Lead Verification and Validation Engineer

JR United Kingdom; Slough; Hybrid; GBP 100,000 - 125,000; Full time

Job summary

A leading company in the medical device sector is seeking a Lead Verification and Validation Engineer for a 12-month contract. The role involves overseeing design outputs, conducting verification testing, and ensuring compliance with regulatory standards. With a flexible working model and a focus on innovation, this position offers an exciting opportunity to be part of a groundbreaking project.

Qualifications

• Experience in design verification and validation processes in medical devices or pharmaceuticals.
• Strong analytical skills and attention to detail.
• Ability to lead cross-departmental collaboration.

Responsibilities

• Lead oversight of the completion of design outputs and labelling.
• Manage design verification and validation processes.
• Coordinate clinical trial documentation with CROs.

Skills

Oversight of design outputs

Design reviews

Design verification testing

Regulatory compliance

Job description

Lead Verification and Validation Engineer, slough

Client:

RBW Consulting

Location:

slough, United Kingdom

Job Category:

Other

Virtual job fairs

-

EU work permit required:

Yes

Job Views:

5

Posted:

31.05.2025

Expiry Date:

15.07.2025

Job Description:

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.

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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

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• 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.

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Created on 31/05/2025 by JR United Kingdom