Participate in the design the internal and external mechanical structure of the equipment, develop test plans, perform the verification and validation activities with quality and compliance focus.
Designing mechanical parts, mechanisms and enclosures
Packaging design, manufacture and qualification (Shock, vibration tests, water proofing)
Taking part in product's UL and CE certification
Active interaction with strategic suppliers involved in the development and work occasionally close to the end-users.
Ensure development compliance with GMP requirements
You will be involved in development of high value equipment product You will work for a challenging medical devices company
University degree or equivalent in related scientific or engineering fields (mechanics, micro-mechanics, or similar fields)
Major experience in new product development and manufacturing equipment, ideally for the medical or life science industry involving cross-functional teams.
Demonstrated skills of global, cross-functional project teams and ability to drive project design plans to completion on-time
Demonstrated experience in launching products following formal product development cycle/ methodology and quality management system
Knowledge and practical experience of relevant regulations (ISO 9001, ISO13485, cGMP),
Expertise in CAD design required (ideally Solidworks)
Fluent in English, a second language is a plus
Our client is a leader in its field with an international presence.
