Lilly

Healthcare

AssociateScientist-ProcessDevelopment

$71–187k Boston, Massachusetts, United States FULL TIME
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Mid+ candidates.

The Brief

“Associate Scientist - Process Development at Lilly. Skills: Downstream purification, Viral vector programs, Process development. Lead development, optimization, and scale-up of downstream purification. Design and implement purification strategies using Iodixanol and”

Industry & Context.

Healthcare
Problems you'll solve

Troubleshooting; Process characterization; Process robustness studies; Data analysis; Result interpretation

What They're Looking For.

Must Have

Master's degree in biology, biochemistry, chemical engineering, biotechnology or related field, 8+ years of relevant downstream process development experience in industry, Authorized to work in the United States on a full-time basis

Nice to Have

CsCl and iodixanol ultracentrifugation, Affinity chromatography, Ion-exchange chromatography, TFF/UFDF operations including concentration, diafiltration, and formulation development, AKTA systems and Unicorn software, Process scale-up, platform development, and purification process characterization, Analyzing purification performance and product quality attributes using relevant analytical methods, AAV downstream process development and capsid enrichment workflows, Automated chromatography systems and process intensification strategies, Supporting technology transfer and manufacturing readiness activities, Familiarity with GMP development environments and regulatory expectations

What You'll Do.

and scale-up of downstream purification

Design and implement purification strategies using Iodixanol and

Design and implement affinity chromatography

Design and implement ion-exchange chromatography (AEX/CEX)

Design and implement membrane chromatography

Design and implement polishing operations

Lead AKTA-based chromatography workflow development

Lead process intensification initiatives

Develop scalable downstream platform approaches

Support rapid material generation

Support process consistency across programs

Independently design experiments

Present technical conclusions to multi-functional teams and leadership

Drive troubleshooting

Drive process characterization

Drive process robustness studies

Collaborate closely with upstream

Support program deliverables and timelines

Support technology transfer

Support process documentation

Support development reports

Lead development and optimization of TFF/UFDF workflows

Optimize workflows for concentration

Optimize workflows for buffer exchange

Optimize workflows for formulation

Optimize workflows for process scalability

Mentor junior scientists/engineers

Provide technical guidance across purification activities

Contribute to implementation of new purification technologies

Contribute to implementation of automation tools

Contribute to implementation of continuous process improvements

Ensure compliance with safety standards

Ensure compliance with documentation standards

Ensure compliance with quality standards

How You'll Work.

Team & Collaboration

Multi-functional teams; Upstream, analytical, manufacturing; External partners

Communication Scope

Present technical conclusions

Process & Methodology

Process development strategies, Platform development initiatives, Technology implementation

Full Job Description

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 highly motivated Principal Engineer to join the Downstream Process Development team. The successful candidate will lead development and optimization of downstream purification processes supporting viral vector programs from research through preclinical development. The ideal candidate will possess deep technical expertise in downstream purification technologies including ultracentrifugation, chromatography, and tangential flow filtration (TFF), with demonstrated experience driving process development strategies, platform development initiatives, technology implementation, and multi-functional collaboration. This role requires strong scientific leadership, hands-on technical capability, and the ability to independently lead complex purification development activities in a fast-paced environment. **Key Responsibilities** * Lead development, optimization, and scale-up of downstream purification workflows for viral vectors. * Design and implement purification strategieusingng Iodixanol and CsCl density gradient ultracentrifugation, affinity chromatography, ion-exchange chromatography (AEX/CEX), membrane chromatography, and polishing operations. * Lead AKTA-based chromatography workflow development and process intensification initiatives. * Develop scalable downstream platform approaches to support rapid material generation and process consistency across programs. * Independently design experiments, analyze data, i

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