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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.

In the Project Delivery Phase and Startup Phase of the project (2025 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.

The Laboratory Informatics Scientist role, a technical-track position with an emphasis on electronic laboratory notebook (ELN) development and template design, seeks a collaborative, inclusive, and energetic individual who will play a key role in building and supporting the digital ecosystem that powers the Lilly Medicine Foundry laboratories, with a primary focus on designing and deploying structured ELN templates across multiple platforms including LabVantage ELN, Signals, and Benchling. The role will help implement, configure, and maintain critical laboratory informatics platforms, including ELN/LES, LIMS, MODA, Empower, and other systems that enable efficient, compliant scientific operations. This position is ideal for someone with experience in ELN template development, non-GMP development workflows, or technology transfer who thrives at the intersection of science, technology, and quality. You will collaborate with global and local IT teams, laboratory scientists, process chemists, biologists, and quality partners to ensure data integrity, system reliability, and seamless lab workflows. As the systems mature, your role will evolve into serving as the site ELN subject matter expert across all modalities, leading continuous improvement initiatives for notebook workflows, mentoring users, supporting audits, and executing long-term digital strategy for the lab. This is a unique opportunity to grow your informatics career within a state-of-the-art digital laboratory environment and help shape foundational capabilities for the Medicine Foundry.

**Responsibilities**

- Configure, deploy, and support laboratory informatics platforms, with primary ownership of ELN systems (LabVantage ELN, Signals, Benchling), and cross-trained backup support for LIMS, MODA, LES, and Empower.

- Design, develop, and maintain structured ELN templates, notebook forms, and review/approval workflows that work harmoniously across multiple ELN platforms.

- Participate in system installation, qualification, validation activities, and periodic reviews to maintain a validated state.

- Troubleshoot system issues and serve as a primary technical point of contact (SME) for lab users.

- Monitor the performance of laboratory informatics systems to ensure data integrity, compliance, and efficiency.

- Drive enhancements to ELN templates, digital workflows, automation opportunities, and end‑user experience.

- Support continuous improvement initiatives aligned with quality systems and laboratory operations.

- Maintain compliance with cGMP/GLP and data integrity expectations across laboratory systems.

- Prepare and author quality system deliverables, including management review summaries, deviations, CAPAs, and system documentation.

- Support internal and external audit readiness and represent laboratory systems during inspections.

- Develop training materials and deliver user training for new systems, functionality, or processes.

- Partner closely with scientists and IT teams to align system functionality with lab needs.

- Contribute to project planning, timelines, and resource recommendations for lab informatics initiatives.

- Model an inclusive, collaborative mindset that encourages diverse perspectives and creative problem‑solving.

**Basic Requirements**

- B.S. in Computer Science, Information Systems, Chemistry, Biology, Engineering, or related discipline, with 3+ years experience OR H.S./Associates degree with 5+ years experience supporting or administering laboratory informatics systems (ELN, LIMS, LES, QC systems, or similar), with preference for hands-on ELN template development or configuration experience in a regulated environment (GxP, GLP, GMP).

- Hands‑on experience with computerized system validation (CSV) concepts and data integrity requirements.

- Experience configuring systems, populating master data, or supporting system deployment/upgrade activities.

- Qualified candidates must be legally authorized to be employed in the United States. Lilly does not anticipate providing sponsorship for employment visa status (e.g., H-1B or TN status) for this employment position

**Additional Preferences**

- Familiarity with end‑to‑end analytical workflows in a QC or development lab

- Proficiency with computer systems including Microsoft Office products, LIMS, Laboratory Execution Systems, chromatography systems, electronic laboratory notebook systems (e.g., Signals, Benchling, LabVantage ELN) including template development and implementation of systems.

- Demonstrated ability to drive and accept change.

- Good interpersonal skills and a sustained tendency for collaboration.

- Demonstrated success in persuasion, influence, and negotiation.

