עדיין מחפשים עבודה במנועי חיפוש? הגיע הזמן להשתדרג!
במקום לעבור לבד על אלפי מודעות, Jobify מנתחת את קורות החיים שלך ומציגה לך רק משרות שבאמת מתאימות לך.
מעל 80,000 משרות • 4,000 חדשות ביום
חינם. בלי פרסומות. בלי אותיות קטנות.
Are you a Chemical Engineering or Biotechnology Engineering graduate looking to launch your career in the biopharmaceutical industry?
A leading biopharmaceutical company is looking for a QA Computer Systems Validation (CSV) Coordinator to join its Quality Assurance team. This is an excellent opportunity to build expertise in one of the industry's most in-demand fields, combining Quality Assurance, Engineering, Computerized Systems, and GMP regulations.
You'll receive hands-on training and work alongside experienced professionals in a highly regulated manufacturing environment.
What you'll do:
• Support validation activities for computerized systems, equipment, and engineering infrastructure
• Review validation documentation and controlled GMP documents
• Participate in change controls, risk assessments, and validation investigations
• Work closely with QA, Engineering, Manufacturing, and IT teams
• Take part in engineering projects as the QA representative
• Gain practical experience with Computer Systems Validation (CSV) in a GMP-regulated environment
Requirements:
✔ B.Sc. in Chemical Engineering or Biotechnology Engineering (required)
✔ Strong technical aptitude and interest in computerized systems
✔ Excellent analytical skills and attention to detail
✔ Fluent Hebrew and English
✔ Experience in QA, validation, pharmaceuticals, or medical devices is an advantage—but not required
If you're looking for a career path that combines engineering, technology, and quality in a cutting-edge biopharmaceutical environment, we'd love to hear from you!
במקום לעבור לבד על אלפי מודעות, Jobify מנתחת את קורות החיים שלך ומציגה לך רק משרות שבאמת מתאימות לך.
מעל 80,000 משרות • 4,000 חדשות ביום
חינם. בלי פרסומות. בלי אותיות קטנות.