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- Tasks: Lead the evolution of quality systems in a rapidly scaling MedTech company.
- Company: Join a pioneering MedTech firm at the forefront of Neurotechnology.
- Benefits: Competitive salary, leadership role, and global impact across U.S. and Europe.
- Why this job: Shape the future of quality in a dynamic, fast-paced environment.
- Qualifications: 10+ years in MedTech quality with leadership experience required.
- Other info: On-site role with opportunities for professional growth and development.
The predicted salary is between 72000 - 108000 £ per year.
We are partnered with a rapidly scaling MedTech company at the forefront of Neurotechnology to appoint a Senior Director of Quality. This newly created role will lead the evolution of the Quality function as the organisation scales, with a focus on building robust, inspection-ready systems, developing a high-performing team, and embedding quality as a true business partner. Reporting to the COO, this is a senior, on-site leadership role with global scope across the U.S. and Europe.
Key Responsibilities
- Set and execute the global quality strategy to support business growth and increasing organisational maturity.
- Own and continuously improve the Quality Management System in line with FDA, ISO 13485, and EU MDR requirements.
- Ensure sustained inspection readiness while maintaining practical, scalable quality processes.
- Lead, mentor, and develop a growing Quality organisation, including upskilling middle management.
- Oversee quality operations, quality programmes, and supplier/manufacturing quality activities.
- Act as a trusted, cross-functional partner to Operations, R&D, Regulatory, and senior leadership.
- Champion a pragmatic quality culture that supports the business rather than constrains it.
Requirements
- Significant experience in medical device quality within regulated environments (FDA and EU).
- Prior experience at Head of Quality, Senior Director, or equivalent senior leadership level.
- Proven track record of scaling quality systems and teams in growing MedTech organisations.
- Strong background in product quality, quality systems, and operational quality (not regulatory-led).
- Experience with complex or active medical devices; Neuro or energy-based technologies preferred.
- Hands-on, people-focused leader with a collaborative, low-ego leadership style.
- Comfortable operating on site in a fast-paced, evolving environment (no hybrid / no visa sponsorship).
- Class II Medical Device experience.
- 10 years experience in MedTech industry and experiencing scale with a startup.
- Science or Engineering degree.
If you are interested in learning more, please apply using the link or reach out to me directly at: raj.tamana@hartmannyoung.com
Senior Director Quality Assurance - MedTech (UK) in Birmingham employer: Hartmann Young
Contact Detail:
Hartmann Young Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Director Quality Assurance - MedTech (UK) in Birmingham
✨Tip Number 1
Network like a pro! Reach out to your connections in the MedTech industry, especially those who have experience in quality assurance. A friendly chat can lead to insider info about job openings or even referrals.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of FDA and ISO 13485 standards. We want you to showcase your expertise in quality management systems, so be ready to discuss how you've implemented these in past roles.
✨Tip Number 3
Don’t just apply; engage! When you submit your application through our website, follow up with a quick email to express your enthusiasm. It shows initiative and keeps you on their radar.
✨Tip Number 4
Showcase your leadership style! In interviews, share examples of how you've developed teams and fostered a quality culture. We want to see that you can lead with a collaborative approach while driving results.
We think you need these skills to ace Senior Director Quality Assurance - MedTech (UK) in Birmingham
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Senior Director Quality Assurance role. Highlight your experience in medical device quality and any leadership roles you've held. We want to see how your background aligns with 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. Share specific examples of how you've built quality systems and led teams in the past. We love a good story that showcases your skills!
Showcase Your Achievements: When filling out your application, don’t just list your responsibilities—show us your achievements! Quantify your successes where possible, like improvements in inspection readiness or team performance. Numbers speak volumes!
Apply Through Our Website: We encourage you to apply through our website for a smoother process. It helps us keep track of applications and ensures you don’t miss any important updates. Plus, it’s super easy to do!
How to prepare for a job interview at Hartmann Young
✨Know Your Quality Standards
Make sure you’re well-versed in FDA, ISO 13485, and EU MDR requirements. Brush up on how these standards apply to the MedTech industry, especially in relation to neurotechnology. Being able to discuss specific examples of how you've implemented these standards in previous roles will show your expertise.
✨Showcase Your Leadership Style
As a Senior Director, your leadership style is crucial. Be prepared to share examples of how you've led teams in the past, particularly in scaling quality systems. Highlight your hands-on approach and collaborative mindset, as this aligns with the company’s culture.
✨Demonstrate Your Strategic Thinking
Think about how you would set and execute a global quality strategy. Be ready to discuss your vision for building robust, inspection-ready systems and how you would ensure sustained inspection readiness while supporting business growth. This will show that you can think big picture.
✨Prepare for Cross-Functional Collaboration
This role requires acting as a trusted partner across various functions. Prepare to discuss how you've successfully collaborated with Operations, R&D, and Regulatory teams in the past. Share specific instances where your quality initiatives positively impacted other departments.