- Ability to prioritize multiple activities and manage ambiguity.

- Must possess strong communication (oral, written), organizational, and leadership 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

$65,250 - $169,400

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

Lab Informatics Scientist – ELN Design/Development - 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.

**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.

In the Project Delivery Phase and Startup Phase of the project (2025 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.

The Laboratory Informatics Scientist role, a technical-track position with an emphasis on environmental monitoring and MODA platform support, seeks a collaborative, inclusive, and energetic individual who will play a key role in building and supporting the digital ecosystem that powers the Lilly Medicine Foundry laboratories, with a primary focus on deploying and sustaining the MODA environmental monitoring platform. The role will help implement, configure, and maintain critical laboratory informatics platforms, including MODA, LIMS, ELN/LES, Empower, and other systems that enable efficient, compliant scientific operations. This position is ideal for someone with experience in environmental monitoring workflows, EM sampling plans, and microbiological data management who thrives at the intersection of science, technology, and quality. You will collaborate with global and local IT teams, laboratory scientists, microbiology teams, and quality partners to ensure data integrity, system reliability, and seamless lab workflows. As the systems mature, your role will evolve into serving as the site MODA subject matter expert, leading continuous improvement initiatives for EM processes, mentoring users, supporting audits, and executing long-term digital strategy for the lab. This is a unique opportunity to grow your informatics career within a state-of-the-art digital laboratory environment and help shape foundational capabilities for the Medicine Foundry.

**Responsibilities**

- Configure, deploy, and support laboratory informatics platforms, with primary ownership of the MODA environmental monitoring system, and cross-trained backup support for LIMS, ELN, LES, and Empower.

- Configure and maintain EM sampling plans, location hierarchies, alert/action limits, organism panels, and master data across laboratory informatics systems.

- Participate in system installation, qualification, validation activities, and periodic reviews to maintain a validated state.

- Troubleshoot system issues and serve as a primary technical point of contact (SME) for lab users.

- Monitor the performance of laboratory informatics systems, including EM trending, excursion management, and deviation support within MODA, to ensure data integrity, compliance, and efficiency.

- Drive enhancements to digital workflows, automation opportunities, and end‑user experience.

- Support continuous improvement initiatives aligned with quality systems and laboratory operations.

- Maintain compliance with cGMP/GLP and data integrity expectations across laboratory systems.

- Prepare and author quality system deliverables, including management review summaries, deviations, CAPAs, and system documentation.

- Support internal and external audit readiness and represent laboratory systems during inspections.

- Develop training materials and deliver user training for new systems, functionality, or processes.

- Partner closely with scientists and IT teams to align system functionality with lab needs.

- Contribute to project planning, timelines, and resource recommendations for lab informatics initiatives.

- Model an inclusive, collaborative mindset that encourages diverse perspectives and creative problem‑solving.

**Basic Requirements**

- B.S. in Computer Science, Information Systems, Chemistry, Biology, Engineering, or related discipline, with 3+ years experience OR H.S./Associates degree with 5+ years experience supporting or administering laboratory informatics systems (LIMS, ELN, LES, MODA, environmental monitoring systems, QC systems, or similar) in a regulated environment (GxP, GLP, GMP).

- Hands‑on experience with computerized system validation (CSV) concepts and data integrity requirements.

- Experience configuring systems, populating master data, or supporting system deployment/upgrade activities.

- Qualified candidates must be legally authorized to be employed in the United States. Lilly does not anticipate providing sponsorship for employment visa status (e.g., H-1B or TN status) for this employment position

**Additional Preferences**

- Familiarity with end‑to‑end analytical workflows in a QC or development lab

- Proficiency with computer systems including Microsoft Office products, LIMS, Laboratory Execution Systems, chromatography systems, electronic laboratory notebook systems including implementation of systems.

- Demonstrated ability to drive and accept change.

- Good interpersonal skills and a sustained tendency for collaboration.

- Demonstrated success in persuasion, influence, and negotiation.

