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Mansueto Ventures is home to two of the most iconic and vibrant brands in business publishing: Inc. and Fast Company. Every day, the content, awards, and events produced help entrepreneurs and innovators succeed by providing useful insights, sparking essential conversations, and offering much-needed inspiration.

Inc. is the voice of the American entrepreneur, inspiring and documenting the risk-takers and ultra-driven go-getters who represent the most dynamic force in the American economy.
Fast Company is the world’s leading business media brand, focusing on innovation in technology, leadership, and design to inspire readers to shape the future of business.

","New York, NY","coloredLogo","logoAttachment","thumbnail","thumbnailAttachment","hexCode","#080D0C","headline","Publisher of Inc. and Fast Company, empowering innovators and entrepreneurs.","/companies/mansueto-ventures-careers","hasJobSubmission","isSavedJob","similarJobs",[507,516,525,534,547],{"_426":425,"_430":508,"_449":450,"_441":442,"_240":509,"_437":510,"_424":425,"_111":511,"_428":191,"_429":191,"_451":450,"_439":440,"_422":512,"_452":453,"_427":115,"_473":474,"_457":513,"_475":514,"_476":440,"_478":479,"_480":481,"_482":515},["D",1770058800000],"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.

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.

In the Project Delivery Phase and Startup Phase of the project (2026 to 2028), roles will be fluid and dynamic as we endeavor to support the project delivery, build a new organization, develop and implement the necessary systems and business processes required to support GMP operations. This will require significant collaboration, creativity and resilience as the Lilly Medicine Foundry goes from design, to start-up, and to steady-state operations.

Position Summary

The Advisor/Sr Advisor of Project & Strategy for Analytical GMP Laboratories will lead clinical manufacturing and analytical strategy for GMP testing laboratories at the Lilly Medicine Foundry. This role drives phase-appropriate, risk-based analytical strategies from development through GMP execution, oversees strategic planning across CMC analytical deliverables, and partners cross-functionally to align analytical strategy with compliance, capability build, and digital enablement.

Key Responsibilities

Strategic Leadership & Analytical Planning

Define and lead phase-appropriate, risk-based analytical strategies to support clinical manufacturing.

Develop integrated method readiness strategies, including validation and transfer across multiple modalities.

Oversee CMC analytical activities, specifications, stability strategies, and lifecycle elements.

Digital Enablement & Technology Advancement

Support digitalization initiatives and implementation of new technologies to enhance analytical workflows.

Drive adoption of PAT, automation, and high-throughput approaches for efficiency and compliance.

Continuous Improvement & Lifecycle Management

Champion continuous improvement initiatives and analytical lifecycle performance metrics.

Ensure alignment with GMP, ICH guidance, and regulatory frameworks throughout the product lifecycle.

Cross-Functional Collaboration

Partner with QA, QC, Manufacturing, Engineering, and R&D to ensure analytical strategies support clinical and commercial objectives.

Act as a key liaison for technology transfer and method strategy across Foundry operations.

Minimum Qualifications

MS or PhD in Chemistry, Biochemistry, Pharmaceutical Sciences, or related discipline.

10+ years of experience in analytical development, GMP laboratories, or CMC functions.

Strong understanding of ICH guidance, GMP principles, lifecycle management, and regulatory frameworks.

Additional Skills and Preferences

Proven cross-functional leadership experience.

Experience across synthetic and biological modalities.

Familiarity with PAT, automation, and high-throughput workflows.

Continuous improvement mindset with demonstrated CI experience.

Strong strategic thinking, influence, and stakeholder management skills.

Other Information:

Initial location at Lilly Technology Center, Indianapolis.

Permanent location at the new Lilly Medicine Foundry in Lebanon, Indiana.

Flexibility to work from Indianapolis (or other Lilly sites) may be required throughout 2026 and 2027.

Position requires on-site presence, 8-hour days, five days per week, with flexibility to support activities during shutdowns, weekends, etc.

0-10% travel required.

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 (https://careers.lilly.com/us/en/workplace-accommodation) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.

Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status.

Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ+ Allies), Veterans Leadership Network (VLN), Women's Initiative for Leading at Lilly (WILL), enAble (for people with disabilities). Learn more about all of our groups.

Actual compensation will depend on a candidate's education, experience, skills, and geographic location. The anticipated wage for this position is\n$126,000 - $204,600

Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly's compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees.

#WeAreLilly\n","At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indian...","Advisor Projects & Strategy Analytical GMP Laboratories Lilly Medicine Foundry",["B","2408828544"],"/jobs/2408828544-advisor-projects-strategy-analytical-gmp-laboratories-lilly-medicine-foundry","Advisor Projects & Strategy Analytical GMP Laboratories Lilly Med...","/jobs?keyword=Advisor+Projects+%26+Strategy+Analytical+GMP+Laboratories+Lilly+Med...",{"_426":425,"_430":517,"_449":450,"_441":518,"_240":519,"_437":510,"_424":425,"_111":511,"_428":191,"_429":191,"_451":450,"_439":440,"_422":520,"_452":521,"_427":115,"_473":522,"_457":523,"_475":514,"_476":440,"_478":524,"_480":481,"_482":515},["D",1769968800000],"Eli Lilly and","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.\nLilly 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.\nIn the Project Delivery Phase and Startup Phase of the project (2026 to 2028), roles will be fluid and dynamic as we endeavor to support the project delivery, build a new organization, develop and implement the necessary systems and business processes required to support GMP operations. This will require significant collaboration, creativity and resilience as the Lilly Medicine Foundry goes from design, to start‑up, and to steady‑state operations.\nPosition Summary

The Advisor/Sr Advisor of Project & Strategy for Analytical GMP Laboratories will lead clinical manufacturing and analytical strategy for GMP testing laboratories at the Lilly Medicine Foundry. This role drives phase‑appropriate, risk‑based analytical strategies from development through GMP execution, oversees strategic planning across CMC analytical deliverables, and partners cross‑functionally to align analytical strategy with compliance, capability build, and digital enablement.\nKey Responsibilities

Strategic Leadership & Analytical Planning

Define and lead phase‑appropriate, risk‑based analytical strategies to support clinical manufacturing.\nDevelop integrated method readiness strategies, including validation and transfer across multiple modalities.\nOversee CMC analytical activities, specifications, stability strategies, and lifecycle elements.\nDigital Enablement & Technology Advancement

Support digitalization initiatives and implementation of new technologies to enhance analytical workflows.\nDrive adoption of PAT, automation, and high‑throughput approaches for efficiency and compliance.\nContinuous Improvement & Lifecycle Management

Champion continuous improvement initiatives and analytical lifecycle performance metrics.\nEnsure alignment with GMP, ICH guidance, and regulatory frameworks throughout the product lifecycle.\nCross‑Functional Collaboration

Partner with QA, QC, Manufacturing, Engineering, and R&D to ensure analytical strategies support clinical and commercial objectives.\nAct as a key liaison for technology transfer and method strategy across Foundry operations.\nMinimum Qualifications

MS or PhD in Chemistry, Biochemistry, Pharmaceutical Sciences, or related discipline.\n10+ years of experience in analytical development, GMP laboratories, or CMC functions.\nStrong understanding of ICH guidance, GMP principles, lifecycle management, and regulatory frameworks.\nAdditional Skills and Preferences

Proven cross‑functional leadership experience.\nExperience across synthetic and biological modalities.\nFamiliarity with PAT, automation, and high‑throughput workflows.\nContinuous improvement mindset with demonstrated CI experience.\nStrong strategic thinking, influence, and stakeholder management skills.\nOther Information

