לצערנו המשרה כבר לא בתוקף
Reviewing controlled documents, performing version & lifecycle control.
Reviewing ECOs and CDPs, supervising all approval cycles, checking BOMs, releasing ECOs, checking Objective Evidences of implementation by Contract Manufacturers.
Maintaining and updating list of ECO approvers, determining the relevant approvers depending on change type and project.
Quality assurance professional course is an advantage.
Previous experience in a regulated environment, such as medical devices, is an advantage.
Languages Excellent command of English and Hebrew, both written and oral.
Good computer skills.
Previous experience with document and change management platforms is an advantage.
Thorough and detail oriented approach to work, well-organized, strong attention to details.
Excellent interpersonal skills, both verbal and written. Ability to communicate effectively with other individuals.
Eager to learn, high motivation and dedication.