Jazz PharmaceuticalsNewMedical Science Liaison, Neuro-Oncology - Central Jazz PharmaceuticalsMedical Science Liaison, Neuro-Oncology - CentralIndianapolis, INRemote$160,000–$240,000 / yearThe successful candidate may also be eligible for a discretionary annual cash bonus or incentive compensation (depending on the role), in accordance with the terms of the Company's Global Cash Bonus Plan or Incentive Compensation Plan, as well as discretionary equity grants in accordance with Jazz's Long Term Equity Incentive Plan. This is a field-based position covering Kansas, Missouri, Illinois, Kentucky, Ohio, Indiana, Iowa, Michigan, Wisconsin, Minnesota, North Dakota, and South Dakota, and requires professionals with established personal and scientific credibility to interact with thought leaders and academic centers of excellence.
Fast Pace HealthNewPRN Family Nurse Practitioner Fast Pace HealthPRN Family Nurse PractitionerAnderson, INThey must have the ability to respond quickly and accurately to changes in condition or response to treatment and is responsible for providing outstanding patient service within the clinic and through various virtual communication channels, while maintaining a compassionate and welcome atmosphere. Posting Title: PRN Family Nurse Practitioner Overview: In a manner consistent and supportive of our values, the Provider is responsible for delivering high quality health care within Fast Pace Health’s scope of services while achieving optimum patient satisfaction.
Katalyst Healthcares and Life SciencesNewRegulatory Affairs Coordinator Katalyst Healthcares and Life SciencesRegulatory Affairs CoordinatorIndianapolis, INThey will support clinical research teams by facilitating the study start-up approval process and maintaining documentation of regulatory compliance throughout the trial's duration for research studies involving human subjects . This role ensures adherence to local, state, and federal regulations, including but not limited to FDA, ICH, and GCP guidelines, and supports the smooth conduct of clinical research studies at the site.
ElancoRegulatory Affairs Consultant- R&D ElancoRegulatory Affairs Consultant- R&DGreenfield, INFull timeAdditionally, demonstrate leadership by providing innovative solutions, promoting a positive work environment, and effectively communicating to ensure delivery and maintenance of Elanco’s food animal and pet health pharmaceutical portfolio. Elanco reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion, and Elanco’s compensation practices and guidelines will apply regarding the details of any promotion or transfer of Elanco employees.
ElancoSenior Regulatory Affairs Scientist – Animal Health Biologics (CMC, USDA) ElancoSenior Regulatory Affairs Scientist – Animal Health Biologics (CMC, USDA)Greenfield, INFull timeIn this role, you will partner closely with Manufacturing, Quality, R&D, and regulatory authorities to deliver innovative regulatory solutions that support the Elanco pipeline and sustain established biological products. As the Senior Regulatory Affairs Scientist, you will provide strategic regulatory guidance to ensure comprehensive, cohesive, and compliant submissions that maintain global product registrations and availability.
AES CorporationNewManager, Regulatory Affairs AES CorporationManager, Regulatory AffairsUS, Indianapolis, INUnder limited supervision, the Manager, Regulatory Affairs is responsible for leading a small team responsible for designing tariffs and prepare testimony to the Indiana Utility Regulatory Commission coordinating filings with and testifying before the Indiana Regulatory Commission providing financial, technical, and regulatory analysis supporting senior management assimilating technical and economic information into rate design, and reviewing and providing comment on proposed State and Federal legislation and proposed rules and regulations. AES is proudly ranked #1 globally in renewable energy sales to corporations, and with $12.7B in revenues in 2023, we have the resources and expertise to make a significant impact as we provide electricity to 25 million customers worldwide.
