Eli Lilly and Company

Scientist-TS/MS


PayCompetitive
LocationCarolina/Puerto Rico
Employment typeFull-Time

This job is now closed

  • Job Description

      Req#: R-53894

      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.

      We are seeking a hardworking post-doctoral scientist with outstanding research skills to contribute to research projects at Lilly. This role will focus on the process development/continuous improvement of the purification process of an E coli derived fast-acting insulin analog. If you are a passionate multidisciplinary scientist, consider applying to this exciting role!

      Process Development Scientist is a fixed term position post-doctoral assignment intended to support technical operations at Eli Lilly’s state of the arts PR05 Insulin Manufacturing Facility located in Carolina, Puerto Rico. The position will provide technical and scientific leadership to support the technical agenda through the design and execution of experiments that exploit the usage of laboratory models for the continuous improvement of the purification process. We're looking for a self-directed and highly motivated individual who wants to learn new techniques while continually pursuing research and publication goals.

      RESPONSIBILITIES:

      The post-doctoral Process Development Scientist will be responsible for: Playing a leadership role in the design of experiments, and the development and usage of laboratory models suitable for optimizing Insulin purification operations; promoting deep technical excellence and scientific understanding throughout the TS/MS organization; driving and prioritizing productivity improvements through bench scale experimentation; ensuring successful technical transfers and providing technical support for the purification process; partnering and networking with the Indianapolis and PR TS/MS organization and the multidisciplinary Process Team to troubleshoot and improve the capability of purification processes; executing with good documentation and laboratory practices; and promoting and modeling by example compliance to GLPs, health, safety and environmental regulations.

      During the experience, you will be able to:

      • Gain hands-on experience on the operation of equipment and instrumentation used for the modeling of commercial protein purification processes.
      • Solidify analytical skills on U/HPLC technologies, pharmaceutical data handling and process analytic applications.
      • Interact with multidisciplinary teams supporting manufacturing operations and familiarize yourself with career opportunities for professionals sharing your background in our manufacturing organization.
      • Expand your experience based to enhance your competitiveness in the pharmaceutical job market.

      Basic Qualifications

      PhD in a life science related field (Biochemistry, Chemistry, Biology, Biotechnology, Chemical Engineering or Bioengineering).

      Experience: Research experience using laboratory scale chromatographic and filtration systems is preferred. Demonstrated strong scientific and technical knowledge in protein purification, protein characterization and material characterization techniques, statistical data analysis, technical writing and project management.

      Other Requirements:

      • Computer literate
      • Teamwork oriented
      • Bilingual (English/Spanish)
      • Strong communication skills and the ability to collaborate with other parts of the organization and across multiple levels are essential
      • Compliance mindset and sound judgment
      • Flexibility is required to provide technical support and continuity to a 24/7 process operation
      • Candidate must also be willing to travel

      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 ( Lilly_Recruiting_Compliance@lists.lilly.com ) 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.

      Our employee resource groups (ERGs) offer strong support networks for their members and help our company develop talented individuals for future leadership roles. Our current groups include: Africa, Middle East, Central Asia Network, African American Network, Chinese Culture Network, Early Career Professionals, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinos at Lilly, PRIDE (LGBTQ + Allies), Veterans Leadership Network, Women’s Network, Working and Living with Disabilities. Learn more about all of our groups.

      #WeAreLilly

  • About the company

      Eli Lilly and Company is an American pharmaceutical company headquartered in Indianapolis, Indiana, with offices in 18 countries.