Lead engineering activities, report to Engineering Project Manager
Lead & Perform verification and validation activities, 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, 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
2+ years experience in medical device development companies
Problem solving ability, analytical ability, good communication skills
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
2+ years experience in medical device development companies
Problem solving ability, analytical ability, good communication skills
Proficiency with Solidworks or equivalent software
High level written and verbal English
This position is open to all candidates.