- Ability to prioritize multiple activities and manage ambiguity.

- Must possess strong communication (oral, written), organizational, and leadership 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

$65,250 - $169,400

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

Laboratory Informatics Scientist - Lilly Medicine Foundry

We're a medicine company turning science into healing to make life better for people around the world. It all started nearly 150 years ago with a clear vision from founder Colonel Eli Lilly: "Take what you find here and make it better and better." Harnessing the power of biotechnology, chemistry and genetic medicine, our scientists are urgently advancing science to solve some of the world's most significant health challenges.

General Information and Guidelines:
When you engage with us on LinkedIn, you're agreeing to these Community Guidelines: https://e.lilly/guidelines. 

If you have questions about a Lilly medicine, contact The Lilly Answers Center at 1-800-Lilly-Rx (1-800-545-5979) Monday through Friday, excluding company holidays.

Industry: Pharmaceutical Manufacturing
Company Size: 10,001+ employees

Eli Lilly and Company

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 opened a cutting edge manufacturing facility dedicated to genetic medicines at Lebanon, Indiana. This facility is Lilly’s most technically advanced manufacturing site focused on the delivery of the next wave of innovative products. It includes next-generation manufacturing technologies and advanced data collection and analysis platforms that will deliver improvements in safety and quality, and process performance. This is a unique opportunity to be a part of the team for the startup of a greenfield manufacturing site, and the successful candidate will help to design, commission and start up the facility for both clinical and commercial supply.

This is an exciting opportunity to help build a state-of-the-art facility and Quality System from the ground up. The TS/MS team will own all areas of technology transfer, process validation, and process stewardship.

**Position Description**

Drug Product Bioprocess Scientist – Technical Services/Manufacturing Scientist (TS/MS) role is responsible for providing technical support for the development, implementation, and execution of compliant manufacturing of gene therapy drug product. The scope of the role will initially focus on formulation, media & buffer preparation, Drug Product Filling & packaging and visual inspection operations, from facility startup through support of validation processes and commercial manufacturing.

**Key Objectives/Deliverables**

- Provide technical support for internal and external TS/MS activities (e.g., tech transfer, process validation, investigation, media & buffer recipe, formulation, filling & packaging and visual inspection)

- Understand the scientific principles required for manufacturing gene therapy drug products, including the interaction of the chemistry, equipment, aseptic processes, and container closure systems

- Responsible for ensuring that formulation issues are addressed and resolved

- Ownership and technical stewardship of media and buffer preparation formulations

- Prepare, review, approve, and provide technical support for preparation of relevant technical documents, as required, such as: change controls, regulatory submissions, deviation investigations, validation protocols and summary reports, processing records, process description documents and annual reports.

- Support and/or lead TS/MS technical projects to ensure a successful start-up, improve process control, yield, product quality and/or productivity. Implement process changes and improvements through the technical agenda.

- Develop, monitor, and appropriately react to established statistically based metrics in real-time to assess process variability and capability

- Apply manufacturing process knowledge and data analysis skills to support the management of daily manufacturing operations

- Serve as technical interface external to the Lebanon site.

- Provide audit support, as needed.

- Work within or lead cross-functional teams in a positive fashion to implement TS/MS objectives and deliver on business plan and quality objectives.

- Ensure a safe working environment through compliance with safety rules and improve safety culture by actively participating in safety-related activities

**Basic Requirements**

- BS in Chemical Engineering, Biochemical Engineering, Chemistry, Biochemistry or related quantitative field

- 3+ years of experience in cGMP manufacturing, specifically within Operations, Validation, TS/MS, Engineering, or Quality Assurance.

- 3+ years experience with parenteral drug product manufacturing, particularly with formulation, technical transfer, visual inspection, statistical data trending and analysis and process risk assessment (e.g. FMEA).

