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.

EDUCATIONAL REQUIREMENTS:

• Minimum of a B.S. in Chemistry, Engineering, Pharmacy, Pharmaceutical Sciences, or similar scientific field
• Preference of 5+ years in GMP Drug Product Manufacturing, External Manufacturing, Formulation Development or other related function.

ADDITIONAL INFORMATION/REQUIREMENTS:

• Some domestic and/or international travel required (< 10%)
  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 (https://careers.lilly.com/us/en/workplace-accommodation) 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 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.
  

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• The CT Manufacturing Technical Representative (Tech Rep) must demonstrate the technical ability to plan and perform cGMP activities for drug product manufacturing. These activities include batch record preparation, oversight of manufacturing execution, sample submission, and batch record review and disposition with Quality for multiple types of manufactures.
• The CT Manufacturing Technical Representative partners with Development Scientists, Third Parties and other Lilly groups (e.g., CT Packaging, Regulatory, Quality Assurance, Analytical, Project Management, and Commercial Manufacturing) to enable the manufacturing and delivery of drug product and technical information deliverables. Additionally, the Technical Representative works closely with the CT Manufacturing Operations group to enable planning, scheduling, material movement, budget development and testing.