Develop manufacturing tools, fixtures, jigs and product parts and assemblies including design, documentation (including SOPs) to drive process improvements.
Support to process validation (and IQ/OQ/PQ) including writing, executing, results analysis and reporting of TEST protocols and reports.
Work with Production Quality to resolve manufacturing and quality problems related to methods, processes, tooling, equipment and product design.
Create engineering drawings and specifications.
Create protocols, reports, SOPs and associated documentation.
Support maintenance activities
Requirements: Hands-on - technical with experience in manufacturing/engineering environment 5-10 years, Independent in leading Projects and tasks.
Aware of and comply with medical device Quality Management system
Knowledge and understanding of document control, design transfer, verification, validation, acceptance activity, DMR, DHR.
Mechanical design in CAD software - SolidWorks (an advantage)
Proficient in English and Hebrew
אם תבחר/י להציג את מועמדותך ולשלוח קורות חיים, פרטיך ישמרו במאגרי המידע של קבוצת חבר.
This position is open to all candidates.