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.

BASIC QUALIFICATIONS

• Bachelor’s Degree or higher in science or science related field such as Pharmacy, Chemistry, Engineering, Biological Science, or related Life Sciences.
• Experience with DP manufacturing technologies/processes.
• Experience with DP technical transfers and commercialization of new drug products.
• Experience with qualification of DP manufacturing equipment, utility, and facility.
• Self-management and organizational skills to produce quality deliverables within established time frames.
• Demonstrated ability of collaboration to operate cross functionally and hold technical/process discussions with third parties.
• A thorough understanding of cGMPs.
  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.
  

  WeAreLill

The TSMS Representative of Drug Products External Manufacturing (DPEM) Commercialization is responsible for providing technical support to commercialization activities within DPEM. DPEM is responsible for the commercialization of drug products (DPs) at selected contract manufacturers (CMs) located globally.
The scope of the role includes technical support for all commercialization assets. A key part of this role is supporting each commercialization project to ensure consistency in approach and processes, up through and including submission.
The DPEM TSMS Commercialization Representative is also responsible for providing process oversight, according to the product control strategy and governing documentation, to ensure the appropriate handover to the commercial manufacturing unit.