Senior Scientist – Manufacturing Science in Indianapolis

Job Description

Join American pharmaceutical leader Eli Lilly and Company, currently hiring Senior Scientist – Manufacturing Science in Indianapolis, Apply Lilly careers in Indianapolis Indiana.

 

Position : Senior Scientist – Manufacturing Science

Location : Indianapolis, Indiana

Job id: R-34389

 

Job Details

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.Organization Overview: The mission of Technical Services/Manufacturing Science (TS/MS) is to provide scientific leadership and technical support for manufacturing to make medicine today and tomorrow.  The Parenteral drug product network TSMS provides product stewardship for all parenteral products across multiple manufacturing sites.Responsibilities: In this 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.Provide technical stewardship of parenteral drug products.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.Design and execute necessary laboratory and pilot studies, as well as prepare technical reports and/or regulatory submissions to support business objectives.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 Parenteral Product Network global manufacturing sites.Coach and mentor junior associates.Basic Requirements:  – A degree in relevant area such as Biochemistry, Chemistry, Chemical Engineering, Biology or Pharmaceutical Science with one of the following:PhD degree with 5  years of practical experience of parenteral product manufacturing orMaster degree with 10 years of practical experience of parenteral product manufacturing orBachelor degree with 15 years of practical experience of parenteral product manufacturingAdditional Skills/Preferences:Demonstrated examples of leadership, influence, and problem solving skills.Demonstrated ability to analyze and interpret complex technical data and troubleshoot data issues.Strong written and oral communication skills.Preparation, review and response preparation of global regulatory submissions i.e. BLAs and NDAs and other technical communications.Ability to Leadership teams to successfully deliver projects on time and in scope.Working knowledge of statistical design of experiments and analysis.Working knowledge and scientific understanding of product distribution, drug delivery devices and advanced drug delivery systems.Proficient in biomolecule characterization and product development with substantial experience in GMP manufacturing.Additional Information:Recognition and future promotion on the Technical Ladder10-20% domestic and international travelLilly 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 statusEli 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.

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).

 

 

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