Find & Apply For Validation Engineer Jobs in Jersey City, New Jersey

Summary:

The Validation Engineer will support GMP validation activities and equipment qualification in a pharmaceutical or life sciences environment. The role involves developing and executing Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) protocols, reviewing validation documentation, preparing reports, and supporting deviation investigations. The engineer will ensure compliance with c

GMP, GAMP, 21 CFR

Part 11, Good Documentation Practices (GDP), and data integrity requirements.

Roles and Responsibilities:

Support equipment qualification and GMP validation activities, including IQ, OQ, and PQ. Develop, execute, and review validation protocols, test scripts, and qualification documents. Prepare validation summary reports and maintain accurate documentation in accordance with cGMP requirements. Support validation deviation investigations, root cause analysis, and corrective and preventive actions (CAPA). Ensure compliance with GAMP guidelines, 21 CFR Part 11, GDP, and data integrity standards. Review validation records for completeness, accuracy, traceability, and regulatory compliance. Collaborate with Quality Assurance, Engineering, Manufacturing, and other cross-functional teams. Support qualification of cell therapy manufacturing equipment, where applicable. Maintain validation documentation and ensure readiness for internal and external audits.

Education & Experience:

Required:

Bachelor's degree in engineering, Life Sciences, Biotechnology, Chemistry, or a related scientific discipline.

Preferred:

Relevant coursework or training in pharmaceutical validation, equipment qualification, GMP, or quality systems. Minimum of 5+ year of cGMP experience in the pharmaceutical, biotechnology, or life sciences industry. Hands-on experience supporting equipment qualification and validation activities, including

IQ/OQ/PQ.

Experience preparing, executing, and reviewing validation protocols and reports. Knowledge of c

GMP, GAMP, 21 CFR

Part 11, GDP, and data integrity principles. Experience supporting validation deviations and investigation documentation.

Preferred:

Cell therapy manufacturing equipment qualification experience.