Quality Control Stability Technician

Role: Support daily operations of the QC Stability Department in a biopharma manufacturing setting, ensuring compliance with SOPs and cGMP regulations. Responsibilities: conduct stability sample collection, data entry in LIMS, subaliquoting, receiving and shipping samples, perform preventative maintenance on lab equipment, review stability chamber data, and maintain inventory. Qualifications: high school diploma or GED required; AS/AAS or BA/BS in Life Sciences or related field preferred; relevant experience determined by role level. HighValue: biopharmaceutical stability testing, cGMP compliance, lab maintenance, sample management, within a regulated manufacturing environment. WorkSetup: onsite in Rensselaer, NY, Monday-Friday, 8 am-4:30 pm.