Initial location at Lilly Technology Center, Indianapolis.\nPermanent location at the new Lilly Medicine Foundry in Lebanon, Indiana.\nFlexibility to work from Indianapolis (or other Lilly sites) may be required throughout 2026 and 2027.\nPosition requires on‑site presence, 8‑hour days, five days per week, with flexibility to support activities during shutdowns, weekends, etc.\n0‑10% travel required.\nLilly 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 (https://careers.lilly.com/us/en/workplace-accommodation) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.\nLilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status.\nOur employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ+ Allies), Veterans Leadership Network (VLN), Women’s Initiative for Leading at Lilly (WILL), enAble (for people with disabilities). Learn more about all of our groups.\nActual compensation will depend on a candidate’s education, experience, skills, and geographic location. The anticipated wage for this position is $126,000 – $204,600.\nFull‑time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company‑sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well‑being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities). Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly’s compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees.\n#WeAreLilly

#J-18808-Ljbffr\n",["B","2394144343"],"Work at Eli Lilly and","5 days ago","/jobs/2394144343-advisor-projects-strategy-analytical-gmp-laboratories-lilly-medicine-foundry","/jobs?keyword=Eli+Lilly+and",{"_426":425,"_430":526,"_449":450,"_441":442,"_240":527,"_437":510,"_424":425,"_111":528,"_428":191,"_429":191,"_451":450,"_439":440,"_422":529,"_452":453,"_427":115,"_473":530,"_457":531,"_475":532,"_476":440,"_478":479,"_480":481,"_482":533},["D",1770397200000],"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.

Organization and Position Overview:

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.

The Associate Director - Biologics Operations is directly responsible for managing the day-to-day manufacturing operations in the Biologics building and provides oversight for the operational resources assigned to the execution team. The role is responsible for the leadership of frontline leaders in direct execution of manufacturing instructions (e.g., batch production record, SOP's, etc.) to safely and compliantly manufacture high-quality medicine. The role serves as the key integrator of the cross-functional team to drive safety, quality, and continuous improvement in pursuit of Operational Excellence. The Associate Director - Biologics Operations provides leadership, acts as a key integrator, has accountability for the cross functional execution team, and ensures that appropriate staffing is in place.

In the project delivery phase and startup phase of the project (startup expected 2025 to 2028), leadership roles will be fluid and dynamic as we endeavor to support the project delivery, build a new organization, develop and implement the necessary systems and business processes required to support GMP operations, and build the site culture. This will require significant collaboration, creativity and resilience as the site grows to a full scale GMP manufacturing through start up.

Key Responsibilities:

Build and promote a strong Safety and Quality culture. Maintain a safe working environment and conduct production activities in a manner that protects safety, environment and quality.\nEnsure consistency of operations across shifts through active engagement on the production floor.\nOwn the implementation of the change and improvement agenda for the assigned area, ensuring cross functional support and integration.\nSet objectives and development plans for Operations staff, including Operations Leaders and Operators.\nManage events as required, ensuring appropriate communication within the team and with external teams. Provide input and approve investigations.\nEnsure that team members are appropriately trained, and that operating procedures and training material are available and current.\nEnsure regulatory compliance and operational excellence by supporting lean principles.\nParticipate in development and delivery of the medium- and long-term strategic direction for the site.\nEnsure Biologics operations remain compliant with all applicable regulatory requirements. (e.g. Safety, Quality/cGMP, Environmental, Financial, Legal, HR.)\nSupport site governance through participation, influence and leadership in cross functional meetings and initiatives.\nSpecifically, during the startup phase of the Lilly Medicine Foundry (2025 to 2027) leadership will be expected to be collaborative, inclusive, and support the broader team to:

Attract, hire and onboard a significant number of top talent to the Foundry team establishing the right attitude, curiosity and learning agility to deliver on the Foundry mission.\nBuild the organization with the necessary capability, capacity and culture to operate this facility to the highest standards of safety, quality, and operational excellence.\nDevelop and implement the systems and processes needed to run the site, leveraging existing Lilly knowledge where necessary, but also incorporating external learning.\nAbility to work with a team, make independent decisions, and influence diverse groups.\nSupport the project team to deliver the facility to you as the end user, by providing feedback and support on design decisions, commissioning strategies etc. Collaborate with them to ensure the right decisions are made to meet project deliverables and longer-term strategic goals for the site.\nBasic Requirements:

