Systems & Equipment Validation Engineer

Systems & Equipment Validation Engineer at Taro Pharmaceutical Industry (Position 723)

How will your day look like?

• You will be responsible for implementing validation processes for equipment and systems, in compliance with FDA, GMP, and ISO standards.

• Participate in the characterization process for new systems or modifications to existing systems.

• Conduct risk assessments.

• Write validation protocols and perform tests, including periodic reviews.

• Participate in the analysis of equipment and system failures and events.

• Support during audits, initiate necessary adjustments and improvements in existing validation processes.

Required Skills for the Role:

• Bachelor’s degree in Mechanical Engineering, Chemistry, Biotechnology.

• Minimum of 2 years of experience in validation/ quality Assurance.

• Familiarity with working in a GMP environment.

• Organizational skills, system-oriented perspective, ability to handle multiple tasks.

• Ability to work independently and as part of a team, excellent interpersonal skills, and the ability to motivate interfaces.

 • High-level English – speaking, reading, and writing.

 • Familiarity with AutoCAD – an advantage.