Operator I - 1st (M-F 6am-2:30pm)

Role: Entry-level manufacturing associate responsible for operating equipment, maintaining documentation, and supporting pharmaceutical production in a cGMP environment. Objectives include ensuring safe, efficient operations and compliance with regulatory standards. Responsibilities encompass dispensing raw materials, verifying labels and lot numbers, operating dispensing and processing equipment, maintaining accurate batch records, and supporting quality control through in-process testing and troubleshooting. Qualifications include a High School Diploma or equivalent, with relevant manufacturing experience preferred; knowledge of cGMP, SOPs, safety practices, and basic math required. Skills in documentation, equipment operation, and effective communication are essential. High-value biopharma specifics: familiarity with pharmaceutical manufacturing standards, working in a regulated environment, and understanding of process and equipment troubleshooting. Role involves routine to semi-routine tasks with some problem-solving and judgment within defined practices. Work setup is on-site with exposure to moving mechanical parts, fumes, odors, and dust; occasional walking and extended periods at workstations. The position supports production schedules and requires maintaining safety, quality, and compliance standards.