**Additional Preferences**

- In depth knowledge of gene therapy drug product manufacturing

- Experience with AAV drug product formulation, media and buffer preparation will be a plus

- Experience using solution filling equipment and/or isolator technology

- Experience with serialization and packaging

- Strong interpersonal and teamwork skills

- Strong self-management and organizational skills

- Strong oral and written communication skills that demonstrate an ability to effectively (clearly, succinctly) communicate with all levels of the organization

- Experience with data trending and analysis

- Ability to analyze complex data and solve problems

- Demonstrated successful membership/leadership of cross-functional teams

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

$66,000 - $171,600

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

Bioprocess Scientist (Drug Product) - Advanced Therapies Manufacturing

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 opened a cutting edge manufacturing facility dedicated to genetic medicines at Lebanon, Indiana. This facility is Lilly’s most technically advanced manufacturing site focused on the delivery of the next wave of innovative products. It includes next-generation manufacturing technologies and advanced data collection and analysis platforms that will deliver improvements in safety and quality, and process performance. This is a unique opportunity to be a part of the team for the startup of a greenfield manufacturing site, and the successful candidate will help to design, commission and start up the facility for both clinical and commercial supply.

This is an exciting opportunity to help build a state-of-the-art facility and Quality System from the ground up. The TS/MS team will own all areas of technology transfer, process validation, and process stewardship.

**Position Description**

Downstream Bioprocess – Technical Services/Manufacturing Scientist (TS/MS) role is responsible for providing technical support for the development, implementation, and technical transfer of compliant manufacturing of gene therapy drug substance for clinical and commercial manufacture. The successful candidate will be required to build deep technical expertise in their area of responsibility (including in-depth knowledge of the science behind the molecule and the process), have strong working skills on the manufacturing equipment set and control systems, and consistently demonstrate strong data-driven decision-making and problem-solving capabilities. They may also work to ensure that the process is in-control, capable, compliant, and maintained in a validated state through continual monitoring and may play a role in by implementing new technologies and process improvements in the manufacturing environment.

**Key Objectives/Deliverables**

- Have an in-depth knowledge of the science behind the molecule and the processes. Understand the process control strategy for AAV and gene therapy products

- Provide technical support for internal and external TS/MS activities (e.g., tech transfer, process validation, investigation, process stewardship and improvement)

- Understand the scientific principles required for manufacturing AAV drug substances and products, and have extensive hands-on experience on chromatography operation, TFF, viral filtration and sterile filtration

- Ownership and technical stewardship of bioprocess and provide technical expertise during Root Cause Analysis for deviations and Impact Assessments for changes

- Work as part of cross-functional teams, and establish partnerships with applicable functions, operations, and development to understand interface between the science/engineering with the operations on the floor and bring deep technical expertise to the team

- Be able to assess whether the process is in control and capable of meeting its stated purpose and is in a constant state of validation

- Identify process improvements and participate in implementation of Lean manufacturing initiatives

- Prepare, review, approve, and provide technical support for preparation of relevant technical documents, as required, such as: change controls, regulatory submissions, deviation investigations, validation protocols and summary reports, processing records, process description documents and annual reports

- Support and/or lead TS/MS technical projects to ensure a successful start-up, improve process control, yield, product quality and/or productivity. Implement process changes and improvements through the technical agenda

- Develop, monitor, and appropriately react to established statistically based metrics in real-time to assess process variability and capability

- Serve as technical interface external to the Lebanon site

- Provide audit support, as needed

- Work within or lead cross-functional teams in a positive fashion to implement TS/MS objectives and deliver on business plan and quality objectives.

