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Quality Engineer

Clinical Professionals Limited

Cambridgeshire and Peterborough

On-site

Full time

12 days ago

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Job summary

An established industry player is seeking a skilled Quality Engineer to join their Device Development Centre. This role involves working across the full product life cycle, collaborating with various teams to ensure compliance with medical device regulations. The ideal candidate will have a strong background in ISO standards and risk management, along with excellent communication skills. This is an exciting opportunity for professionals who are detail-oriented and passionate about quality assurance in medical devices. Join a forward-thinking company and contribute to the development of innovative healthcare solutions.

Qualifications

  • Experience working with ISO standards and medical device regulations.
  • Strong communication and interpersonal skills are essential.

Responsibilities

  • Work on the full product life cycle in a cross-functional team.
  • Ensure compliance with medical device regulations and quality standards.

Skills

ISO 13485
ISO 14971
21 CFR 820
Human Factors Engineering
Excellent communication skills
Attention to detail
Ability to work independently
Proficiency in computer software

Education

Relevant Degree or Higher Education Qualification

Job description

Reference Number: JO-2411-543881
Quality Engineer
Rate: Negotiable
Job Type: Contract
Location: Cambridge

Quality Engineer – Medical Devices

£21.62 – 12 month Contract

Cambridge

We are looking for an experienced Quality Engineer to join the team of an established Device Development Centre. The role will entail working on the full product life cycle, cross functional with the various teams and stakeholders involved.

Experience
  1. Relevant Degree or Higher Education Qualification
  2. History of working in accordance with the requirements of ISO 13485, ISO 14971, 21 CFR 820, 21 CFR 4, and the EU Medical Devices Regulation.
  3. Experience in design controls and risk management for combination products.
  4. Familiar with Human Factors Engineering – Usability Engineering.
  5. Familiar with device assembling manufacturing processes.
Technical Skills Requirements
  1. Working knowledge of ISO 9001, ISO 13485, ISO 14971, 21 CFR 820, 21 CFR 4, and the EU Medical Devices Regulation.
  2. Familiarity with EN 62366, EN 60601, and EN 62304.
  3. Able to learn and apply established procedures in a reliable and consistent manner.
  4. Capable of working independently with minimal supervision.
  5. High level of attention to technical details and accuracy.
  6. Able to prioritize multiple responsibilities and to work on multiple tasks simultaneously.
  7. Able to work collaboratively in cross functional teams.
  8. Excellent communication (e.g., oral, written, presentation) and interpersonal relationship skills.
  9. Proficiency in general computer software such as word processing, spreadsheets, presentations.
  10. Understand Good Manufacturing Practices (GMP).
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