Indianapolis, Indiana, United States · On-site
$65k–$169k/yr
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. Headqua…
Skills: GMP Microbiology, Sterility Testing, Bioburden Testing, Bacterial Endotoxin Test, Microbial Limits Testing
Indianapolis, Indiana, United States · On-site
$152k–$240k/yr
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Skills: Parenteral Drug Product Development, Process Engineering, Fill/Finish, Compounding, Scale-up
Indianapolis, Indiana, United States · Hybrid
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Overview This position is responsible for the Fleet Warranty Customers in assigned territory. The Warranty Coordinator should be highly organized, exhibit technical proficiency and the ability to communicate well with ma…
Skills: Warranty Processing, Technical Proficiency, Customer Service, Vendor Management, Fleet Management
Indianapolis, Indiana, United States · On-site
$16/hr–$21/hr
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Skills: Assembly, Quality Control, Hand Tool Operation, Power Tool Operation, Technical Drawing Interpretation
Indianapolis, Indiana, United States · Remote OK
$150k–$180k/yr
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Indianapolis, Indiana, United States · On-site
$44k–$85k/yr
We’re building a world of health around every individual — shaping a more connected, convenient and compassionate health experience. At CVS Health®, you’ll be surrounded by passionate colleagues who care deeply, innovate…
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Indianapolis, Indiana, United States · On-site
$99k–$160k/yr
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Indianapolis, Indiana, United States · On-site
Shift: 6:30 AM-4:00 PM Hourly Rate: $19.12 an hour ESSENTIAL JOB FUNCTIONS: You demonstrated behaviors to support company safety procedures with focus on zero injuries. You support quality work processes You follow and c…
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Indianapolis, Indiana, United States · Hybrid
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Indianapolis, Indiana, United States · Remote OK
$101k–$161k/yr
At ABB, we help industries run leaner and cleaner—and every person here makes that happen. You’ll be empowered to lead, supported to grow, and proud of the impact we create together. Join us and help run what runs the wo…
Skills: Channel Sales Strategy, Distributor Planning, Sales Productivity, Channel Partner Relationship Management, Coaching
Indianapolis, Indiana, United States · On-site
$65k–$169k/yr
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. Headqua…
Skills: Environmental Monitoring, GMP Compliance, Aseptic Manufacturing, Root Cause Investigation, Contamination Control Strategy
Indianapolis, Indiana, United States · On-site
$152k–$264k/yr
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Skills: LNP Process Development, TNP Process Development, Fill/Finish, Scale-up, CMC Development
Indianapolis, Indiana, United States · On-site
Our team members are at the heart of everything we do. At Cencora, we are united in our responsibility to create healthier futures, and every person here is essential to us being able to deliver on that purpose. If you w…
Skills: Order Fulfillment, Cycle Counting, Picking and Packing, Outbound Shipping, RF Scanning
Indianapolis, Indiana, United States · Hybrid
$79k–$128k/yr
Job Description Job Title: Development Engineer Working Pattern: Hybrid/Onsite in office 3 days/week Working location: Indianapolis, IN Relocation is available for this position if appropriate Job Expires: August 5, 2026…
Skills: Technical Project Management, Development Engineering, Certification Planning, Verification Testing, Risk Management
Indianapolis, Indiana, United States · On-site
$66k–$172k/yr
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. Headqua…
Skills: Packaging Engineering, Vendor Management, Project Management, Root Cause Analysis, Sustainability
Indianapolis, Indiana, United States · On-site
$30/hr–$35/hr
Position Summary Trailer Technician/Mechanic – Indianapolis, IN $30.00 - $35.00 hr | Weekly Pay | Full Benefits within 30 Days Amerit Fleet Solutions, a leader in fleet maintenance across the U.S., is hiring a skilled Tr…
Skills: Trailer Maintenance, Mechanical Troubleshooting, Electrical Diagnostics, Preventive Maintenance, Safety Compliance
Indianapolis, Indiana, United States · On-site
Shift: 6:30 AM-4:00 PM Hourly Rate: $19.12 an hour ESSENTIAL JOB FUNCTIONS: You demonstrated behaviors to support company safety procedures with focus on zero injuries. You support quality work processes You follow and c…
Skills: Equipment Operation, Sanitization, Quality Control, Safety Compliance, GMP
Fayetteville, Arkansas, United States · On-site
$59k–$79k/yr
This job posting is an “Evergreen Requisition” designed to gather talent for current or future open positions. It Is a way for Conagra to expedite the hiring process when there is a need to fill that type of role. By app…
Skills: Supply Chain Management, Logistics, Data Analysis, Project Management, Problem Solving
Indianapolis, Indiana, United States · On-site
Job Description Job Title: Machine Repair/Equipment Builder Working Pattern: Onsite 9/80 Working location: Indianapolis, IN As a Machine Repair/Equipment Builder, you will develop and build a variety of special machines,…
Skills: Machine Construction, CNC Equipment Repair, Machine Tool Operation, Blueprint Reading, Shop Math
Indianapolis, Indiana, United States · Hybrid
$79k–$128k/yr
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Indianapolis, Indiana, United States • On-site
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The role serves as a subject matter expert overseeing microbiological testing and batch disposition for clinical GMP manufacturing. Key duties include leading laboratory investigations, authoring SOPs, and mentoring junior analysts to ensure regulatory compliance.
