Operator Parenteral Manufacturing at Eli Lilly

Parenteral Operators

The Parenteral Operators will support operational activities at 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. After project phase is complete, this role will be responsible for ensuring continuous supply of our medicines by; expertly running the process, troubleshooting, and 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.

Responsibilities

Integrity: Provide leadership on manufacturing floor ensuring high level of safety, quality, and productivity to maintain 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 production schedule. Assists in checking execution documentation (Electronic Batch Record, SAP, Cleaning Logs). Drives 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) May be asked to work overtime, weekends, off-shifts by request.

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.

Additional Skills/Preferences

Flexibility - the ability to troubleshoot and triage challenges Computer proficiency (desktop software, MS office) Leadership and the ability to train/educate team members STEM degree or certifications Aseptic filling, single use assemblies, isolator technology Automated, semi-automated, and/or manual inspection Knowledge of current Good Manufacturing Practices (CGMPs) Experience in operations or manufacturing environments Pharmaceutical, medical device or food processing industries Manufacturing Execution Systems and electronic batch release Continuous improvement (Lean, Six Sigma methodologies) Highly automated equipment (inspection, packaging, filling, assembly, etc.) SAP, Electronic Batch Records

Ability to work overtime as required Ability to wear safety equipment (glasses, shoes, gloves, etc) Primary location is Kenosha County, Wisconsin Ability to travel (approximately 10%)

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Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status.

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Actual compensation will depend on a candidate's education, experience, skills, and geographic location. The anticipated wage for this position is $17.30 - $34.38.