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.
Responsible for maintaining a safe work environment, working safely, and accountable for supporting all Health and Safety Corporate and site goals.
Must be willing to work overtime, weekends, and off shifts when required.
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, 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
Additional Skills/Preferences:
Experience with GMP
Ability to work through production issues including basic troubleshooting skills, and use of tools.
PMX, Master Control, Flow-stream, SAP 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 teamwork skills in working closely with an operational team in the setup, running, and changeover of a manufacturing line
Additional Information:
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%)
Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color
Benefits
Health insurance
Additional Information
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.
The Operator - Visual Inspection will work in the Kenosha County 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.
Eli Lilly · Pleasant Prairie WI