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Device Project Lead

SRG
Posted 3 days ago, valid for a month
Location

Cambridge, Cambridgeshire CB21NT, England

Salary

£45,000 - £54,000 per annum

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Contract type

Part Time

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Sonic Summary

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  • The Device Project Lead position is located in Cambridge with a hybrid work pattern and is a 6-month contract role.
  • The role offers a pay rate of up to £380 per day via Umbrella.
  • Candidates should have a university degree in a relevant subject and at least 3 years of work experience in medical devices or combination product development.
  • Key responsibilities include project leadership, development oversight, and management of cross-functional device project teams.
  • The ideal candidate must possess knowledge of GMP, international device regulations, and have strong communication skills in a diverse setting.

Job Title - Device Project Lead

Location - Cambridge (hybrid work pattern)

Contract - 6 months

Pay - Up to 380 per day via Umbrella

SRG are working with a global leading pharmaceutical company that are seeking a Device Project Lead to join their busy team.

A growing pipeline of medical device and drug/device combination projects. To meet our ambitious future portfolio needs, we are seeking a Device Project Lead in the development of medical and drug delivery devices. By successfully leading the development of the medical devices/combination products, you will help to launch commercially competitive products that will increase access for our patients.

Key responsibilities:

  • Project leadership (planning, co-ordination, specifications, risk management, documentation, design transfer etc.)
  • Development oversight (market research; user research; concept generation, development and analysis; detail design (e.g. including 3D CAD and engineering drawings); ergonomics and usability (including HF/UE documentation); design reviews).
  • creation and management of Design History Files and associated documentation for selected combination products in accordance with the annual plan and objectives, and relevant standards and guidances e.g. ISO13485, 21 CFR Part 820.30, 21 CFR 3.2(e).
  • Lead, represent, and manage cross-functional device project teams.
  • Management of activities in accordance with project strategies, budget, timelines, regulatory, quality, and professional standards.
  • Enabling operational excellence in compliance with the current and anticipated professional trends.
  • Performing activities in compliance with Good Manufacturing Practice
  • Ensuring inspection readiness

Basic Qualifications:

  • University degree in relevant subject (mechanical engineering, product design, physics etc.) or other equivalent degree.
  • Knowledge of GMP and international device regulations.
  • Ability to communicate and collaborate effectively in a highly international and diverse setting
  • Track record of goal-driven behaviour, problem solving, ability to make pragmatic decisions, readiness for new challenges
  • Work experience in medical devices/combination product development.
  • Knowledge of regulatory/QA requirements for medical devices/combination products; and
  • Digital excellence and automation of documentation


Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.

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