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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 39,000 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 will work in the Indianapolis Parenteral Manufacturing site in the Parenteral Device Assembly and Packaging plant where Parenteral products for domestic and international markets are assembled and packaged. The primary purpose of the job is to assemble and package device products.
Adhere to Parenteral Site safety policies and procedures and contribute to a safe work environment
Setup and operations of equipment in assembly, labeling, and packaging areas
Adhere to standard operating procedures and current Good Manufacturing Practices to ensure quality of product
Document process steps on appropriate batch documentation
Attain and maintain qualification for the operation of assigned process equipment and duties in the area
Identify opportunities for operational improvements
Proactively monitor documentation and product quality, properly documenting all activity and reporting issues to supervision
High school diploma/GED
Completion of Post Offer Exam, Completion of Work Simulation or Completion of Administrative Skills Testing if applicable
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
Ability to demonstrate attention to detail
Basic math skills
Basic computer skills, with the capability to learn in more detail
Excellent documentation skills
Responsible for maintaining a safe work environment, working safely and accountable for supporting all HSE Corporate and Site Goals
Experience with cGMP environment
Strong ability to multi task
Good verbal and written communication skills
Curiosity and technical abilities/troubleshooting
This position is not permanent. It is for a fixed duration of two years with potential to extend annually for up to 4 years
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
Detail requirement and what we offer
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