GovernmentJobs.comNewManager - Legislative Affairs & Policy GovernmentJobs.comManager - Legislative Affairs & PolicyIndianapolis, INThis position carries out broad and complex assignments requiring comprehensive knowledge—or the ability to obtain such knowledge—of public policy, legislative processes, and intergovernmental affairs in order to interpret and apply policies and provide information that supports decision-making. The Manager - Legislative Affairs & Policy analyzes, consolidates, and interprets data; prepares policy and fiscal reports; assists in the city-county budget process; and maintains a comprehensive understanding of state and federal policy trends affecting local governance.
The Heritage GroupGovernment Affairs Director The Heritage GroupGovernment Affairs DirectorIndianapolis, IndianaThe Government Affairs Director will support and advance the company's federal public policy objectives by managing its Federal Political Action Committee (PAC), identifying and pursuing federal opportunities-including grants, programs, and legislative initiatives-and building strong relationships with policymakers and industry partners. This role is ideal for a proactive, detail-oriented government affairs professional who is comfortable working across a diverse portfolio of companies and stakeholders and is comfortable being held accountable to results.
Canon USA & AffiliatesLeader Medical Affairs Canon USA & AffiliatesLeader Medical AffairsIndianapolis, INRemote10 years’ experience as a Medical Physicist, Scientist, or MD in a clinical hospital or clinical research setting or 3 years of experience as a Medical Physicist, Scientist, or MD in a clinical hospital or clinical research setting plus 7 years of experience in healthcare industry as imaging scientist or research manager. Analyze and communicate technical and clinical product specification requirements from luminaries, market research teams, and via Medical Advisory Boards (MABs) to global business team.
Langham LogisticsDocument Control and Regulatory Specialist Langham LogisticsDocument Control and Regulatory SpecialistIndianapolis, INThis position supports compliance across pharmaceutical logistics operations, including temperature-sensitive biologics, raw materials, vaccines and general pharmaceutical products, helping maintain audit readiness and alignment with cGMP, GDP, FDA, ICH and client requirements. The Document Control and Regulatory Specialist contributes to Langham Logistics' goals of exceptional customer service, quality, process improvement, and profitability by managing the document control system and supporting regulatory compliance activities across the organization.
Eli Lilly and CoSr. Director - Global Regulatory Lead - Neuroscience/Immunology Eli Lilly and CoSr. Director - Global Regulatory Lead - Neuroscience/ImmunologyIndianapolis, IN$169,500–$248,600 / yearOur 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). Primary Responsibilities: Regulatory and Scientific Expertise • Develop, Update and Implement the Global Regulatory Strategy - Initiate and Update Regulatory Strategy Document (RSD) • Obtain input from the global regulatory team members to develop a global regulatory strategy which supports product (including delivery device and relevant medical devices) development, registration, and lifecycle maintenance globally.
Wurth Industry USARegulatory Sustainability Analyst Wurth Industry USARegulatory Sustainability AnalystGreenwood, INThis role combines regulatory interpretation with operational data management to ensure the company can accurately assess, document, and report on regulatory obligations related to topics such as PFAS chemical disclosures, carbon reporting, environmental product disclosures and supply chain environmental transparency. The role works cross-functionally with supply chain, procurement, compliance, and sustainability teams to translate complex regulatory requirements into structured data collection processes and defensible reporting.
Stride, Inc.Compliance Coordinator Stride, Inc.Compliance CoordinatorIndianapolis, IndianaPrimary responsibilities include but are not limited to the submission of new and renewal applications, student performance data to various oversight agencies, maintaining point of contact information for oversight agencies, processing employment verifications, and distribution of internal compliance updates. The company partners with workforce organizations, healthcare providers, and academic institutions to help build talent pipelines and provide pathways to career advancement, including opportunities for articulated college credit.
AES CorporationNewNERC Operations Team Leader AES CorporationNERC Operations Team LeaderUS, Indianapolis, IN$108,500–$135,575 / yearThis position offers the opportunity to support AES’s rapidly growing renewable portfolio – including utility-scale solar, wind, battery storage, and other clean energy projects – and to play a pivotal role in maintaining the reliability and security of the Bulk Electric System while upholding industry-leading best practices. Regulatory Compliance Execution: Partner with Operations, Maintenance, Engineering, Protection and Control, Asset Management and NERC Compliance Teams to translate NERC regulatory requirements into executable processes, technical controls, maintenance programs and audit ready evidence.
