GLP QA Specialist II

Role: QA specialist focused on GLP quality systems within a biotech/pharma setting. Objectives: maintain and improve GLP compliance, document control, and laboratory documentation processes. Responsibilities: manage GLP document systems, laboratory notebooks, and QA reports; support GLP testing and audits; create trend reports on QA metrics; partner with cross-functional teams to ensure quality standards. Qualifications: BS/BA in Life Sciences; 1-3 years QA experience in biotech/pharma; strong knowledge of EDMS, cGMP/GLP, MS Office; excellent communication skills; ability to work independently and collaboratively. HighValue: GLP compliance, document control, QA metrics, laboratory documentation, biotech/pharma industry, cGMP/GLP regulations. WorkSetup: not specified in description.