At a Glance
- 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 with software as a medical device.
The predicted salary is between 60000 - 75000 € 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).
Engineering Quality Specialist (f/m/d) in London employer: SciPro
As a fast-growing, venture-backed technology company in the healthcare sector, we pride ourselves on fostering a dynamic and innovative work culture that empowers our employees to thrive. With a clear pathway for career advancement, including opportunities to evolve into roles such as Clinical Safety Officer, we offer a supportive environment where your contributions directly impact patient safety and product excellence. Located in London with a hybrid working model, we provide a flexible work-life balance while ensuring you are part of a collaborative team dedicated to making a meaningful difference in healthcare.
StudySmarter Expert Advice🤫
We think this is how you could land Engineering Quality Specialist (f/m/d) in London
✨Tip Number 1
Network like a pro! Reach out to people in the healthcare tech space, especially those who work at companies you're interested in. A friendly chat can open doors and give you insider info that could help you stand out.
✨Tip Number 2
Prepare for interviews by diving deep into the company’s products and values. Show them you’re not just another candidate; you’re genuinely excited about their mission and how you can contribute to their growth.
✨Tip Number 3
Don’t underestimate the power of follow-ups! After an interview, drop a quick thank-you email. It shows your enthusiasm and keeps you fresh in their minds as they make decisions.
✨Tip Number 4
Apply through our website! We’ve got loads of resources to help you ace your application and connect with the right people. Plus, it shows you’re serious about joining our team!
We think you need these skills to ace Engineering Quality Specialist (f/m/d) in London
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Engineering Quality Specialist role. Highlight your experience with Quality Management Systems and any relevant regulatory compliance work. We want to see how your skills align with our needs!
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you're passionate about quality in healthcare technology. Share specific examples of how you've ensured compliance and improved processes in previous roles.
Showcase Your Hands-On Experience:We love candidates who can combine strategic oversight with hands-on execution. Be sure to mention any direct experience you have with audits, inspections, or maintaining certifications. This will show us you’re ready to hit the ground running!
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 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 in the context of medical devices. 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 software as a medical device (SaMD) settings.
✨Be Ready for Scenario Questions
Expect questions that put you in hypothetical situations related to audit readiness and regulatory compliance. Think through your thought process and decision-making strategies to demonstrate your hands-on execution skills.
✨Highlight Cross-Functional Collaboration
This role requires working closely with various teams. Prepare to discuss how you’ve successfully translated regulatory requirements into actionable business decisions while collaborating with product, engineering, and operations teams.
