Job Description:

Quality Engineer (12-Month Contract)

Location: Witney, Oxfordshire

Salary: £33,000 - £60,000 per annum (Dependent on Experience)

Hours: Full-Time, 37.5 hours per week (Monday to Friday)

Contract Length: 12 Months

We are seeking a skilled and adaptable Quality Engineer to join a global medical device company based in Witney. This is a highly collaborative, cross-functional role where you will support a range of processes from R+D to clinical groups to transport and sterilisation.

We are looking for a professional who has interest in supporting Design Validation or Test Method Validation (TMV), who can make critical quality and compliance decisions during product development, validation, and testing. Acting as a Subject Matter Expert (SME), you will manage project activities to ensure our processes meet both business and customer needs flawlessly.

Role Details:

Location: Witney, Oxfordshire

Salary: £33,000 - £60,000 per annum Hours: Full-Time, 37.5 hours per week (Monday to Friday)

Contract Length: 12 Months

Key Responsibilities

• Validation & Compliance Decisions: Make definitive Quality and Compliance decisions on products throughout development, validation, processing, and testing phases.
• Cross-Functional Project Management: Project-manage cross-functional activities to agreed timelines, utilising appropriate risk management tools to prioritise efforts and safeguard quality.
• Relationship Management: Maintain successful, collaborative relationships with cross-functional departments, including R&D, Technical, Engineering, Operations, and Regulatory Affairs to achieve project milestones.
• QMS Monitoring & Improvement: Review, approve, and assess the impact of changes or corrections to documentation, processes, or systems to ensure effective and compliant QMS procedures.
• Audit & Expert Representation: Act as the Subject Matter Expert (SME) during audits, cross-functional meetings, and site/divisional level projects.
• Meticulous Record Keeping: Ensure all record completion strictly adheres to defined procedures and quality standards, securing and storing data appropriately.
• EHS & Ethics: Maintain safe working environments by supporting Environment, Health, and Safety (EHS) performance and ensuring all business behaviours align strictly with the corporate Code of Conduct.

What We Are Looking For

• Proven experience as a Quality Engineer with a dedicated focus on design validation or test method validation.
• Prior experience in the development and/or manufacture of regulated products, demonstrating a strong familiarity with cGMP and/or ISO Quality System requirements.
• Demonstrated ability to build and maintain relationships across multiple engineering and technical disciplines.
• Strong technical understanding of validation principles, statistics, and risk management tools.
• Secondary level education including English and Maths (or equivalent).
• Relevant Degree or equivalent qualification.
• Note: The wide salary band reflects our openness to considering both intermediate and senior-level engineers. Salary will be closely aligned with your specific depth of experience.

What's on Offer?

• Work-Life Balance: Standard 37.5-hour work week with a dependable Monday to Friday schedule.
• Onsite Perks & Benefits: * Onsite parking
• Electric vehicle charging stations
• Subsidised canteen
• Free Lavazza coffee machines

How to Apply

If you are a validation specialist who thrives in a collaborative, cross-functional environment and has experience navigating regulated QMS environments, we want to hear from you.

Randstad Business Support is acting as an Employment Business in relation to this vacancy.