Overview
Mechanical Engineer I role at Cytiva. This position is part of the R&D department located in Grens, Switzerland and will be an on-site role.
What You Will Do
* Contribute to all phases of product development and specifically in the continued maintenance of our Cell Therapy platform through change control, including design, documentation, prototyping, testing, supplier collaboration, industrialization.
* Collaborate with project teams to define and update product specifications and requirements, and translate them into robust mechanical designs through component and assembly geometry, material selection, and performance standards.
* Perform advanced engineering analyses, including complex calculations, dimensioning, tolerancing, and dimensional analysis, to ensure design accuracy and manufacturability.
* Create and maintain detailed 2D and 3D CAD drawings, bills of materials, and engineering specifications, while managing engineering change requests throughout the product lifecycle.
* Lead root cause investigations using structured problem-solving methodologies, and ensure compliance with ISO 13485, ISO 9001, and other applicable quality management system requirements.
Who You Are
* University degree (or equivalent) in mechanical or mechatronic engineering, with 3+ years of successful experience in mechanical design engineering within multidisciplinary environments—ideally in life sciences or medical fields or regulated industries—and a proven track record in developing and sustaining complex, regulated products from concept through detailed design and dimensioning, under a quality management system focused on compliance, quality, and execution rigor.
* Well-founded understanding of mechanical engineering disciplines, including proficiency in using 3D CAD design software and generating 2D drawings optimized for Design For Excellence. Experience with Solidworks is preferred.
* Knowledge and practical experience of relevant regulations (ISO 9001, ISO13485, cGMP), specifically for the US and European market.
* Demonstrated ability to clearly communicate (oral, written) in French and English across global, cross-cultural, cross-functional teams and stakeholders.
* Customer-oriented mindset, autonomous at work, good organizational skills, creative, and comfortable with change.
Nice to have
* Manufacturing processes development associated with a medical device or biological application.
* Demonstrated experience with electrical, electronics and plastic parts design.
* Product Lifecycle Management system.
Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.
#J-18808-Ljbffr