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Operator-Filling/Manufacturing

Eli Lilly and Company

Pleasant Prairie (WI)

On-site

USD 40,000 - 70,000

Full time

30+ days ago

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Qualifications

  • High School Diploma or GED required; STEM degree preferred.
  • Strong communication and flexibility in troubleshooting challenges.

Responsibilities

  • Support start-up activities and ensure continuous supply of medicines.
  • Provide leadership on the manufacturing floor for safety and quality.

Skills

Effective Communication
Flexibility in Troubleshooting
Computer Proficiency (MS Office)
Leadership and Training
Knowledge of CGMPs
Experience in Manufacturing
Continuous Improvement (Lean, Six Sigma)

Education

High School Diploma or GED
STEM Degree or Certifications

Tools

Manufacturing Execution Systems
Electronic Batch Record

Job description

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 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.

Responsibilities

The Parenteral (PAR) Operators (Entry to Expert roles) will support start-up activities at Eli Lilly’s newly acquired Kenosha County site. This role is required to bring the area into service which may include formulation, aseptic isolator barrier filling, and equipment preparation. They will become the experts within their assigned area and educate their team in the proper operation of the facility. This position may require travel (2-4 week trips and/or 3-12 month short-term assignments) domestically with the opportunity for travel internationally to collaborate, train with, and learn from sites that currently produce our medicines.

After the project phase is complete, this role will be responsible for ensuring continuous supply of our medicines by expertly running the process, troubleshooting, collaborating cross-functionally, and holding all to our safety first/quality always mindset. Operators will support daily activities to meet capacity plans while developing their own and our team’s capabilities.

Key Objectives/Deliverables:

Integrity

  • Provide leadership on the manufacturing floor ensuring high levels of safety, quality, and productivity to maintain a reliable supply of products to patients.
  • Responsible for maintaining a safe work environment, exemplifying safe working practices, and being accountable for supporting HSE goals.
  • Act as both administrator and technical leaders for operations. Set a good example through demonstrated knowledge of procedures, compliance with quality systems, and teaching of proper techniques.

Excellence

  • Technical leader: Key resource for troubleshooting and functions as the primary point of contact for issue escalation on the production floor.
  • Responsible for administering technical training and ensuring all operators are trained to perform tasks.
  • Operate the equipment and perform activities as required to meet the production schedule.
  • Assist in checking execution documentation (Electronic Batch Record, SAP, Cleaning Logs).
  • Drive key departmental objectives including improving safety performance, reducing deviations, improving productivity, and training compliance.

Respect for People

  • Support Site Leadership to build a diverse and capable site organization by delivering area operational procedures, quality processes, and controls for the PAR areas.
  • Key liaison between operations and support functions.

Basic Qualifications

  • Minimum education: High School Diploma or GED.
  • Ability to effectively communicate (electronically, written, and verbal).
  • Flexibility - the ability to troubleshoot and triage challenges.
  • Computer proficiency (desktop software, MS Office).

Time Commitments and Work Authorization

  • Must pass a “fitness for duty” physical exam.
  • Shift flexibility.
  • Ability to work overtime as required.
  • Ability to wear safety equipment (glasses, shoes, gloves, etc.).
  • Ability to work and gown in a cleanroom (Grade C, ISO 8) environment.
  • Ability to participate in professional development opportunities.
  • Qualified candidates must be legally authorized to be employed in the United States. Lilly does not anticipate providing sponsorship for employment visa status (e.g., H-1B or TN status) for this employment position.

Additional Skills/Preferences

  • Experience with, completion of, or understanding of leadership and the ability to train/educate team members.
  • STEM degree or certifications.
  • Aseptic filling, single-use assemblies, isolator technology.
  • Knowledge of current Good Manufacturing Practices (CGMPs).
  • Experience in operations or manufacturing environments.
  • Manufacturing Execution Systems and electronic batch release.
  • Continuous improvement (Lean, Six Sigma methodologies).

This job description is intended to provide a general overview of the job requirements at the time it was prepared. The job requirements of any position may change over time and may include additional responsibilities not specifically described in the job description. This position requires flexibility and a commitment to meeting operational needs, which may involve working irregular hours or shifts, including swing shifts. Your dedication to meeting these scheduling requirements will contribute significantly to the success of our operations and the quality of our products.

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