At a Glance
- 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 Β£ 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 Bristol employer: Hartmann Young
Contact Detail:
Hartmann Young Recruiting Team
StudySmarter Expert Advice π€«
We think this is how you could land Senior Director Quality Assurance - MedTech (UK) in Bristol
β¨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.
β¨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.
β¨Tip Number 3
Donβt 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.
β¨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, especially in a fast-paced environment.
We think you need these skills to ace Senior Director Quality Assurance - MedTech (UK) in Bristol
Some tips for your application π«‘
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 leadership position, make sure to highlight your people-focused, collaborative approach. Weβre looking for someone who can mentor and develop a team, so share any relevant experiences that demonstrate your leadership style.
Apply Through Our Website: Donβt forget to apply through our website! Itβs the best way for us to receive your application and ensure it gets the attention it deserves. We canβt wait to see what you bring to the table!
How to prepare for a job interview at Hartmann Young
β¨Know Your Quality Standards
Make sure youβre 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.
β¨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, people-focused approach and how it has fostered collaboration and a positive culture in your previous roles.
β¨Demonstrate Your Strategic Vision
This role requires setting and executing a global quality strategy. Think about how you would approach this and be ready to discuss your vision for the quality function in a rapidly scaling organisation. Show that you can align quality with business growth and operational needs.
β¨Prepare for Cross-Functional Collaboration
Youβll need to act as a trusted partner across various departments. Prepare to discuss how you've successfully collaborated with Operations, R&D, and Regulatory teams in the past. Share specific instances where your input made a significant impact on product quality or operational efficiency.