Validation Engineer - Cleaning and Validation -SGGK3

About the Role

We are seeking Validation Engineers to support equipment, facility, and utility qualification activities in a regulated life sciences manufacturing environment. This contract role is critical to ensuring compliance with GMP/GxP standards and maintaining validated state for critical systems.

Key Responsibilities

• Execute validation protocols for equipment, facilities, and utilities (IQ/OQ/PQ).
• Perform temperature mapping and monitoring using tools such as Kaye AVS.
• Support equipment/facility revalidation activities.
• Author, review, and execute validation lifecycle documentation.
• Collaborate with QA, Engineering, and Manufacturing teams to ensure validation readiness.
• Provide technical input on deviations, CAPA, and risk assessments.

Qualifications & Experience

• Bachelor’s degree in Engineering, Life Sciences, or related discipline.
• 4–6 years of validation engineering experience in pharma/biotech or medical devices.
• Hands‑on experience with Kaye AVS usage, temperature mapping, and revalidation.
• Strong knowledge of GMP/GxP compliance and validation lifecycle.
• Excellent documentation and communication skills.

Contract Details

• Duration: 8 months