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Device Development Engineer

2 months ago

Cambridge, Cambridgeshire, United Kingdom Russell Tobin Full time
Job Description

Job Title: Quality Engineer

Company: Russell Tobin

Location: Cambridge (Hybrid with 2-3 days onsite per week)

Job Type: Contract

Duration: 12 months

Salary: up to £21.62 PAYE and £24 per hour Umbrella

Responsibilities:

  • Lead design control and risk management activities for combination product development programs, ensuring deliverables are appropriately authored, approved, and maintained to support clinical trials and commercial licensures.
  • Support and facilitation of effective risk management activities at external design companies and manufacturing facilities related to assigned projects.
  • Ensure combination product development activities are compliant with quality and regulatory standards, both internal and external.
  • Provide input and support to design validation including, but not limited to, human factors engineering assessments.
  • Support the assessment of external design companies and suppliers for capability of quality systems, facilities, and procedures to support device development and supply.
  • Support device design and manufacturing investigations from devices used in clinical trials and commercial manufacture.
  • Support the generation of all regulatory submission data and content for assigned device projects.
  • Support internal and external audits of the DCoE Quality Management System.

Requirements:

  • BSc in an appropriate science and engineering discipline with a minimum of 2 years of relevant experience in the pharmaceutical combination product and/or device industries OR MSc in an appropriate science and engineering discipline with a minimum of 2 years of relevant experience in the pharmaceutical combination product and/or device industries OR PhD in an appropriate science and engineering discipline.
  • 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.
  • Experience in design controls and risk management for combination products.
  • Familiarity with Human Factors Engineering - Usability Engineering.
  • Familiarity with device assembling manufacturing processes.

Technical Skills:

  • Working knowledge of ISO 9001, ISO 13485, ISO 14971, 21 CFR 820, 21 CFR 4, and the EU Medical Devices Regulation.
  • Familiarity with EN 62366, EN 60601, and EN 62304.
  • Able to prioritize multiple responsibilities and to work on multiple tasks simultaneously.
  • Able to work collaboratively in cross-functional teams.
  • Excellent communication (e.g., oral, written, presentation) and interpersonal relationship skills.
  • Proficiency in general computer software such as word processing, spreadsheets, presentations.
  • Understanding of Good Manufacturing Practices (GMP).