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