We're Hiring: Process Validation Engineer – Princeton, NJ

Location : Princeton, NJ (Onsite)

We are seeking an experienced Process Validation Engineer with 5+ years in pharmaceutical manufacturing . The ideal candidate will be responsible for executing and managing IQ, OQ, PQ validation activities and ensuring compliance with FDA and cGMP standards.

Key Responsibilities :

• Lead and execute process validation for pharmaceutical manufacturing systems.
• Ensure compliance with FDA 21 CFR Part 211 , cGMP , and regulatory standards.
• Develop and review validation protocols and documentation (reports, SOPs).
• Collaborate with engineering , QA , and operations teams for process optimization.

Requirements :

• 5+ years of experience in process validation in the pharmaceutical industry .
• Strong understanding of FDA regulations , cGMP , and validation processes .
• Excellent communication and cross-functional collaboration skills.