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Device Testing Consultant

Polytec Personnel Ltd
Posted a day ago, valid for a day
Location

Ickleton, Cambridgeshire CB10, England

Salary

£40,000 - £48,000 per annum

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Contract type

Full Time

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Sonic Summary

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  • Location: Cambridge (CB10), this is a permanent position with hours from 9am to 5:30pm, finishing at 5pm on Fridays.
  • The role offers a competitive salary and requires a minimum of 3 years of experience in regulated lab environments such as medical devices or pharmaceuticals.
  • The Device Testing Consultant will lead testing efforts, develop and validate test methods, and ensure compliance with health and safety standards.
  • Candidates should possess strong knowledge of ISO standards and be skilled in preparing technical documentation and statistical analysis.
  • The position also involves mentoring junior staff, engaging with clients, and contributing to business development efforts.

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!

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By applying, a CV-Library account will be created for you. CV-Library's Terms & Conditions and Privacy Policy will apply.