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Job type: Contract

Discipline: Manufacturing

Location: United Kingdom

Are you passionate about quality and precision? Join our client with this engineering role and help ensure top-tier standards every day.

Proclinical is seeking a skilled engineer to join a dynamic team in Cambridge, UK. In this role, you will provide expertise in design control and risk management for medical devices and combination products throughout their lifecycle. You will collaborate with cross-functional teams to ensure compliance with quality and regulatory standards while supporting clinical trials and commercial licensures. This is an exciting opportunity to contribute to innovative biotherapeutic solutions.

Responsibilities:

Lead design control and risk management activities for combination product development programs.
Author, review, and maintain design history files and risk management documentation.
Facilitate risk management activities with external design companies and manufacturing facilities.
Ensure compliance with internal and external quality and regulatory standards.
Support design validation processes, including human factors engineering assessments.
Assess external design companies and suppliers for quality systems and capabilities.
Investigate device design and manufacturing issues from clinical trials and commercial use.
Contribute to regulatory submission data and content for assigned projects.
Support internal and external audits of the Quality Management System.
Identify and implement strategies to improve combination product systems.

Key Skills and Requirements:

Background in science or engineering (e.g., chemistry, biology, biomedical sciences, mechanical engineering, materials sciences, or related disciplines).
Expertise in ISO 13485, ISO 14971, 21 CFR 820, 21 CFR 4, and EU Medical Devices Regulation.
Experience in design controls and risk management for combination products.
Familiarity with Human Factors Engineering and usability engineering principles.
Knowledge of device assembly and manufacturing processes.
Strong analytical skills for complex data analysis.
Proficiency in project management methodologies and technical leadership.
Excellent communication and collaboration skills.
Proficiency in general computer software (e.g., word processing, spreadsheets, presentations).
Understanding of Good Manufacturing Practices (GMP).

If you are having difficulty in applying or if you have any questions, please contact Dean Fisher at d.fisher@proclinical.com.

If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page.

Proclinical is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Proclinical is acting as an Employment Agency in relation to this vacancy.

By submitting this application, you confirm that you've read and understood our privacy policy, which informs you how we process and safeguard your data - https://www.proclinical.com/privacy-policy.