- Ensure a safe working environment through compliance with safety rules and improve safety culture by actively participating in safety-related activities

**Basic Requirements**

- B.S. in Biochemical Engineering, Chemical Engineering, Biotechnology, Biochemistry or related quantitative field

- 3+ years of experience in cGMP manufacturing, specifically within Operations, Validation, TS/MS, or Engineering

**Additional Preferences**

- In depth knowledge of gene therapy manufacturing

- Experience with large scale AAV vector production using single use bioreactor systems

- Experience using solution filling equipment and/or isolator technology

- Experience with QC assays in line with product CQAs including variability

- Strong interpersonal and teamwork skills

- Strong self-management and organizational skills

- Strong oral and written communication skills that demonstrate an ability to effectively (clearly, succinctly) communicate with all levels of the organization

- Experience with data trending and analysis

- Ability to analyze complex data and solve problems

- Demonstrated successful membership/leadership of cross-functional teams

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

$66,000 - $171,600

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

Bioprocess Scientist (Downstream) - Advanced Therapies Manufacturing

Tata Consultancy Services is an IT services, consulting and business solutions organization that has been partnering with many of the world’s largest businesses in their transformation journeys for over 55 years. Its consulting-led, cognitive powered, portfolio of business, technology and engineering services and solutions is delivered through its unique Location Independent Agile™ delivery model, recognized as a benchmark of excellence in software development.  

A part of the Tata group, India's largest multinational business group, TCS has over 603,305 of the world’s best-trained consultants in 55 countries. The company generated consolidated revenues of US $27.9 billion in the fiscal year ended March 31, 2023, and is listed on the BSE and the NSE in India. TCS' proactive stance on climate change and award-winning work with communities across the world have earned it a place in leading sustainability indices such as the MSCI Global Sustainability Index and the FTSE4Good Emerging Index. For more information, visit www.tcs.com   

*Caution against fraudulent job offers*: TCS doesn't charge any fee throughout the recruitment process. Refer here: on.tcs.com/3i9X5BU

Industry: IT Services and IT Consulting
Company Size: 10,001+ employees

Tata Consultancy Services

**Job Description**

DMust Have Technical/Functional Skills

Desktop support, L2 Windows support, Mac OS support, Windows 10/11, Apple iOS Support,

Roles & Responsibilities

-  Provide remote desktop level L2 troubleshooting of end user issues by taking remote control of

Laptop/Desktop/VDI

-  Solving technical issues related to Windows 10/11, iOS and Mac operating systems and standard software components

like MS Office/VPN/Anti-Virus/Skype etc.

-  Provide support in enrolling the iOS devices in MDM (JAMF) and investigate the incidents and Tasks

-  Deployment of device drivers and windows patch updates

-  Troubleshoot laptop/desktop performance, group policy, Encryption and failed Software configuration of end user devices

-  Manage the Security compliance health status of end user workstations

-  Working knowledge of enterprise Ticketing tool like ServiceNow

-  Diagnoses, troubleshoot, resolve and escalate supported software, hardware and peripheral Incident calls assigned from

Service Desk team

-  Adjust configuration options as required to resolve defects identified while performing corrective action on a device

-  Investigate desktop level incidents and identify root causes to be able to provide solutions.

-  Deployment, Monitoring, Reporting of Device Drivers including BIOS & utilities

-  Support Windows 11 Feature upgrade using modern management techniques - Intune/Auto Pilot

-  L2 Workstations operational support

-  Monitor and report on User experience.

-  Report on Workstation image deployments and patch compliance metrics

Salary Range $60,000-$65,000 years

**TCS Employee Benefits Summary**

Discretionary Annual Incentive.

Comprehensive Medical Coverage: Medical & Health, Dental & Vision, Disability Planning & Insurance, Pet Insurance Plans.

Family Support: Maternal & Parental Leaves.

Insurance Options: Auto & Home Insurance, Identity Theft Protection.

Convenience & Professional Growth: Commuter Benefits & Certification & amp; Training Reimbursement.

Time Off: Vacation, Time Off, Sick Leave & Holidays.

Legal & Financial Assistance: Legal Assistance, 401K Plan, Performance Bonus, College Fund, Student Loan Refinancing.

**Qualifications: **BACHELOR OF COMPUTER SCIENCE

Desktop And Mobility Support

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