Minimum of a bachelor's degree in a relevant scientific, engineering or operations discipline and a minimum of 5 years of experience in a leadership role managing operations or relevant experience within the pharmaceutical industry.\nAdditional Preferences:

Ability to work with a team, make independent decisions, and influence diverse groups.\nAbility to instill teamwork within the department and demonstrate key interpersonal skills.\nAbility to provide innovative solutions to plant, divisional, and corporate issues and leverage ideas from other functional areas.\nAbility to communicate verbally and in writing to various audiences, particularly one-on-one coaching and feedback with direct reports and technical process team members\nAbility to function in a cross functional team environment as a leader.\nOther Information:

Initial location at Lilly Technology Center, Indianapolis.\nPermanent location at the new Lilly Medicine Foundry in Lebanon, Indiana.

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 (https://careers.lilly.com/us/en/workplace-accommodation) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.

Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status.

Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ+ Allies), Veterans Leadership Network (VLN), Women's Initiative for Leading at Lilly (WILL), enAble (for people with disabilities). Learn more about all of our groups.

Actual compensation will depend on a candidate's education, experience, skills, and geographic location. The anticipated wage for this position is\n$123,000 - $180,400

Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly's compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees.

#WeAreLilly\n","Associate Director - Biologics Operations - Lilly Medicine Foundry",["B","2462356276"],"9 hours ago","/jobs/2462356276-associate-director-biologics-operations-lilly-medicine-foundry","Associate Director - Biologics Operations - Lilly Medicine Foundr...","/jobs?keyword=Associate+Director+-+Biologics+Operations+-+Lilly+Medicine+Foundr...",{"_426":425,"_430":535,"_449":450,"_441":536,"_240":537,"_437":538,"_424":425,"_111":539,"_428":191,"_429":191,"_451":450,"_439":440,"_422":540,"_452":541,"_427":115,"_473":542,"_457":543,"_475":544,"_476":440,"_478":545,"_480":481,"_482":546},["D",1770148800000],"Eli Lilly and Company","Overview\nAt 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.

Organization And Function Overview

Lilly recently announced a $4.5 billion investment to create the Lilly Medicine Foundry, a pioneering center that integrates advanced manufacturing and drug development. As the first facility of its kind, the Foundry is designed to accelerate innovation in manufacturing processes, expand capacity for clinical trial medicines, and speed Lilly innovative medicine to Clinics, and reduce both costs and environmental impact.

The Process Translation and Execution (PTE) team plays a critical role in this mission. PTE is responsible for leading technology transfers from lab or pilot scale to cGMP production, collaborating with Operations and cross-functional teams to ensure reliable clinical supply and right-first-time production. The team also drives continuous improvement, advances the site technical agenda, and research transformative technologies and champions the accelerated adoption of innovation in clinical and commercial manufacturing, ultimately delivering patient-centric outcomes.

We are seeking enthusiastic scientists and engineers to join the PTE team and help bring the Lilly Medicine Foundry’s vision to life.

Key Responsibilities

Process Transfer and Scale-Up: Oversee the successful transfer of API/DS processes from development to Foundry with a focus on purification and flexibility in supporting multiple modalities, including Biologics, ADCs, Tides, ensuring process fit to plant, scalability, and right-first-time execution.

Continuous Improvement: Apply scientific knowledge to troubleshoot production issues, identify areas for improvement, design and conduct lab studies, and implement new technologies or procedures.

Data Analysis and Reporting: Monitor manufacturing processes, analyze experimental and production data, and author technical reports, protocols, and change controls.

Documentation and Compliance: Support the creation and review of technical documents, batch records, process descriptions, and risk assessments, ensuring adherence to cGMP and regulatory standards.

Cross-Functional Collaboration: Work closely with various functions within Foundry and across PRD/CMC to achieve project goals and ensure product quality.

Investigations and CAPA Support: Lead or assist in process-related investigations, assess deviations, design and conduct needed lab studies, and support Corrective and Preventive Actions (CAPAs) to maintain product quality and timelines.

