Validation Engineer

A pharmaceutical company located in Petah Tikva is seeking a Validation & Projects Engineer for a challenging and dynamic role at a sterile manufacturing facility operating in compliance with GMP requirements.

Job Description:

Responsible for executing validation activities for equipment, systems, manufacturing processes, and computerized systems in accordance with regulatory requirements (GMP, FDA, EMA). Leading engineering projects from planning through implementation. Leading the integration of new equipment and systems into production environments. Collaborating with various departments including production, quality, maintenance, regulatory affairs, and others.

Position Requirements:

- B.Sc. in Engineering – mandatory

- Minimum of 3 years' experience in validation execution and project leadership in the pharmaceutical industry under GMP conditions – mandatory

- Experience in validation of production equipment (e.g., autoclaves, HVAC systems) – mandatory

- Experience in validation of manufacturing processes, scale-up, and cleaning processes – advantage

- Experience in cleanroom construction projects – advantage

- Background in aseptic/sterile manufacturing – advantage

- Excellent English level (written, reading, and spoken) – mandatory

- Strong ability to write and edit technical documents, protocols, and reports

- Excellent interpersonal skills, team player, proactive, independent, with strong technical orientation and analytical abilities