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Lead Operator - Formulation​/Preparation; Night Shift

Job in Pleasant Prairie, Kenosha County, Wisconsin, 53158, USA
Listing for: BioSpace
Full Time position
Listed on 2026-07-08
Job specializations:
  • Pharmaceutical
    Pharmaceutical Manufacturing
Salary/Wage Range or Industry Benchmark: 35762 - 52459 USD Yearly USD 35762.00 52459.00 YEAR
Job Description & How to Apply Below
Position: Lead Operator - Formulation/Preparation (Night Shift)

At Lilly, the work is demanding because patients are waiting. We unite caring with discovery to help make life better for people around the world, knowing that every decision, every detail, and every day matters. Headquartered in Indianapolis, Indiana, our over 50,000 employees worldwide take on complex challenges to discover and deliver life‑changing medicines, strengthen how health is understood and managed, and support the communities we serve.

This is hard, urgent, selfless work—but it’s work worth doing. If you’re driven by purpose and ready to bring your best to work that truly matters for patients, we invite you to join us.

Organization Overview

We serve an extraordinary purpose. For more than 140 years, we have worked to discover medicines that make life better. These discoveries start in Lilly Research Laboratories, where our scientists work to create new medicines that will help solve our world’s greatest health challenges. We explore how next generation therapeutics, new technologies, and data analytics can improve patient health and the healthcare system.

Our team shares a real passion for challenging conventional wisdom and creating an environment that embraces creative, breakthrough concepts.

Responsibilities
  • During the project phase, the Operations Line Lead – Formulation/Preparation will support commissioning/qualification activities required to bring the formulation suite into service as well as support site operational readiness activities. This role will become a subject‑matter expert for the formulation and preparation equipment process and will be directly involved with training future new hires.
  • After project phase completion, the role will be responsible for line (suite) leadership, daily operations, development of operators, requalification tasks, ensuring compliance with all policies and procedures, and ensuring resources are scheduled accordingly per the daily production plan.
Key Objectives
  • Provide commissioning, qualification, and operational readiness support during the project phase.
  • Support Site Leadership to build a diverse and capable site organization by delivering area operational procedures, quality processes and controls for the Formulation area.
  • Provide frontline leadership on the manufacturing floor ensuring a high level of safety, quality and productivity to maintain reliable supply of products to patients.
  • Act as a key resource for troubleshooting and function as the primary point of contact for unexpected floor events.
  • Coordinate and deploy technical training and ensure all operators are qualified to perform tasks.
  • Assist the Supervisor in the development and performance evaluations of shift operators.
  • Act as a liaison between operations and support functions.
  • Operate the equipment and lead shift operations to meet production demands.
  • Assist in checking execution documentation (Mastercontrol, SAP, Cleaning Logs, etc.).
  • Drive key departmental objectives including improving safety performance, reducing deviations, improving productivity, and ensuring training compliance.
  • Serve as the backup for the Supervisor.
Basic Requirements
  • High School Diploma or equivalent.
  • Minimum 2–5 years relevant experience in pharmaceutical or medical device manufacturing (education may be substituted for experience with manager discretion). Demonstrated leadership skills with the ability to train and mentor peers.
  • Ability to communicate effectively (written and verbal).
  • Flexibility and problem‑solving skills.
  • Basic digital literacy (desktop software) is required.
  • Must be able to lift 45 lbs.
  • Ability to work 12‑hour shifts (2‑2‑3 schedule) with additional overtime as needed.
  • Knowledge of current Good Manufacturing Practices (cGMPs).
  • Previous experience with compounding/formulation in a Grade C environment.
  • 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 position.
Additional Skills/Preferences
  • Experience with pH meters, water baths, API dispensing, autoclave, and filter integrity testing.
  • Scientific/technical degrees or certifications.
  • Previous experience…
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