обновлено 14 дней назад
Hardware Mechanical Engineer (Medical Devices)
Вакансия из Hirify Global, списка международных tech-компанийДля мэтча и отклика нужен Plus
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
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TL;DR
Hardware Mechanical Engineer (Medical Devices) (CAD/mechanical design): Developing mechanical components and assemblies across the full product lifecycle, from concept and detailed design through verification and production transfer, with an accent on robust design, engineering drawings, and practical risk reduction. Focus on creating CAD models, prototyping and testing, solving design challenges, and progressing toward subsystem ownership in a multidisciplinary medical technology environment.
Location: On-site in Stevenage, Hertfordshire, United Kingdom; occasional travel to partner sites in Europe and the UK may be required for less than 5% of the time.
Company
operating company Cytiva develops solutions for life sciences, diagnostics, biotechnology, vaccines, medicines, and cell and gene therapies.
What you will do
- Contribute across the full product lifecycle, from early concept and detailed design through verification and transfer into production.
- Own the detailed design and development of mechanical components and assemblies.
- Create and maintain CAD models and engineering drawings.
- Identify design risks early and propose practical, evidence-based solutions.
- Work with senior engineers, technicians, and cross-functional teams to develop robust mechanical solutions.
- Develop technical depth and influence toward future subsystem ownership.
Requirements
- Relevant BA, BSc, MA, or MSc degree in mechanical engineering or a design discipline.
- More than 3 years of experience delivering mechanical solutions.
- Understanding of engineering fundamentals, including materials, tolerancing, and analysis.
- Hands-on experience with prototyping, testing, or product development environments.
- Strong problem-solving skills and the ability to translate requirements into practical designs.
- Ability to travel occasionally to partner sites in Europe and the UK, for less than 5% of the time.
Nice to have
- Experience in medical device design and engineering according to relevant standards such as ISO 13485 and GMP requirements.
- Experience launching devices in the medtech sector.
Culture & Benefits
- Work in a culture focused on belonging, continuous improvement, and tangible impact in life sciences.
- Collaborate with colleagues who care about customers and patients.
- Access healthcare programs and paid time off through 's benefits programs.
- Work on products and challenges connected to biological research, vaccines, medicines, and cell and gene therapies.
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