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- Tasks: Own the Quality Management System and ensure compliance in a fast-paced healthcare tech environment.
- Company: Join a rapidly growing, venture-backed tech company transforming healthcare.
- Benefits: Hybrid working model, competitive salary, and opportunities for career advancement.
- Other info: Clear pathway to grow into a Clinical Safety Officer role.
- Why this job: Make a real impact on healthcare innovation while ensuring quality and safety.
- Qualifications: Experience in regulated environments, especially software as a medical device.
The predicted salary is between 50000 - 65000 £ per year.
We’re working with a fast-growing, venture-backed technology company operating within the healthcare space. Following recent funding, the company is now entering a key growth phase as they scale their product and expand adoption.
Sitting at the intersection of product, engineering, and operations, you will ensure regulatory requirements are met while enabling the company to move quickly and scale effectively. You will take full ownership of the Quality Management System (QMS), oversee medical device compliance, and act as the internal lead for ISO standards. This role combines strategic oversight with hands-on execution and will be critical in building scalable, audit-ready processes.
There is also a clear pathway to take on (or grow into) a Clinical Safety Officer (CSO) position, contributing to clinical risk management and safety governance as the product evolves.
- Own and evolve the company’s Quality Management System (QMS)
- Ensure ongoing compliance as the product develops (features, integrations, deployments)
- Maintain audit readiness across documentation, policies, and controls
- Lead preparation for audits, inspections, and certifications
- Maintain relevant certifications and regulatory approvals
- Support clinical safety processes, including risk assessments and governance frameworks
- Act as a cross-functional partner, translating regulatory requirements into practical business decisions
Experience working within a regulated environment, ideally software as a medical device (SaMD). London-based, with a hybrid working model (3 days in-office).
Quality Specialist Project in London employer: SciPro
Contact Detail:
SciPro Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Quality Specialist Project in London
✨Tip Number 1
Network like a pro! Reach out to people in the healthcare tech space, especially those who work with quality management systems. 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 ISO standards and regulatory requirements. We want you to be the go-to person for compliance discussions, so show off your knowledge and how it can help the company scale effectively.
✨Tip Number 3
Don’t just apply anywhere; focus on companies that align with your values and career goals. Use our website to find roles that excite you, and tailor your approach to each one. It’s all about finding the right fit!
✨Tip Number 4
Follow up after interviews! A quick thank-you email can keep you top of mind and show your enthusiasm for the role. Plus, it’s a great chance to reiterate why you’re the perfect fit for their Quality Management System.
We think you need these skills to ace Quality Specialist Project in London
Some tips for your application 🫡
Tailor Your CV: Make sure your CV reflects the skills and experiences that align with the Quality Specialist Project role. Highlight any experience you have in regulatory environments, especially in healthcare or software as a medical device (SaMD).
Craft a Compelling Cover Letter: Use your cover letter to tell us why you're passionate about quality management and how your background makes you a great fit for our team. Be specific about your achievements and how they relate to the responsibilities outlined in the job description.
Showcase Your Attention to Detail: As a Quality Specialist, attention to detail is key. Make sure your application is free from typos and errors. This not only shows your commitment but also reflects the quality standards we uphold at StudySmarter.
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 the role. Plus, it gives you a chance to explore more about our company culture and values!
How to prepare for a job interview at SciPro
✨Know Your QMS Inside Out
Make sure you’re well-versed in Quality Management Systems, especially how they apply to the healthcare and medical device sectors. Brush up on ISO standards and be ready to discuss how you’ve implemented or improved QMS in previous roles.
✨Showcase Your Compliance Experience
Prepare examples of how you've ensured compliance in a regulated environment. Be specific about the challenges you faced and how you overcame them, particularly in relation to software as a medical device (SaMD).
✨Be Ready for Scenario Questions
Expect questions that put you in hypothetical situations regarding audits, inspections, or compliance issues. Think through your thought process and decision-making strategies in advance so you can articulate them clearly.
✨Highlight Cross-Functional Collaboration
This role requires working with various teams, so be prepared to discuss how you’ve successfully collaborated across departments. Share specific instances where you translated regulatory requirements into actionable business decisions.