Supervisor - Parenteral Manufacturing Operations 2nd Shift

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first.

We’re looking for people who are determined to make life better for people around the world.

The Filling Operations Teams are an essential part of Lilly’s Kenosha County (LKC) Parenteral Manufacturing site. We manufacture and fill injectable parenteral products in state-of-the-art facilities to supply patients around the world. This position will work in a new facility with best in class, globally replicated production equipment. Operations team members will work with the latest industry technologies, while learning from global teams, to manufacture key current parenteral products and preparing for upcoming products.

This role will be responsible for direct line supervision of operators on a given shift, providing leadership to parenteral manufacturing teams, and developing technical expertise of employees. The leader will ensure safety and quality behavior in the area and drive technical and operational improvements. During line ramp‑up activities, the role will also support commissioning and qualification activities required to bring manufacturing areas into service, as well as supporting site operational readiness work.

2nd Shift: 2pm-10:30pm.

• Responsible for maintaining a safe work environment, working safely and accountable for supporting all HSE Corporate and Site Goals.
• Ensure strict compliance with established policies/procedures (Safety, Production Procedures, Sanitization, Gowning, Etc.), ensure operators are trained appropriately.
• Take ownership for implementation of countermeasures associated with audits, observations, inspection findings, and deviations.
• Participate in planning of equipment prep, formulation, and filling operations. Network with various areas to verify components and equipment are available for orders.
• Actively participate in commissioning and qualification activities as the site prepares for initial manufacturing operations, including equipment walkthroughs, procedure reviews, and operator readiness assessments.
• Partner with cross-functional teams (Engineering, TSMS, Quality, etc.) to support the transition from line ramp‑up to routine production.
• Identify and elevate issues to appropriate channels.
• Leads and participates in structured problem-solving (root cause analysis, countermeasure development, etc.) to improve safety, quality, and operational performance.
• Responsible for the coaching, development and performance evaluation of Operations personnel.
• Act as both administrator and technical leader for operations, setting a good example through demonstrated knowledge of procedures, compliance with quality systems and use of proper technique.
• Responsible for shop floor execution as it relates to business plan, GMP conformance, and operational excellence.
• Ensure adherence to use of proper technique in isolator and Grade C operational areas.
• Other duties, as assigned.

• High School Diploma or GED
• 2+ years previous experience in operations or directly supporting a pharmaceutical manufacturing operation
• Strong understanding of FDA guidelines and cGMP requirements
• Qualified applicants must be authorized to work in the United States on a full‑time basis. Lilly will not provide support for or sponsor work authorization or visas for this role, including but not limited to F-1 CPT, F-1 OPT, F-1 STEM OPT, J-1, H-1B, TN, O-1, E-3, H-1B1, or L-1

• Technical & Operational
  • Prior experience in parenteral, aseptic, or sterile manufacturing environments.
  • Strong working knowledge of GMPs, quality systems, and documentation practices in a regulated manufacturing setting.
  • Experience supporting investigations, deviations, and implementation of corrective and preventive…