Please note that our offices are now located in the New Industrial Park, Yoqneam. Only CV's written in English will be reviewed. Please click on the "APPLY" button to email your CV.
Quality Reports and follow-ups handling Preparing SOPs, DHRs and other documentation Process validation (IQ/OQ/PQ) Handle changes in Procedure/Place of manufacturing & material in production line Supervising V&V activities Production and R&D support Managing vendor/supplier Quality Managing MRB / CAPA / RMA/ SCAR Performing receiving inspections
- Experience in working with QSR; ISO 13485, 14971; EN 60601; GMP; EN62304; - MDD, FDA compliance – an advantage - 3-5 years of professional experience in QA Engineering, preferably in medical device company - Engineering certification or equivalent experience - Safety ,EMC & RFI challenges in Development & Production stage - an advantage - Fluent English – a must - Experienced Office user – a must - Agile, Priority experience - an advantage
Flexible hours Office Laptop Leased car
© Copyright UltraShape 2009 | Contour I is not yet FDA cleared for sale in the U.S.