Technical Expertise: Provide scientific input during audits, provide on-floor support for critical operations, and mentor or supervise junior scientists or technicians in laboratory procedures, data analysis and related PTE activities.

Site Technology Agenda & Innovation: Collaborate with PRD, Process Engineering, and leverage internal/external/academic partnerships to accelerate innovation, including scouting, assessing, developing, and implementing new technologies. Collaborate with Tech Lilly and Digital Innovation to contribute to identification and implementation of transformative technologies and methodologies to accelerate technology transfer, minimize translation errors, and drive continuous improvement.

Basic Requirements

Education: BS, MS or PhD in Biology, Biochemistry, Biological Engineering, Chemical/Biochemical Engineering, or related disciplines

Experience: BS with 15+ years, or MS with 10+ years, or PhD with 4+ years in Biologics/Drug Conjugates Product/Process Development, Manufacturing Technical Services, or related functional roles

Additional Skills And Preferences

Technical Expertise: Strong knowledge of bioprocesses (upstream or downstream, including cell culture, centrifugation, filtration, chromatography, conjugation, and aseptic processing).

Problem-Solving Skills: Proven ability to analyze data, perform root cause analysis, and resolve complex technical challenges.

Communication Skills: Excellent written and verbal communication skills for technical report writing, presentations, and effective collaboration across teams.

Collaboration: Demonstrated success in cross-functional, dynamic, and matrixed environments.

Regulatory Knowledge: Solid understanding of biopharmaceutical manufacturing principles and cGMP requirements.

Scientific Curiosity: Proactive engagement with external innovation and industry trends.

Project Management: Experience in leading small projects, coordinating activities, and managing timelines to meet project goals.

Supervisory Experience: preferred

Other Information

Initial location at Lilly Technology Center, Indianapolis.

Permanent location at the new Lilly Medicines Foundry in Lebanon, Indiana.

Limited domestic and international travel ( Role requires ability to work in manufacturing and laboratory environments.

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 (https://careers.lilly.com/us/en/workplace-accommodation) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.

Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status.

Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ+ Allies), Veterans Leadership Network (VLN), Women’s Initiative for Leading at Lilly (WILL), enAble (for people with disabilities). Learn more about all of our groups.

Actual compensation will depend on a candidate’s education, experience, skills, and geographic location. The anticipated wage for this position is

$129,000 - $209,000

Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly’s compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees.

#WeAreLilly

#J-18808-Ljbffr\n","Overview\nAt Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered ...","Advisor - Purification Process Translation and Execution Lilly Medicine Foundry",["B","2422888650"],"Work at Eli Lilly and Company","3 days ago","/jobs/2422888650-advisor-purification-process-translation-and-execution-lilly-medicine-foundry","Advisor - Purification Process Translation and Execution Lilly Me...","/jobs?keyword=Eli+Lilly+and+Company","/jobs?keyword=Advisor+-+Purification+Process+Translation+and+Execution+Lilly+Me...",{"_426":425,"_430":548,"_449":450,"_441":536,"_240":549,"_437":550,"_424":425,"_111":551,"_428":191,"_429":191,"_451":450,"_439":440,"_422":552,"_452":541,"_427":115,"_473":553,"_457":554,"_475":555,"_476":440,"_478":545,"_480":481,"_482":556},["D",1768946400000],"Advisor - Process Translation and Execution – Biologics & Hybrid - Lilly Medicine Foundry

