Sr. Scientist Technical Services/manufacturing Science Api - em

Job Opportunity At Lilly

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 team works 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.

Join the energetic and growing Active Pharmaceutical Ingredient - External Manufacturing Organization (API-EM) that delivers a diverse portfolio of medicines essential to our patients around the world. The API-EM TS/MS (Technical Services / Manufacturing Science) Scientist will provide technical and scientific expertise within a dynamic external manufacturing environment. The Scientist is responsible for providing technical support to achieve the reliable and compliant manufacture of API drug substance at external contract manufacturing groups to predetermined global quality standards. This person interacts daily with a wide variety of people, primarily external partners, team members, and site management. The candidate will be responsible for supporting ongoing manufacturing at our External Partners through tasks such as process monitoring, response to issues, and improvements where necessary. A strong understanding of manufacturing principles and Lilly systems is required to ensure those same standards are applied to the external contract manufacturers. This is a Large Molecule (mAb) position. The position requires knowledge of cGMPs, applicable global regulatory manufacturing guidance, and the corporate/industry standards. The position requires working cross-functionally within the site and other functions to deliver on technical objectives.

Responsibilities include:

• Providing technical oversight for monoclonal antibody manufacturing processes
• Leading resolution of technical issues including those related to control strategy and manufacturing
• Employ excellent communication skills to manage internal and external relationships
• Building and maintaining relationships with development and central technical organizations
• Ensuring proper characterization of processes and products and ensuring effective documentation of the process description, measures, acceptable ranges, and specifications
• Ensuring that processes are compliant, capable, in control, and maintained in a validated or qualified state
• Understanding, justifying and documenting the state of validation with data that evaluate the capability of the manufacturing process to meet its stated purpose
• Influencing and implementing the network technical agenda and driving continuous improvement
• Maintaining mAb processes in a state of compliance with US and global regulations
• Understanding the scientific principles required for manufacturing intermediates and drug substances

Basic requirements include:

• Bachelors in scientific disciplines of Biotech, Chemistry, Biochemistry, Biology, Pharmacy, or Engineering (Biotech/Biochemistry strongly preferred)
• 3+ years of demonstrated hands on working experience and proficiency with pharmaceutical manufacturing and working knowledge of regulatory expectations

Additional preferences include:

• Strong understanding of regulatory requirements and their application in a manufacturing environment
• Proficient in data management practices across manufacturing operations
• Demonstrates adaptability, a collaborative mindset, and a positive attitude toward change
• Proven ability to effectively communicate and influence across diverse technical and business teams
• Skilled in managing and delivering complex, cross-functional initiatives
• Demonstrated project management expertise with a track record of coordinating and executing multifaceted projects

Some travel (<25%) is required and some off-shift work (night/weekend) may be required to support 24/7 operations. This position is located onsite in Indianapolis, IN and is not approved for remote work. Relocation will be provided.

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.

Actual compensation will depend on a candidate's education, experience, skills, and geographic location. The anticipated wage for this position is $66,000 - $171,600. Full-time equivalent employees also will be eligible for a company bonus and a comprehensive benefit program.