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Manufacturing Operator

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Lilly

2024-11-13 20:40:51

Job location Burlington, Wisconsin, United States

Job type: fulltime

Job industry: Manufacturing Operations

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 around the world 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.

Position Brand Description:

The Manufacturing Operator will work in the Kenosha County (pleasant Prairie) Parenteral Manufacturing site where Parenteral products for domestic and international markets are manufactured and packaged. The primary purpose of the position is to safely inspect high quality pharmaceutical products utilizing Lilly standards by following good manufacturing practices in controlled facilities. Additionally, the position will require the operation of various automated and semi-automated equipment in manufacturing areas as well as performing manual inspections. The operator will focus on inspecting these high-quality medicines by abiding by the Lilly culture of integrity, excellence, and respect for people.

This position will require travel (2-8-week trips and/or 3-4-month short term assignments) domestically to collaborate, train with, and learn from sites who currently produce our medicines.

Key Objectives / Deliverables:

  • Adhere to Parenteral Plant safety policies and procedures; contribute to a safe work environment.
  • Setup and operations in non-aseptic manufacturing processes, including the set up, use, and/or operation of automated and semi-automated inspection machines in controlled facilities.
  • Adherence to standard operating procedures, current Good Manufacturing Practices, and safety policies / procedures.
  • Document process steps on appropriate batch documentation (paper and electronic).
  • Participate in department meetings, team building, and training activities.
  • Providing input for department SOPs and training.

Minimum Requirements:

  • Experience working in a manufacturing environment.
  • Must pass a post offer physical exam.
  • Must pass eye exam and not be color blind.
  • Authorization to work in the United States without employment visa sponsorship.

Additional Preferences:

  • Experience with GMPs.
  • Ability to work through production issues including basic troubleshooting skills, and use of tools.
  • PMX, Flow-stream or other electronic batch documentation system knowledge.
  • Previous pharmaceutical manufacturing experience.
  • Manual, automated, and semi-automated inspection experience.
  • Strong attention to detail in carrying out of manufacturing conduct and technique, and performing and documenting all production activities on paper and on computer based systems.
  • Basic math skills, including the evaluation of the results of this data.
  • Basic computer skills, including the use of HMIs and other computer terminals used to monitor equipment status, document production activities, the capability to learn in more detail.
  • Excellent documentation skills.
  • Proven team work skills in working closely with an operational team in the setup, running, and changeover of a manufacturing line.
  • Responsible for maintaining a safe work environment, working safely, and accountable for supporting all Health and Safety Corporate and site goals.

Education Requirements:

  • High school diploma or equivalent.

Other Information:

  • Some of the products in Parenteral Operations are known allergens, and consequently, a post offer allergy exam may be required.
  • Ability to wear safety equipment (safety glasses, safety shoes, protective gloves, etc).
  • Must be willing to work overtime, weekends, and off shifts when required.

Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form ( ) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.

Lilly is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status.

Our employee resource groups (ERGs) offer strong support networks for their members and help our company develop talented individuals for future leadership roles. Our current groups include: Africa, Middle East, Central Asia Network, African American Network, Chinese Culture Network, Early Career Professionals, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinos at Lilly, PRIDE (LGBTQ + Allies), Veterans Leadership Network, Women's Network, Working and Living with Disabilities. Learn more about all of our groups.

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