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.