Requires a BS or MS in Microbiology or a related science with 3-5+ years of cGMP pharmaceutical microbiology experience. Candidates should be proficient in compendial method execution and experienced in authoring investigations and mentoring staff.
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.
Lilly recently announced a $4.5 billion investment to create the Lilly Medicine Foundry — the first-ever facility to combine research and manufacturing in a single location, expanding capacity for clinical trial medicines while reducing costs and environmental impact.
Analytical GMP Laboratories (AGL) supports GMP testing across the Lilly Medicine Foundry (LMF) and the broader Product Research & Development (PRD) network, spanning environmental monitoring, microbiology, GMP testing, raw materials, and cleaning/investigations. AGL sits at the intersection of science and quality — this role offers the opportunity to shape the analytical compliance program from the ground up and help drive quality culture at a cutting-edge facility.
The Principal Scientist, GMP QC Microbiology is the subject matter expert supporting the Sr. Advisor of Env. Monitoring & Microbiology in day-to-day microbiological testing and batch disposition for clinical GMP manufacturing at the Medicine Foundry Analytical GMP Laboratory. The role executes and oversees compendial and non-compendial microbiological testing including sterility, bioburden, endotoxin (Bacterial Endotoxin Test), microbial limits, and water testing; leads laboratory investigations; authors change controls and SOPs; and trains and mentors junior analysts. Partnering with the Sr. Advisor, Quality Assurance, Manufacturing, and Regulatory Affairs, the role contributes to method validation and inspection readiness in compliance with cGMP, data integrity (ALCOA+), EU GMP Annex 1, and applicable global regulatory requirements.
What You'll Do
Testing & batch disposition
Perform and oversee sterility, bioburden, microbial limits, and water system testing; serve as primary data reviewer for accurate and timely batch disposition.
Perform microbial identification testing and maintain the site isolate library; support EM activities as back-up coverage.
Method validation & change control
Lead method validations, transfers, and verifications; prepare protocols and summary reports and author change controls for test methods, specifications, and SOPs.
Support qualification of laboratory equipment and evaluate new rapid microbiological methods (RMM).
Investigations, OOS & CAPA
Lead OOS/OOT and other laboratory investigations; author deviation reports and drive CAPA to closure with QA.
Regulatory compliance & audit readiness
Maintain documentation in a state of inspection readiness, serve as SME during inspections and audits, and support remediation of audit observations to closure.
Stay current on applicable compendial standards and regulatory requirements; update SOPs to reflect evolving requirements.
Training, mentorship & continuous improvement
Develop and deliver training for junior analysts on test methods, aseptic technique, and cGMP; serve as a qualified trainer; and maintain training records and competency matrices.
Partner with the Advisor on lab workflow and continuous improvement initiatives. Handle biohazardous and hazardous materials per EHS requirements.
Safety and GMP execution
Ensure laboratory, cleanroom, and manufacturing support activities are performed safely and in accordance with approved procedures, cleanroom behaviors, and GMP expectations.
Minimum Qualifications
BS or MS in in Microbiology, Biology, Biochemistry, Pharmaceutical Sciences, or related technical discipline
BS with 5+ years or MS with 3+ years of experience in cGMP pharmaceutical microbiology experience, including compendial method execution, investigation authoring, and analyst mentoring.
Equivalent combinations of education and cGMP microbiology experience will be considered.
Additional Skills and Preferences
Experience with aseptic manufacturing or sterile drug product operations (fill–finish, lyophilization).
Proficiency with EM data systems including MODA, LabVantage, Metasys, and quality management systems (TrackWise, Veeva Vault).
Experience with RMM platforms (BacT/ALERT, Bactec, Milliflex, NAT/PCR sterility). Prior work with LIMS, ELN, LabVantage, TrackWise, or Veeva Vault.
Working knowledge of microbial identification techniques (MALDI-TOF, Vitek, Gram stain).
Experience working in a greenfield or start-up laboratory environment, including contributing to lab build-out, SOP authoring from scratch, equipment selection and qualification, and establishing a quality culture from the ground up.
Additional Information
Location: Initial location at Parkwood West, Carmel, IN, with occasional work at Lilly Technology Center, Indianapolis. Permanent location at the Lilly Medicine Foundry in Lebanon, IN.
Travel: Less than 5% domestic
Regular work in controlled cleanroom environments (ISO 5–8 / Grade A–D) requiring gowning per applicable SOP requirements.
May require occasional off-hours, weekend, or on-call availability to support critical manufacturing campaigns or investigation response.
Physical requirements include standing for extended periods, walking throughout the facility, and performing gowning activities.
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 (AMECA), Black Employees at Lilly (BE@Lilly), Chinese Culture Network (CCN), EnAble, Evolve, Lilly Indian Network (LIN), Organization of Latinx at Lilly (OLA), Pride (LGBTQ+ Allies), Veterans Leadership Network (VLN) and Women’s Initiative for Leading at Lilly (WILL).
Actual compensation will depend on a candidate’s education, experience, skills, and geographic location. The anticipated wage for this position is
$65,250 - $169,400Full-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
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.
Offices: Lilly Corporate Center, Indianapolis, Indiana 46285, US
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