Supervisor - Parenteral Manufacturing Operations 2nd Shift

Eli Lilly Eli Lilly · Pharma · Pleasant Prairie, WI

Supervisor for Parenteral Manufacturing Operations at Eli Lilly, focusing on direct line supervision of operators, ensuring safety and quality, and driving operational improvements in a pharmaceutical manufacturing setting. Requires experience in regulated environments and cGMP compliance.

What you'd actually do

  1. Responsible for maintaining a safe work environment, working safely and accountable for supporting all HSE Corporate and Site Goals.
  2. Ensure strict compliance with established policies/procedures (Safety, Production Procedures, Sanitization, Gowning, Etc.), ensure operators are trained appropriately.
  3. Take ownership for implementation of countermeasures associated with audits, observations, inspection findings, and deviations.
  4. Participate in planning of equipment prep, formulation, and filling operations. Network with various areas to verify components and equipment are available for orders.
  5. Actively participate in commissioning and qualification activities as the site prepares for initial manufacturing operations, including equipment walkthroughs, procedure reviews, and operator readiness assessments.

Skills

Required

  • 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
  • Ability to work in the United States on a full-time basis

Nice to have

  • 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 actions.
  • Familiarity with root cause analysis and structured problem-solving methods.
  • Comfort working in classified areas (e.g., isolators, Grade C environments) and reinforcing proper technique and compliance.
  • Demonstrated ability to coach, develop, and provide performance feedback to hourly operations personnel.
  • Experience leading teams in a multi-shift manufacturing environment.
  • Ability to set expectations, maintain operational discipline, and drive accountability on the shop floor.
  • Strong judgment and escalation skills in safety, quality, and operational decision-making.
  • Proven ability to work cross-functionally with Quality, TSMS, Engineering, Maintenance, Supply Chain, etc.
  • Effective communicator with the ability to translate procedures and expectations into clear direction for operators.
  • Adaptability to support new equipment, process changes, and capital project activities.
  • Computer proficiency and comfort using enterprise systems and quality management systems (such as SuccessFactors, Veeva Vault, MasterControl, TrackWise, SAP).

What the JD emphasized

  • 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 and 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
  • Strong working knowledge of GMPs, quality systems, and documentation practices in a regulated manufacturing setting.