QRC Group in Aibonito, Puerto Rico, seeks a qualified Validation Specialist to support GMP-regulated pharmaceutical processes. The role requires 1–5 years in GMP settings, experience in the pharmaceutical industry, and knowledge of aseptic/regulated processes.
You will develop and execute validation protocols, reports, and SOPs with statistical data analysis. Candidate will work on multidisciplinary projects, ensuring compliance with regulatory requirements and contributing to continuous process
#J-18808-LjbffrGMP Validation Scientist – Pharma Aseptic & Compliance in aibonito at Unknown Company
This position is listed as full time and onsite.