סקירה כללית
^^משרה זו נלקחה מ Career^^LTS is a leading pharmaceutical technology company that develops and manufactures innovative drug delivery systems for the pharmaceutical industry. LTS´ commercial offering encompasses more than 20 marketed products LTS operates today from 5 sites: Netanya, Israel, Adrenarche, Germany, West Caldwell, NJ, USA, St. Paul, MN, USA, and Shanghai, China. We are looking for an excellent Design QA Engineer to join our team in Israel. The position is hybrid
• 4 days a week from the office, and 1 day from home. Job Description: Be the QA focal point design and development of projects throughout the product design process until transfer to production Provide quick solutions to inquires and problems arising during the process Control all aspects of project documentation Interface with relative personnel to resolve document problems/issues within the design process Be a customer facing team member and represent the organization and QA needs to the customer Assist in cases of non
• conformities (NC) of products, parts and processes Supporting production readiness activities and validations Perform investigations and collect data on deviations of parts, materials or processes throughout the organization, while working with other departments Direct manager: Director of Quality Job Requirements: Education: Practical Engineer/ B.Sc. in Quality/ Biomedical/ Biotechnology or similar
• an advantage CMQ / CQE or similar
• an advantage Job skills: At least 2 year of experience in working according to GMP and regulatory requirements (FDA QSR part 820, ISO 13485)
• mandatory Previous experience in QA design work
• mandatory Experience with QMS and production
• significant advantage Experience in the field of Medical Devices
• an advantage Computer skills: Good knowledge of MS
• Office tools (Excel, Word), Acquaintance with E
• Document management systems Language skills: English
• high level (written and spoken) Personality: Problem solving attitude and mediator Detail
• oriented, dependable and trustworthy Ability to evaluate, prioritize, organize, multitask and problem solving Ability to work in a fast
• paced and deadline
• driven environment Ability to work in a team as well as independently Good analytical skills Self
• starter with drive, focus, and initiative
דרישות המשרה
Education: Practical Engineer/ B.Sc. in Quality/ Biomedical/ Biotechnology or similar
• an advantage CMQ / CQE or similar
• an advantage Job skills: At least 2 year of experience in working according to GMP and regulatory requirements (FDA QSR part 820, ISO 13485)
• mandatory Previous experience in QA design work
• mandatory Experience with QMS and production
• significant advantage Experience in
