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Job verified 15 hours ago

Project Quality Lead

SDL Solutions Limited·Cambridge (East Anglia)Hybrid12 month ContractLead
Salary not stated
Vox Summary
  • Role Responsibilities: Coordinate quality activities throughout the product lifecycle, support validation, lead design reviews, and collaborate with teams and suppliers.
  • Key Requirements: Degree in Life Sciences, Engineering, or related field; experience in product development quality support; knowledge of ISO, GMP, Medical Device regulations; team coordination skills.
  • Conditions & Benefits: 37.5-hour work week, primarily site-based with hybrid arrangements, 12-month contract, eligible to work in the UK.
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Job description

We are seeking an experienced Project Quality Lead to join the Quality team at our client's site. This role is responsible for coordinating quality activities throughout the product lifecycle, ensuring compliance with Quality Management System (QMS) requirements, supporting risk management processes, and collaborating closely with Project Leads, Product Development teams, and suppliers. Key Responsibilities • Coordinate quality activities across the product lifecycle. • Support product validation, root cause investigations, and quality-related operational activities. • Lead and approve design reviews and risk management activities. • Review and approve product, process, and project documentation to ensure compliance with QMS requirements. • Support the implementation and continuous improvement of quality processes and procedures. • Provide guidance on design controls, risk management, and quality best practices. • Assist in the creation and review of project quality documentation. • Collaborate with internal teams and external suppliers to ensure quality objectives are achieved. Requirements • Bachelor's or Master's degree in Life Sciences, Engineering, or a related discipline. • Experience providing Quality Management support within product development environments, ideally in the pharmaceutical, biopharmaceutical, or medical device sectors. • Knowledge of quality standards and regulatory requirements, including ISO, GMP, and/or Medical Device regulations. • Previous experience leading or coordinating teams. • Strong communication, organisational, and stakeholder management skills. • Analytical mindset with the ability to manage priorities and support both short and long-term objectives. EligibilityApplicants must have the right to work in the UK. Working Conditions • 37.5-hour working week. • Primarily site-based, with hybrid working arrangements available by agreement. Commutable from: - Welwyn, WGC, Hatfield, St Albans, Watford, Harpenden, Borehamwood, Hitchin, Stevenage, Potters Bar, Letchworth, Baldock, Royston, Ware, Hertford, Enfield, Hoddesdon, Broxbourne, Luton, Hemel Hempstead, Biggleswade, Saffron Walden, Haverhill, Braintree, Ely, Newmarket, St Neots, St Ives, Milton Keynes, Bedfordshire, Buckinghamshire, Essex, Norfolk, Suffolk, Cambridge, London Project Quality Lead - 12 month Contract

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Original source
reed.co.uk
Posted
Jun 12, 2026 · true date
Last verified
15 hours ago
Quality score
35/100
Salary stated0
Company identified0
applyUrl0
postedAt15
Complete description20

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