TSMS- Scientist, Downstream
About The Position
At Lilly, the work is demanding because patients are waiting. We unite caring with discovery to help make life better for people around the world, knowing that every decision, every detail, and every day matters. Headquartered in Indianapolis, Indiana, our over 50,000 employees around the globe take on complex challenges to discover and deliver life-changing medicines, strengthen how health is understood and managed, and support the communities we serve. This is hard, urgent, selfless work—but it’s work worth doing. If you’re driven by purpose and ready to bring your best to work that truly matters for patients, we invite you to join us. Scientist Downstream - Technical Services/Manufacturing Sciences (TS/MS) As our biologics pipeline continues to expand, Eli Lilly & Company has invested in a state-of-the-art new facility in Richmond, VA. To support this exciting new GMP manufacturing facility and ensure a safe and successful start-up, we are seeking talented individuals to contribute to establishing Lilly Richmond as a reliable supplier of our innovative medicines and furthering our goal of making a difference to people’s lives. The TS/MS Downstream Scientist will provide technical support for introducing and supporting upstream downstream purification processes from startup through to routine operations. This role will provide technical expertise for the laboratory startup activities including facility design, instrument procurement and qualification in supporting downstream operations. The successful applicant will have technical expertise in laboratory scale models for downstream operations and demonstrate strong data-driven problem-solving capabilities. They will work to continuously improve process efficiency by implementing new technologies and process improvements, in addition to supporting investigation. This role will leverage data analytics, process analytical technology (PAT), and laboratory-scale models, to drive process improvement for the new facility.
Requirements
- BS in Biochemistry, Biology, Biotechnology, Chemical Engineering or related discipline
- A minimum of 2 years of experience within the biopharmaceutical industry
- 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 visas for this role, including but not limited to F-1 CPT, F-1 OPT, F-1 STEM OPT, J-1, H-1B, TN, O-1, E-3, H-1B1, or L-1.
Nice To Haves
- MSc in Biochemistry, Biology, Biotechnology, Chemical Engineering or related discipline
- Demonstrated technical capability with high productivity
- Self-starter with high initiative and data-driven approach to problem-solving
- Demonstrated strong interpersonal skills
- Demonstrated strong verbal and written communication skills
- Demonstrated adaptability and flexibility to working in different environments and teams.
Responsibilities
- Experience in supporting downstream manufacturing and associated laboratory models.
- Expertise in laboratory scale equipment operation and trouble shooting.
- Understand purpose and capability of each upstream unit operation and the impact of equipment on the process.
- Understand molecule-specific control strategy and basis of specifications and critical quality attributes.
- Work with the network and development organizations to ensure a well-understood, robust and fit-for-purpose laboratory models are developed and transferred.
- Experience with chromatographic separations and tangential flow filtration
- Leading laboratory investigations in support of production operations.
- Support the design and start-up of the laboratory including equipment configuration and purchase, development of the laboratory data management strategy, establishment of laboratory protocols
- Establish partnerships to enable cross functional work with the quality control laboratory and other Lilly sites to ensure facility startup objectives are met.
- Understand basic statistical methodologies and engage with statisticians on dada analysis
- Support process improvement initiatives and their implementation.
- Author scientific reports and technical documentation
- Understand and ensure compliance with safety, compliance, and regulatory expectations
Benefits
- company bonus (depending, in part, on company and individual performance)
- company-sponsored 401(k)
- pension
- vacation benefits
- medical benefits
- dental benefits
- vision benefits
- prescription drug benefits
- flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts)
- life insurance
- death benefits
- certain time off and leave of absence benefits
- well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities)
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
