Senior CQV Validation Engineer – GMP Biotech CDMO
Job in
Pennington, Mercer County, New Jersey, 08534, USA
Listed on 2026-07-07
Listing for:
Initial Therapeutics, Inc.
Full Time
position Listed on 2026-07-07
Job specializations:
-
Pharmaceutical
Validation Engineer, Pharmaceutical Manufacturing, Pharma Engineer
Job Description & How to Apply Below
Initial Therapeutics, Inc. is looking for a Validation Specialist in Pennington, New Jersey to support commissioning, qualification, and validation (CQV) activities in a GMP manufacturing setting. The ideal candidate will have 9 years of experience in the drug/biologics industry, particularly within biotechnology and pharmaceutical facilities.
The role involves documenting validation protocols, facilitating technology transfers, and ensuring compliance with regulatory requirements. Benefits include comprehensive health insurance and a supportive work culture.
#J-18808-LjbffrPosition Requirements
10+ Years
work experience
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