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Lead Verification and Validation Engineer

Lead Verification and Validation Engineer

Hybrid

London, United kingdom

£ 62 /hour

Freelance

12-05-2025

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Expired

Job Specifications

Lead Verification & Validation Engineer | 12 month contract | £350-500 per day | Outside IR35 | London | Immediate start

One of my long-standing clients is looking for a V&V engineer as they transfer into manufacturing, ideally with a background in combination devices/pharmaceutical products.

They're based in London, but have a flexible working model. You'll be working closely with various heads of department to engender a collaborative and productive working environment.

They're true innovators into a critical area of unmet need, with a genuinely ground-breaking product.

Job overview:
Oversight of completion of design outputs, including technical drawings, product and component specifications
Oversight of the completion of labelling and packaging design in alignment with the relevant medical device and pharma labelling standards and regulations
To lead the design reviews for the device, ensuring the product design is evaluated against requirements detailed within the TRS and URS
To lead the design verification testing of the device and associated labelling and packaging.
Coordinate the supply of raw materials for the manufacture of DV samples
Ensure test methods are documented, validated and staff are trained (training is recorded)
Develop the design verification protocol, including traceability to the TRS and test reports
Coordinate internal and external testing in accordance with the protocol
Analyse test data and prepare a design verification report
To lead the design validation of the device, including Clinical trials

As above for design verification, plus:
Liaison with the CRO, including the coordination of all documentation and evidence required for the clinical trial
Maintain the design history file in accordance with 21 CFR part 820 requirements
Manage product change control, in accordance with the relevant CLCC procedures
Maintain the Device Master Record in accordance with 21 CFR part 820 requirements

Regulatory
Collate the Technical File in accordance with the relevant regulations (could be UK, EU and / or US)

Please apply right away to be considered for this great opportunity.

About the Company

RBW Consulting is a proudly B Corp certified life sciences recruitment & search consultancy with purpose, delivered through what we call Human Intelligence. We help life sciences businesses change the world by giving them the people, insight & networks to innovate and scale. We are proud of our role in helping companies deliver better health and wellbeing outcomes for patients We give back by playing an active role in funding initiatives that change lives We've created a culture rooted in support, transparency and mutua... Know more