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Senior Associate Device Engineer

Cpl Life Sciences·Cambridge (East Anglia)On-site12-Month ContractSenior
£21 / hourestimated
Vox Summary
  • Role Overview: Support development and evaluation of drug delivery devices within a multidisciplinary engineering team.
  • Key Responsibilities: Design and execute testing, develop test methods, support verification, analyze data, contribute to risk management, and ensure quality procedures.
  • Requirements: Degree or HND in Mechanical/Biomedical Engineering or related, experience in medical devices, knowledge of device testing, ISO 13485, FMEA, and CAD software.
  • Conditions & Benefits: 12-month contract, £21.00 per hour PAYE, 37 hours per week, Cambridge location.
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Job description

Senior Associate Device Engineer Cambridge 12-Month Contract £21.00 per hour PAYE (37 hours per week) We're recruiting for a Senior Associate Device Engineer to support the development and evaluation of innovative drug delivery devices within a multidisciplinary engineering team. This is an excellent opportunity for an engineer with experience in medical devices, drug delivery systems or combination products to work on the testing, analysis and verification of devices such as syringes and cartridges throughout the product development lifecycle. Key responsibilities: • Design and execute mechanical and functional testing of drug delivery devices. • Develop test methods, experimental rigs and laboratory test setups. • Support design verification and validation activities. • Analyse experimental data using statistical techniques and Design of Experiments (DOE). • Contribute to risk management activities, including FMEA. • Support design control documentation and technical reporting. • Work closely with design, quality, regulatory, human factors and formulation teams. • Ensure laboratory activities are carried out in accordance with ISO 13485 and established quality procedures. About you: • Degree or HND in Mechanical Engineering, Biomedical Engineering or a related Engineering/Science discipline. • Experience within the medical device, pharmaceutical or drug delivery sector. • Knowledge of design verification, device testing and analytical test methods. • Familiarity with ISO 13485, design controls and risk management (FMEA). • Experience using CAD software (Creo preferred). • Strong analytical and problem-solving skills with a hands-on approach to engineering. If you're looking for your next contract opportunity within a collaborative R&D environment and have experience developing or testing regulated medical devices, we'd love to hear from you. Apply today with your CV, or get in touch for more information.

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Original source
reed.co.uk
Posted
Jul 14, 2026 · true date
Last verified
2 hours ago
Quality score
35/100
Salary stated0
Company identified0
applyUrl0
postedAt15
Complete description20

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