Jobs in Edison, NJ

About the role

This is a hands-on commissioning, qualification and validation role with high growth potential. You will work alongside our CQV Lead on facility, utility and equipment qualification programs for pharmaceutical and biotechnology clients — writing and executing protocols, working in the field, and building toward owning systems independently. Clear technical writing. Much of this role is producing documents that a regulator may read.

What you'll bring

• We are looking for someone with real GMP experience who wants to move further into validation than their current role allows.
• Degree in engineering
• Equivalent hands-on experience will be considered in its place.
• microbiology or a life science is preferred.

Benefits