Responsibilities

• Conduct equipment, process, cleaning, and computerized system validation.

• Prepare and update validation protocols and reports.

• Perform routine validation tests to ensure compliance with GMP and company standards.

• Coordinate with production, QA, and QC during validation activities.

• Monitor and document validation results accurately.

• Ensure all validated systems remain within approved specifications.

Qualifications

• Bachelor’s degree in Pharmacy, Chemistry, Engineering, or related field.
• Experience in validation or GMP-regulated manufacturing is an advantage.
• Basic knowledge of GMP, IQ/OQ/PQ, and validation procedures.
• Detail-oriented, organized, and able to follow technical instructions.
• Good communication and documentation skills.