Job-ID Reference Job summary:
We are seeking an experienced Validation Specialist to support validation activities in a GMP-regulated environment.
Roles and Responsibilities: 10 years of experience in Validation within Pharma, Biotech, or Life Sciences. Hands-on experience with IQ, OQ, and PQ. Experience with equipment, facility, utility, or process validation. Strong knowledge of GMP, GxP, and FDA regulations. Experience developing and executing validation protocols and reports. Experience with deviations, CAPA, change controls, and risk assessments. Experience supporting FAT/SAT, commissioning, and qualification activities. Strong technical writing and documentation skills. Ability to work with Engineering, Quality, Manufacturing, and Validation teams.
We are seeking an experienced Validation Specialist to support validation activities in a GMP-regulated environment.
Roles and Responsibilities: 10 years of experience in Validation within Pharma, Biotech, or Life Sciences. Hands-on experience with IQ, OQ, and PQ. Experience with equipment, facility, utility, or process validation. Strong knowledge of GMP, GxP, and FDA regulations. Experience developing and executing validation protocols and reports. Experience with deviations, CAPA, change controls, and risk assessments. Experience supporting FAT/SAT, commissioning, and qualification activities. Strong technical writing and documentation skills. Ability to work with Engineering, Quality, Manufacturing, and Validation teams.
Validation Specialist in newark at Unknown Company
This position is listed as full time and onsite.