facilitate communication and teamwork in a diverse environment.