Validation Engineer - US, New Jersey - 6 Month ContractReady to take your career to the next level with a global life sciences organisation that’s shaping the future of drug development? We’re partnering with a pioneering pharmaceutical manufacturing company based in New Jersey to find driven, talented professionals who thrive in fast-paced, high-impact environments.
This is your opportunity to work at the cutting edge of science and manufacturing - collaborating with industry experts, contributing to breakthrough therapies, and playing a key role in delivering life-changing solutions to patients worldwide.
If you’re ambitious, detail-oriented, and passionate about making a difference, this could be the role that defines your next chapter.
What you'll do:
- Generating and executing qualification documents: (IQ/OQ/PQ Protocols
- This can include, but is not limited to, the following qualification types: Equipment, Facilities/HVAC (temperature mapping, HVAC modification validations, etc.), Critical Utilities (Purified Water Systems, Utility Tie-Ins, etc.), Contained Charging Processes for API manufacturing
- Closeout of aforementioned qualifications, including generation of Summary Reports and closure of Veeva (Change Management System) action items.
- This role will primarily serve to support scheduled Capital Projects, as well as any plant/production support projects that arise during the term of this contract (corrective measure qualifications, process improvements, etc.)
What you'll need:
- Extensive experience as a Validation Engineer/Scientist with a background in the project types mentioned above
- Ability to multitask and work independently with minimal assistance or guidance
- Detail oriented with good organization and communication skills
If this role is of interest, apply now!
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