Validation & Engineering Group, Inc. seeks a Quality Management System (QMS) SME to lead an end-to-end QMS review across GMP records, data integrity, and batch-release processes for FDA/EU-regulated environments.
The ideal candidate has 6+ years in pharmaceutical, biotechnology, or medical device manufacturing, is fully bilingual in English and Spanish, and is able to work on-site in Manatí, Puerto Rico. You will inventory records and system interfaces (ERP/MES/LIMS/eQMS), assess data integrity
#J-18808-LjbffrQMS SME: GMP Compliance & Batch Release Expert in pr at Unknown Company
This position is listed as full time and onsite.