Otsuka America PharmaceuticalNewAssociate Director, Global Quality Operations Otsuka America PharmaceuticalAssociate Director, Global Quality OperationsIndianapolis, INMinimum $150,034.00 - Maximum $224,250.00, plus incentive opportunity: The range shown represents a typical pay range or starting pay for individuals who are hired in the role to perform in the United States. The Associate Director, Quality Operations will lead initiatives that drive operational excellence, enhance risk management practices, and optimize global quality system processes across a global quality organization.
Elanco Animal Health IncSenior Research Scientist - Clinical Operations Elanco Animal Health IncSenior Research Scientist - Clinical OperationsIndianapolis, INDesign and oversee efficacy and TAS studies in partnership with Clinical Development Sciences, Biostatistics, Regulatory Affairs, and external research facilities to support global regulatory approvals. • Analyze and interpret study data with support from Data Management, Medical Writing, and internal/external reviewers; prepare documentation and support submissions and presentations to regulatory authorities and scientific forums.
Pharmavise CorporationClinical Research Manager Pharmavise CorporationClinical Research ManagerIndianapolis, MARemoteE-Verify Participation: Pharmavise Consulting Corporation participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S. If E-Verify cannot confirm that you are authorized to work, Pharmavise is required to give you written instructions and an opportunity to contact Department of Homeland Security (DHS) or Social Security Administration (SSA) so you can begin to resolve the issue. The CRM manages cross-functional teams, monitors timelines and budgets, and acts as the primary liaison between investigators, CROs, vendors, and internal stakeholders.
Integrated Resources, IncSr. Quality Specialist Integrated Resources, IncSr. Quality SpecialistIndianapolis, INRemoteContractorDescription: The Computer System Quality Assurance Team provides quality oversight of business enterprise technology within the Pharmaceutical Services Group (PSG) of ***, ensuring compliance to regulations for computer system validation (CSV) and assurance with respect to data integrity, computer system lifecycle activities, and adherence to PSG QMS systems. Our desired candidate has a Bachelors Degree, or higher, in Science, Engineering or QA/Regulatory related course of study, has direct pharmaceutical experience (QA, QC, or Regulatory Affairs), and is an effective collaborator who can develop an internal strategic network while working remotely.
Compass Pathways(Senior) Medical Science Liaison (Great Lakes) Compass Pathways(Senior) Medical Science Liaison (Great Lakes)Indianapolis, INRemoteMSL) at Compass Pathways is a core member of the Medical Affairs organization, connecting the company's science with the broader mental health and neuroscience community, helping to shape medical strategy, and supporting the continued development of Compass Pathways' work in treatment-resistant depression (TRD) and post-traumatic stress disorder (PTSD). The ideal candidate is passionate about a field-based role establishing themselves as a key point of scientific contact, actively engaging in high-quality scientific exchange and gathering insights from the field on emerging research, changes in the treatment landscape, and evolving approaches to care.
Pharmavise CorporationClinical Data Manager Pharmavise CorporationClinical Data ManagerIndianapolis, MARemotePharmavise Consulting Corporation participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S. If E-Verify cannot confirm that you are authorized to work, Pharmavise is required to give you written instructions and an opportunity to contact Department of Homeland Security (DHS) or Social Security Administration (SSA) so you can begin to resolve the issue. This role collaborates closely with cross-functional teams, including Clinical Operations, Biostatistics, Medical Writing, and Regulatory Affairs, to support timely and compliant study execution.
