Global Product Steward - Genetic Medicines

Location: Indianapolis

Advisor Parenteral Global Product Steward - Genetic Medicines page is loaded## Advisor Parenteral Global Product Steward - Genetic Medicines locations:
US, Indianapolis INtime type:
Full time posted on:
Posted Todayjob requisition :
R-105669

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  this individual contributor position Global Product Steward scientist role, you will have the opportunity to collaborate with cross functional teams across Lilly and external manufacturing organizations. As an individual contributor, you will work side-by-side with other Lilly professionals to drive the drug product technical agenda, including the exciting journey of new pipeline products from development into manufacturing.
*
* Key Responsibilities:

*** Provide technical stewardship of parenteral drug products and genetic medicines.
* Collaborate with cross-functional team to support global parenteral manufacturing sites for new product commercialization, process improvements and technology transfers at internal and external manufacturing sites.
* Collaborate with process engineers and development scientists to design and transfer robust manufacturing processes to commercial and third-party manufacturing operations. This includes serving as a liaison to CM&C teams to shepherd new pipeline products from development into manufacturing.
* Leverage and influence the internal and external scientific community to impact Lilly’s ability to commercialize life-changing medicines, improve productivity, and create long-term value.
* Integrate cross-functional and/or external information and apply technical knowledge to data-driven decision-making
* Define the vision and drive advancements of technical capabilities
* Suggest and evaluate opportunities for molecule, product, and business process improvement. This includes driving the molecule/product technical agenda with a specific focus on process/productivity improvements in partnership with the global manufacturing sites.
* Act with speed, agility, and decisiveness to identify the critical issues to resolve; influences team and/or stakeholders on the critical risks and plan for resolution.
* Champion changes that increase the effectiveness of overall business objectives
* Coach and mentor junior associates.
** Basic Requirements:
*** A degree in a relevant area such as Biochemistry, Chemistry, Chemical Engineering, Biology, or Pharmaceutical Science with one of the following:
* PhD degree in above discipline with a minimum of 5 years of practical experience in parenteral product manufacturing or
* Master’s degree with a minimum of 10 years of practical experience in parenteral product manufacturing or
* Bachelor’s degree with a minimum of 15 years of practical experience in parenteral product manufacturing
** Additional Skills/Preferences:
*** Proficient in biomolecule, genetic medicine characterization and product development with substantial experience in GMP manufacturing.
* Demonstrated ability to analyze and interpret complex technical data and troubleshoot data issues.
* Demonstrated examples of leadership, influence, and problem-solving skills.
** Additional Information:
*** Domestic/international travel: 10-25 %
Qualified applicants must be authorized to work in the United States on a full-time basis. Lilly will not provide support for or sponsor work authorization and/or visas for this role.

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