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.\nOrganization And Function Overview\nLilly recently announced a $4.5 billion investment to create the Lilly Medicine Foundry, a pioneering center that integrates advanced manufacturing and drug development. As the first facility of its kind, the Foundry is designed to accelerate innovation in manufacturing processes, expand capacity for clinical trial medicines, and speed Lilly innovative medicine to Clinics, and reduce both costs and environmental impact.\nThe Process Translation and Execution (PTE) team plays a critical role in this mission. PTE is responsible for leading technology transfers from lab or pilot scale to cGMP production, collaborating with Operations and cross-functional teams to ensure reliable clinical supply and right-first-time production. The team also drives continuous improvement, advances the site technical agenda, and researches transformative technologies and champions the accelerated adoption of innovation in clinical and commercial manufacturing, ultimately delivering patient-centric outcomes.\nWe are seeking enthusiastic scientists and engineers to join the PTE team and help bring the Lilly Medicine Foundry’s vision to life.\nKey Responsibilities\nProcess Transfer and Scale-Up: Oversee the successful transfer of new biologics and or bioconjugates processes from development to manufacturing, ensuring scalability and process fit to plant.\nProcess Optimization and Improvement: Apply scientific knowledge to troubleshoot production issues, identify areas for improvement, and implement new technologies or procedures.\nData Analysis and Reporting: Monitor manufacturing processes, analyze experimental and production data, and author technical reports, protocols, and change controls.\nDocumentation and Compliance: Support the creation and review of technical documents, batch records, process descriptions, and risk assessments, ensuring adherence to cGMP and regulatory standards.\nCross-Functional Collaboration: Work closely with various departments across CMC, including Product Research and Development, Manufacturing, Quality, to achieve project goals and ensure product quality.\nInvestigations and CAPA Support: Lead or assist in process-related investigations, assess deviations, and support Corrective and Preventive Actions (CAPAs) to maintain product quality and timelines.\nTechnical Expertise and Training/Mentoring: Provide scientific input during audits, provide on-floor support for critical operations, and training/mentoring or supervising junior scientists or technicians in laboratory procedures, data analysis and all PTE activities.\nBasic Requirements\nEducation: BS, MS or PhD in Biology, Biochemistry, Biological Engineering, Chemical/Biochemical Engineering, or related disciplines\nExperience: BS with 15+ years, or MS with 10+ years, or PhD with 4+ years in Biologics/Drug Conjugates Product/Process Development, Manufacturing Technical Services, or related functional roles\nAdditional Skills And Preferences\nTechnical Expertise: Strong knowledge of bioprocesses (upstream or downstream), cell culture, bioreactor operation, centrifugation, filtration, chromatography, conjugation, and aseptic processing.\nProblem-Solving Skills: Proven ability to analyze data, perform root cause analysis, and resolve complex technical challenges.\nCommunication Skills: Excellent written and verbal communication skills for technical report writing, presentations, and effective collaboration across teams.\nCollaboration: Demonstrated success in cross-functional, dynamic, and matrixed environments.\nRegulatory Knowledge: Solid understanding of biopharmaceutical manufacturing principles and cGMP requirements.\nProject Management: Experience leading small projects, coordinating activities, and managing timelines to meet project goals.\nSupervisory Experience: highly preferred\nScientific Curiosity: Proactive engagement with external innovation and industry trends.\nOther Information\nInitial location at Lilly Technology Center, Indianapolis.\nPermanent location at the new Lilly Medicines Foundry in Lebanon, Indiana.\nLimited domestic and international travel ( Role requires ability to work in manufacturing and laboratory environments.\nLilly 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 for further assistance. Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status.\nOur employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Learn more about all of our groups.\nActual compensation will depend on a candidate’s education, experience, skills, and geographic location. The anticipated wage for this position is $121,500 - $198,000. Full-time employees are eligible for a company bonus and a comprehensive benefits program.\n#WeAreLilly

#J-18808-Ljbffr\n","Advisor - Process Translation and Execution – Biologics & Hybrid - Lilly Medicine Foundry

At Lilly, we unite caring with discovery to make...","Advisor - Process Translation and Execution – Biologics & Hybrid - Lilly Medicin",["B","2213229890"],"17 days ago","/jobs/2213229890-advisor-process-translation-and-execution-biologics-hybrid-lilly-medicin","Advisor - Process Translation and Execution – Biologics & Hybrid ...","/jobs?keyword=Advisor+-+Process+Translation+and+Execution+%E2%80%93+Biologics+%26+Hybrid+...","actionData","errors"]