Key Responsibilities:
Professional
Being the operation’s interface to R&D team for the introduction of new products or for the improvement of existing ones
Drive improvement activities of the production process. Monitor manufacturing processes to identify ways to reduce losses, decrease time requirements, or improve quality
Apply engineering procedures and methods in manufacturing processes
Providing technical support to the purchasing activity
Writing and updating Work Instructions and Test Instructions
Responsible for ECR/ECO process approval and implementation activity
Deviation Forms release
Responsible for definition of maintenance policy for production tooling/jigs/fixtures/equipment
Identify faults, investigate production problems and failures
Definition of control tools for production efficiency measurement
Technical support in substitute components approval
Cost reduction initiatives
Involvement in production planning
Qualifications (Education, Skills, and Experience; Required):
Required:
B.Sc. Electronic engineer, 5 years of experience in overseeing engineering activities in the electronic/medical/mechanical medical device company (Must)
Familiarity with PLM platforms, methodologies, processes and best practices (Must)
Experience with SolidWorks /OrCad
Experience with product files writing, including manufacturing specifications & processes, proof of concept processing (Must)
Experience with subcontractors management
Strong capabilities in leading Multi-Disciplinary projects
Project management skills and ability to work to tight deadlines
Ability to work well under pressure
Must have hands on experience in taking up improvement projects
Good Hebrew & English oral and written skills
Team working, ability to work with others collaboratively
Familiar with ERP system (Priority advantage)
