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, te...