Lead D D activities, report to R D Director
Lead Perform verification and validation activities including planning, protocols and reports
Lead Perform bench testing and reports
Design of Experiments, device improvements, risk analysis etc.
Manufacturing process development
Manufacturing process control
Transfer to production activities, NPI and process validation activities
Lead Perform verification and validation activities including planning, protocols and reports
Lead Perform bench testing and reports
Design of Experiments, device improvements, risk analysis etc.
Manufacturing process development
Manufacturing process control
Transfer to production activities, NPI and process validation activities
Requirements:
B.Sc. in Biomedical/Mechanical Engineering
Familiar with medical device regulatory environments ISO13485, FDA and ISO14971
5+ years experience in medical device development companies
Experience in project leading
Problem solving ability, Analytical ability
Good communication skills, Independence and high sense of responsibility
Proficiency with Solidworks or equivalent software
High level written and verbal English
B.Sc. in Biomedical/Mechanical Engineering
Familiar with medical device regulatory environments ISO13485, FDA and ISO14971
5+ years experience in medical device development companies
Experience in project leading
Problem solving ability, Analytical ability
Good communication skills, Independence and high sense of responsibility
Proficiency with Solidworks or equivalent software
High level written and verbal English
This position is open to all candidates.
