Supervisor - Parenteral Manufacturing Operations 1st Shift

Eli Lilly Eli Lilly · Pharma · Pleasant Prairie, WI

Supervises parenteral manufacturing operations on the 1st shift, focusing on safety, quality, and operational improvements in a state-of-the-art facility. Responsibilities include direct line supervision, employee development, ensuring compliance with policies and procedures, participating in commissioning and qualification, and collaborating with cross-functional teams. The role requires a strong understanding of FDA guidelines and cGMP requirements, with experience in aseptic or sterile manufacturing environments preferred.

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. Actively participate in commissioning and qualification activities as the site prepares for initial manufacturing operations, including equipment walkthroughs, procedure reviews, and operator readiness assessments.
  4. Partner with cross-functional teams (Engineering, TSMS, Quality, etc.) to support the transition from line ramp-up to routine production.
  5. Leads and participates in structured problem-solving (root cause analysis, countermeasure development, etc.) to improve safety, quality, and operational performance.

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
  • Authorized 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

  • 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