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Lilly Device Assembly Manufacturing Operator - Day Shift in Research Triangle Park, North Carolina

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 35,000 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.

Lilly has designed a new Parenteral, Device Assembly, and Packaging Facility in Raleigh-Durham, North Carolina. This is an exciting opportunity to help build a state-of-the-art facility and Quality System from the ground up.

The Manufacturing Operator will work in the RTP Device Assembly, where Lilly autoinjector devices are assembled and packaged. Operators will be responsible for the safe operation of highly automated equipment producing products of the highest quality for Lilly patients, with Safety First and Quality Always.

Key Objectives/Deliverables:

  • Adhere to RTP Plant safety policies and procedures, contribute to a safe work environment.

  • Setup and operate highly automated equipment in the Device Assembly Area.

  • Adhere to standard operating procedures and current Good Manufacturing Practices to ensure quality of product.

  • Document process steps on appropriate batch documentation (Electronic Ticket, SAP, Cleanings, etc.).

  • 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 activities and reporting issues to supervision.

  • Contribute to the achievement of key departmental objectives including improving safety performance, reducing deviations, improving productivity, and training compliance.

  • Must be willing to work 12 hour shifts (2-2-3 schedule)

  • Currently in the start up phase of operations. Candidate must be flexible and be willing to perform non-routine work with Safety & Integrity in mind at all times

Minimum Qualifications:

  • Entry Level with some experience working in a GMP environment preferably in a pharmaceutical industry.

  • Willing to learn and be open-minded

  • Strong potential to multitask

  • Strong ability to demonstrate attention to detail

  • Strong integrity

Education Requirements:

  • High School Diploma/GED required

Eli Lilly and Company, Lilly USA, LLC and our wholly owned subsidiaries (collectively “Lilly”) are committed to help individuals with disabilities to participate in the workforce and ensure equal opportunity to compete for jobs. If you require an accommodation to submit a resume for positions at Lilly, please email Lilly Human Resources ( ) for further assistance. Please note This email address is intended for use only to request an accommodation as part of the application process. 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.

As a condition of employment with Eli Lilly and Company and its subsidiaries in the United States and Puerto Rico, you must be fully COVID-19 vaccinated and provide proof of vaccination satisfactory to the company (subject to applicable law).