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- Tasks: Lead the evolution of quality systems in a fast-growing MedTech company.
- Company: Rapidly scaling 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 innovative medical technology.
- Qualifications: 10+ years in MedTech quality, strong leadership, and hands-on experience.
- Other info: On-site role in a dynamic environment with significant growth opportunities.
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 London 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 London
✨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 a referral.
✨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 wait for job postings! Be proactive and reach out to companies directly, especially those in the Neurotechnology space. Express your interest in their work and ask if they have any upcoming opportunities.
✨Tip Number 4
When applying, make sure to highlight your leadership style and experience in scaling teams. We want to see how you can build a high-performing quality organisation that aligns with business goals, so let that shine through!
We think you need these skills to ace Senior Director Quality Assurance - MedTech (UK) in London
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 Leadership Style: Since this is a senior role, it's important to convey your leadership style. We’re looking for someone who is hands-on and people-focused. Make sure to include examples of how you've mentored teams and fostered a collaborative environment.
Apply Through Our Website: Don't forget to apply through our website! It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it shows you’re serious about joining our team!
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. This will show that you’re not just familiar with quality assurance but that you can lead the charge in building robust systems.
✨Showcase Your Leadership Style
Prepare to discuss your hands-on, people-focused leadership approach. Think of examples where you've successfully mentored teams or developed middle management. Highlighting your collaborative style will resonate well, especially since they’re looking for a low-ego leader who can thrive in a fast-paced environment.
✨Demonstrate Your Strategic Vision
Be ready to articulate your vision for scaling quality systems in a growing organisation. Discuss specific strategies you’ve implemented in the past that align with business growth and maturity. This will help them see you as a true business partner rather than just a quality gatekeeper.
✨Prepare for Cross-Functional Collaboration
Think about how you’ve worked with Operations, R&D, and Regulatory teams in previous roles. Prepare anecdotes that illustrate your ability to act as a trusted partner across functions. This will be crucial, as they want someone who can champion a pragmatic quality culture that supports the business.
