Team Lead Validation

11 hours ago

Beit HaEmek, Israel Sartorius Stedim Full time ₪120,000 - ₪180,000 per year
Leading a team of validation engineers.

• Responsible for validation of process equipment and supporting systems for the production of sterile media.

• ​​Writing and executing protocols and reports - IQ, OQ, PQ for equipment.

• Full responsibility for Cleaning Validation - planning, execution and coordination with analytical laboratories.

• Planning and managing engineering projects while complying with GMP and FDA, EMA (Ministry of Health) regulations.

• Managing tasks, prioritizing and monitoring team schedules.

• Ongoing interface with QA, operations, maintenance, production, laboratories and R&D departments.

• Supporting the handling of exceptions, risk analysis and failure investigation.

• Promoting continuous improvement and implementing new procedures and standards.

Job Description:

• Leading a team of validation engineers.

• Responsible for validation of process equipment and supporting systems for the production of sterile media.

• ​​Writing and executing protocols and reports - IQ, OQ, PQ for equipment.

• Full responsibility for Cleaning Validation - planning, execution and coordination with analytical laboratories.

• Planning and managing engineering projects while complying with GMP and FDA, EMA (Ministry of Health) regulations.

• Managing tasks, prioritizing and monitoring team schedules.

• Ongoing interface with QA, operations, maintenance, production, laboratories and R&D departments.

• Supporting the handling of exceptions, risk analysis and failure investigation.

• Promoting continuous improvement and implementing new procedures and standards.

Job requirements:

• Bachelor's degree in engineering (chemical, biomedical, biotechnology, pharmaceuticals).

• At least 3 years of experience in validating process equipment - especially in a sterile environment.

• Deep familiarity with CIP/SIP cleaning processes including cleaning validation.

• Experience in writing protocols and IQ/OQ/PQ reports.

• Understanding of GMP regulations and regulatory requirements for sterile manufacturing systems.

• Management experience or leading teams/projects.

• Ability Working in a dynamic environment.


• Living in the northern region (Nahariya, Acre, Karmiel and the surrounding area).

About Sartorius 

Sartorius is part of the solution in the fight against cancer, dementia, and many other diseases. Our technologies help translate scientific discoveries into real-world medicine faster, so that new therapeutics can reach patients worldwide. 

We look for ambitious team players and creative minds, who want to contribute to this goal and advance their careers in a dynamic global environment.

Join our global team and become part of the solution. We are looking forward to receiving your application. 

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