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Are you ready to use your device engineering expertise to help develop the next generation of drug delivery technologies that could improve patient outcomes worldwide?

Ñî¹óåú´«Ã½Íøygfcmw¡¤(Öйú)Õ¾Èë¿ÚÖ±½Ó½ø is seeking a Senior Associate Device Engineer to join a dynamic team in the UK. This role focuses on supporting the development and testing of innovative drug delivery devices, including components like syringes and cartridges. You will play a key role in risk assessment, experimental analysis, and ensuring compliance with quality standards. This is an excellent opportunity for someone passionate about engineering and science to contribute to cutting-edge pharmaceutical advancements.

Responsibilities:

• Collaborate with multidisciplinary teams to assess and investigate drug delivery device performance factors.
• Author, review, and manage design control documentation.
• Support interactions with external vendors and internal partners for design assessment, verification, and manufacturing process qualification.
• Develop and validate test methods, experimental rigs, and setups.
• Contribute to early-stage usability and market research studies to identify user requirements.
• Design and evaluate test rigs and challenge parts.
• Assess supplier designs, identify critical areas, and mitigate potential failure modes.
• Conduct risk management activities, including input to dFMEA and uFMEA.
• Apply statistical and engineering expertise to solve problems and support decision-making.
• Analyze data using statistical tools to quantify device performance and controlling parameters.
• Operate laboratory equipment and ensure compliance with SOPs and risk assessments.
• Manage ISO 13485-related documentation, including change control and instrument compliance.
• Prepare scientific reports and ensure accurate data transcription and analysis.
• Perform additional duties as required to support business goals.

Key Skills and Requirements:

• Degree or equivalent qualification in a relevant Science or Engineering discipline.
• Strong knowledge of mechanical and/or electronic testing of drug delivery devices.
• Experience in test method development, validation, and device lifecycle management.
• Familiarity with design assessment, specification setting, and analytical method development.
• Proficiency in CAD software (preferably Creo) and engineering calculations.
• Understanding of GLP/GMP, laboratory safety, and ISO 13485 standards.
• Skilled in using scientific measuring and testing equipment.
• Excellent problem-solving, communication, and organizational skills.
• Ability to work independently and collaboratively within multidisciplinary teams.
• Flexible, adaptable, and detail-oriented with a commitment to quality and excellence.
• Willingness to travel or relocate to the Cambridge area if required.

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

Apply Now:

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.

Ñî¹óåú´«Ã½Íøygfcmw¡¤(Öйú)Õ¾Èë¿ÚÖ±½Ó½ø is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Ñî¹óåú´«Ã½Íøygfcmw¡¤(Öйú)Õ¾Èë¿ÚÖ±½Ó½ø is acting as an Employment Agency in relation to this vacancy.

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