ElancoSenior Research Scientist ElancoSenior Research ScientistIndianapolis, INFull timeYour Role: Senior Research Scientist - Farm Animal Clinical Development, Vaccines and Infectious Diseases As a Senior Research Scientist, you will be an integral member of the Farm Animal Clinical Development team, dedicated to bringing innovative vaccines and therapeutics to our customers. Reporting to the Clinical Team Lead, you will have the opportunity to conduct and coordinate global clinical programs, from inception through to approval, that directly contribute to Elanco's mission of enriching life by progressing the health of animals.
ElancoSenior Research Scientist - Clinical Operations ElancoSenior Research Scientist - Clinical OperationsIndianapolis, INFull timeIn this role, you will provide veterinary oversight to support clinical development and product registration, ensuring studies are conducted in alignment with FDA CVM, USDA APHIS CVB, EPA (where applicable), VICH GL9 Good Clinical Practice, and pharmacovigilance requirements, while safeguarding animal welfare and study integrity. • Strong ability to interpret clinical and safety data, combined with excellent verbal and written communication skills to translate complex medical concepts to investigators, pet owners, and cross-functional partners.
AES CorporationNERC Operations Sr Analyst, East AES CorporationNERC Operations Sr Analyst, EastUS, Indianapolis, IN$83,000–$99,450 / yearThe NERC Operations Analyst plays a critical part in upholding the reliability and security of the Bulk Electric System by working closely with the Team Leader and various teams to embed best practices in reliability and regulatory compliance across the organization. AES is proudly ranked #1 globally in renewable energy sales to corporations, and with $12.7B in revenues in 2023, we have the resources and expertise to make a significant impact as we provide electricity to 25 million customers worldwide.
AES CorporationNewNERC Operations Sr Analyst, Central AES CorporationNERC Operations Sr Analyst, CentralUS, Indianapolis, IN$83,000–$99,450 / yearThe NERC Operations Analyst plays a critical part in upholding the reliability and security of the Bulk Electric System by working closely with the Team Leader and various teams to embed best practices in reliability and regulatory compliance across the organization. AES is proudly ranked #1 globally in renewable energy sales to corporations, and with $12.7B in revenues in 2023, we have the resources and expertise to make a significant impact as we provide electricity to 25 million customers worldwide.
AES CorporationProject Controls | Capital Projects | Cost Analyst | SAP AES CorporationProject Controls | Capital Projects | Cost Analyst | SAPUS, Indianapolis, INpreferred) Understanding of fixed assets accounting Strong problem-solving skills Ability to analyze financial data and prepare financial reports, statements, and projections Ability to deal with fast-paced, constantly changing environments with high levels of complexity and ambiguity Ability to work in a collaborative manner with business leaders and to balance priorities and achieve critical deadlines; capable of independent and critical, forward-looking and preemptive thought analysis. Supports Digital Strategy and represents PMO for the implementation of Work Management system, Copperleaf system, and supports the implementation of Robotic Processing Automation and SAP enhancements for process efficiencies (SAP IM-PS / SAP PM / SAP MM / SAP FI / ERPRPC - FIORI) Oversee portfolio to optimize investment decisions, control costs, and ensure alignment with enterprise strategy.
GovCIONewConfiguration Management Associate (Remote) GovCIOConfiguration Management Associate (Remote)Indianapolis, INRemoteWhat You Can ExpectInterview & Hiring ProcessIf you are selected to move forward through the process, here's what you can expect:During the Interview ProcessVirtual video interview conducted via video with the hiring manager and/or teamCamera must be onA valid photo ID must be presented during each interviewDuring the Hiring ProcessEnhanced Biometrics ID verification screeningBackground check, to include:Criminal history (past 7 years)Verification of your highest level of educationVerification of your employment history (past 7 years), based on information provided in your applicationEmployee PerksAt GovCIO, we consistently hear that meaningful work and a collaborative team environment are two of the top reasons our employees enjoy working here. Update routines using approved VistA tools (KIDS Utilities, ^XINDEX) and submit Data Dictionary changes to the DBA.Validate ICR usage, submit new or updated ICR requests, and coordinate HL7 messaging reviews for impacted components.
