Quality Control Laboratory Analyst (Raw Materials)

Role: Quality Control Analyst responsible for raw materials and product testing in the manufacture of clinical and commercial gene therapies. Responsibilities: perform cGMP material inspections and testing, review analytical data for compliance, participate in investigations and protocol/report development, update QC documentation, support document control and USP standards, and maintain laboratory equipment. Requirements: Bachelor's in life sciences or related field; experience with pH, Osmo, Endotoxin, cell culture, FBS testing preferred; proficiency in SOP adherence, scientific writing, and MS Office. HighValue: focus on gene therapy manufacturing, cGMP compliance, in-house raw material and finished product testing, laboratory investigations, and quality documentation. WorkSetup: not specified; likely on-site at Pittsburgh facilities.