We are currently seeking a Senior Product Development Engineer for one of our clients in Canton of Neuchatel.
If you are looking to work in a dynamic and very friendly working environment and in the medical devices sector then this is for you.
This is an open-ended temporary contract
Please note this vacancy requires fluency in French.
The Senior Product Development Engineer works as a member of sustaining engineering team on
development of products in Integra’s drainage portfolio to the latest compliance standards.
The Senior Product Development Engineer will be responsible for design modifications of existing
products including full product development cycle required by the latest quality system.
Your responsibilities:
Understanding of Medical Device-New product development and Sustaining Engineering Process,
Working knowledge of Technical files and Medical Device product development process,
Knowledge of current European Medical Device directives (MDD/MDR) and CE Mark process,
Experience in performing/coordinating projects involving design process,
Experience in QMS, Tech File, DHF and Risk Management File,
Understanding of Medical regulatory standards is preferred (EU Regulations – MDD & MDR)
Knowledge on Part 820, Part 11, ISO 13485, MDD/IVDD, IEC 60601x, IEC 62304, ISO 14971,
Knowledge in DFMEA, PFMEA, GD&T and Design documentation processes,
Experience in creation of Protocols, Testing and Verification including product usability is required,
Should be capable of owning the project ownership from beginning to project completion,
Hardworking and should be individual working for design and good Problem-solving skills,
Should have good communication skills to be able to communicate with steak holders, project managers, outside vendors,
Experience with MS Project, MS Office
Your profile:
Experience: minimum 5 years’ experience in mechanical design and new product development of medical devices
Education: Bachelor’s degree in Mechanical Engineering or similar engineering discipline (Master’s degree in mechanical or biomedical engineering preferred)
Strong time/project management skills (preferably experience using Microsoft Project or another project management software)
English and French fluent
We are currently seeking a Senior Product Development Engineer for one of our clients in Canton of Neuchatel.
If you are looking to work in a dynamic and very friendly working environment and in the medical devices sector then this is for you.
This is an open-ended temporary contract
Please note this vacancy requires fluency in French.
The Senior Product Development Engineer works as a member of sustaining engineering team on
development of products in Integra’s drainage portfolio to the latest compliance standards.
The Senior Product Development Engineer will be responsible for design modifications of existing
products including full product development cycle required by the latest quality system.
Your responsibilities:
Understanding of Medical Device-New product development and Sustaining Engineering Process,
Working knowledge of Technical files and Medical Device product development process,
Knowledge of current European Medical Device directives (MDD/MDR) and CE Mark process,
Experience in performing/coordinating projects involving design process,
Experience in QMS, Tech File, DHF and Risk Management File,
Understanding of Medical regulatory standards is preferred (EU Regulations – MDD & MDR)
Knowledge on Part 820, Part 11, ISO 13485, MDD/IVDD, IEC 60601x, IEC 62304, ISO 14971,
Knowledge in DFMEA, PFMEA, GD&T and Design documentation processes,
Experience in creation of Protocols, Testing and Verification including product usability is required,
Should be capable of owning the project ownership from beginning to project completion,
Hardworking and should be individual working for design and good Problem-solving skills,
Should have good communication skills to be able to communicate with steak holders, project managers, outside vendors,
Experience with MS Project, MS Office
Your profile:
Experience: minimum 5 years’ experience in mechanical design and new product development of medical devices
Education: Bachelor’s degree in Mechanical Engineering or similar engineering discipline (Master’s degree in mechanical or biomedical engineering preferred)
Strong time/project management skills (preferably experience using Microsoft Project or another project management software)
English and French fluent