Lilly Medicine Foundry
Pharmaceutical
ProcessEngineer,Purification
Neural analysis suggests this role is
optimal for Mid+ candidates.
“Process Engineer, Purification at Lilly Medicine Foundry. Skills: Process Engineer, Purification, API manufacturing, biologics, peptides, oligonucleotides, bioconjugates. Perform impact and risk assessments for the relevant equipment (chromatography skids/columns, TFF skids, etc. ) and unit operations. Learn the lab and plant design for the purification equipment including automation recipes and procedures”
Industry & Context.
analytical and problem-solving skills
What They're Looking For.
Must Have
BS or MS in chemical engineering or related discipline, minimum of 1-4 years of experience with a pharmaceutical, biotech, or CMO environment supporting the process engineering of drug substance active pharmaceutical ingredient (API) manufacturing or development, Qualified applicants must be authorized to work in the United States on a full-time basis
Nice to Have
Deep technical interest and understanding in the field of Chemical Engineering, Ability to work well in a team environment incorporating a variety of functional relationships and desire to be point of accountability, Experience with any of the following software packages: DeltaV, OSI-PI, Dynochem, Aspen, and/or electronic lab notebooks, analytical and problem-solving skills, oral and written communication skills for a diverse audience, e. g. , both operations staff and management, Ability to work on own initiative and as part of a Process Team consisting of a diverse group of management, production, science and engineering professionals, Understanding of process control systems, Creativity to identify improvement opportunities and the tenacity/initiative to see them implemented, Guidance/mentoring of others through processes, Flexibility to meet business needs
What You'll Do.
Perform impact and risk assessments for the relevant equipment (chromatography skids/columns
etc. ) and unit operations
Learn the lab and plant design for the purification equipment including automation recipes and procedures
Ensure that people and their environment are safe and that company policies concerning safety are followed
Ensure processing equipment remains compliant with internal Quality System requirements
applicable engineering standards
and cGMP requirements
Assesses rig fit by receiving the technical data package for new processes and performing modeling
simulations and/or experimental work as required to ensure heat and mass transfer are acceptable when scaling to the plant
or approve high-quality technical reports and regulatory submissions dealing with the work performed by the department
Ensure that records and technical notebooks are adequately maintained
Develop or review plans and timetables for project work
How You'll Work.
Team & Collaboration
Active engagement and communication with: HSE, Quality Assurance, Tech Services, Development, Operations, FUME/C&Q, Automation, Maintenance, Environmental Monitoring, and Manufacturing; Ability to work well in a team environment incorporating a variety of functional relationships; Ability to work as part of a Process Team consisting of a diverse group of management, production, science and engineering professionals
Communication Scope
oral and written communication skills for a diverse audience, e. g. , both operations staff and management
Process & Methodology
Develop or review plans and timetables for project work
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. **About the Lilly Medicine Foundry:** Lilly recently announced a $4.5 billion investment to create the Lilly Medicine Foundry, a new center for advanced manufacturing and drug development. The first-ever facility of its kind, combining research and manufacturing in a single location, the Medicine Foundry will allow Lilly to further develop innovative solutions to optimize manufacturing processes and increase capacity for clinical trial medicines, while also reducing costs and environmental impact. **Organizational Overview:** Lilly is currently constructing an advanced research facility for production of API molecules for clinical trials located in Lebanon, IN. This facility is Lilly’s largest investment in a clinical trial manufacturing capacity and is intended to provide APIs for current and future products, including new modalities. This is a unique opportunity to be a part of the startup team for a greenfield manufacturing site, and the successful candidate will help to build the processes and facility to enable a successful startup into GMP manufacturing operations. We are seeking experienced Process Engineers to support purification of biologics, peptides, oligonucleotides, and bioconjugates. This position involves solving technical challenges with equipment design, developing and sustaining process knowledge, optimizing processes, and managing equipment capabilities. **Responsibilities** The Process Engineer provides te
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