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Greenfield Medical Device Development Programme
Major New Product Introduction
This is an opportunity to join a medical device organisation at a truly pivotal stage in its growth. Having recently secured substantial funding, the company is now preparing to launch an innovative new product and is building out the core team that will take it from concept through to global commercialisation.
They are seeking an experienced Design Assurance / Design Quality Lead to take ownership of the design quality strategy for this next-generation medical device. It is a chance to build and shape quality frameworks from the ground up while working on a product that will have a real-world impact on patient outcomes.
What Makes This Opportunity Stand Out?
Long-Term Opportunity with potential to transition into a permanent role
Major New Product Introduction from concept through to global launch
High-Impact Medical Device addressing real-world healthcare needs
Collaborative, highly skilled team environment
What You’ll Be Doing
Leading design assurance activities across the full product development lifecycle
Owning Design Controls and ensuring compliance with medical device regulations and standards
Establishing and developing SOPs, quality processes, and documentation frameworks from scratch
Building and maintaining Design History Files (DHF) and Device Master Records (DMR)
Driving traceability across requirements, risk management, verification and validation
Supporting design reviews, risk management plans, and V&V activities
Collaborating closely with regulatory teams to support global submissions
Ensuring successful design transfer into manufacturing environments
Acting as the quality representative across cross-functional program teams
What You’ll Need
8–10 years’ hands‑on experience in medical device quality or design assurance xcfaprz
Proven experience delivering New Product Introductions (NPI) from concept to commercialisation
Strong knowledge of medical device quality systems and regulatory frameworks
Hands‑on experience building processes, documentation, and quality frameworks – not just reviewing them
Experience working with combination devices, wearable devices, or CGM technologies
Expertise in design controls, risk management, and verification & validation processes
A proactive mindset with the confidence to lead quality initiatives within a fast-moving product environment
Contact Declan Ferrao on or send your CV to
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Compétences linguistiques
- English
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