Pharmaceutical Manufacturing Operator

Role: Manufacturing Operator supporting GMP manufacturing of advanced therapies, including gene therapy, at Lilly’s new Lebanon facility. Responsibilities: conduct routine production activities in cleanroom environments, support equipment qualification and validation, ensure compliance with cGMP and safety standards, coordinate with quality and maintenance teams, and document processes accurately. Qualifications: high school diploma or equivalent, 3+ years pharma manufacturing or equivalent experience, hands-on expertise with bioreactors, purification, and cell culture, and familiarity with GMP regulations. Preferred skills include problem-solving, good communication, attention to detail, and ability to learn digital systems. Experience in drug substance manufacturing, particularly with biologics or gene therapy modalities, and working in fast-paced, evolving environments are advantageous. The role initially involves day shifts during startup, transitioning to rotating 4x10-hour shifts once operational. High-value specifics include manufacturing biologics/gene therapies, involvement in equipment validation, and startup of a state-of-the-art facility for clinical and commercial supply. The position reports to shift supervisors and requires adherence to safety protocols, with some overtime expected.