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Location: Cambridge (CB10) Duration: Permanent Hours: 9am until 5:30pm (Monday to Friday) 5pm finish Friday Salary: Competitive Job Reference: 35721 We are seeking an experienced Device Testing Consultant to support a range of medical and drug delivery device projects for our south Cambs based client. This is a hands-on, lab-based role involving planning and leading test activities, mentoring junior staff and engaging with clients. Responsibilities Lead device testing efforts across RandD, design verification and post-market phases Develop and validate test methods, equipment and software Ensure compliance with health, safety and quality standards (e.g., ISO 13485, cGxP) Prepare technical documentation including test plans, protocols, reports and validation records Provide expert training and statistical analysis support Represent the team at client meetings and industry events Contribute to proposal writing and business development Requirements Essential: 3+ years in regulated lab environments (e.g., medical devices, pharmaceuticals) Strong knowledge of ISO standards, cGxP, ALCOA+ and health and safety practices Skilled in test method development and equipment/software validation (IQ/OQ/PQ) Experience preparing technical documentation and statistical data analysis (Minitab or similar) Excellent communication and organizational skills Passionate about medical technology and continuous improvement Practical, methodical and detail-oriented Strong interpersonal and team leadership abilities Adaptable, reliable and solution-focused Desirable: Background in consulting or client-facing technical roles. Experience with design verification and third-party supplier engagement. Familiarity with risk/COSHH assessments and technical writing for diverse audiences. Please contact us as soon as possible for more details or apply below.
Date Posted: 30 May 2025
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