HealthDriveMobile Podiatrist HealthDriveMobile PodiatristAvon, IndianaOverview: HealthDrive is currently seeking a Podiatrist, to work Part-Time (3 days/week), covering nursing facilities in the Western Indianapolis area(work available in the Frankfort, Sheridan, Crawfordsville, and Danville areas). HealthDrive delivers on-site podiatry, optometry, dentistry, audiology, and behavioral health services to residents in long-term care, skilled nursing and assisted living facilities.
Otsuka America PharmaceuticalNewManaged Market Liaison- Pacific NW Otsuka America PharmaceuticalManaged Market Liaison- Pacific NWIndianapolis, INCreate and grow widespread relationships with regional/local payer decision makers and maintain a comprehensive understanding of assigned managed care accounts, the healthcare system, and trends, the interconnect of the key decision makers and payer landscape and access challenges. Account responsibilities include ecosystem level payers: Medicaid, Insurers, Specialty Pharmacy, Integrated Delivery Networks (IDNs), Pharmacy Benefit Managers (PBMs) and Federal Healthcare (Veterans Administration regional sites, Military Treatment Facilities sites).
ElancoManager, Marketing Operations and Process Excellence & Enablement ElancoManager, Marketing Operations and Process Excellence & EnablementIndianapolis, INFull timeKey Skills: Demonstrated expertise and primary ownership of complex business processes, with a proven track record of promoting optimization and governance; Strong project management and cross-functional leadership skills, with a proven ability to guide large-scale, complex initiatives and influence diverse stakeholders. Manage the execution of large-scale content transformation and technology initiatives, such as Digital Asset Management (DAM), text assets, and QR code management, to develop solutions that impact results across the marketing function.
Danaher CorporationNewAdvanced Technician Quality Control- Inspection - 6:00am - 2:30pm Danaher CorporationAdvanced Technician Quality Control- Inspection - 6:00am - 2:30pmIndianapolis, INEnter quality data into the proper database to demonstrate the inspection has been successfully completed; record non-conformance data in the applicable database and provide feedback to appropriate personnel when required and electronically transfer material according to its acceptance or rejection status. At Beckman Coulter Life Sciences, we know time is the most critical facet in the laboratory today: time to get life-saving therapies to patients faster; reclaiming time by automating tedious manual workflows; and saving time spent addressing erroneous or complex results.
Danaher CorpSr. Technician Quality Control- Inspection - 6:00am - 2:30pm Danaher CorpSr. Technician Quality Control- Inspection - 6:00am - 2:30pmIndianapolis, INIt would be a plus if you also possess previous experience in: Experience setting up and running a CMM machine would be a bonus (not required) Beckman Coulter Life Sciences, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. At Beckman Coulter Life Sciences, we know time is the most critical facet in the laboratory today: time to get life-saving therapies to patients faster; reclaiming time by automating tedious manual workflows; and saving time spent addressing erroneous or complex results.
Thermo Fisher Scientific IncNewStaff Program Manager (Transplant Diagnostics) Thermo Fisher Scientific IncStaff Program Manager (Transplant Diagnostics)Fishers, INOur distributed team of more than 100,000 colleagues delivers an unrivaled combination of innovative technologies, purchasing convenience and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services and Patheon. Key Responsibilities: Lead core teams and conduct regular project meetings (including capturing meeting minutes and assigning action owners), supervise assigned deliverables, develop timelines, and provide project updates and reports to senior leadership.
Eli Lilly and CoTSMS Lab Advisor Eli Lilly and CoTSMS Lab AdvisorLebanon, IN$129,000–$209,000 / yearOur 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). As a TSMS Lab Advisor at Eli Lilly and Company, you will be a key contributor to our Technical Services and Manufacturing Science (TSMS) team, providing expert scientific and technical guidance within our laboratory operations.
** Bristol-Myers Squibb **Req Number:** R1598658 **Updated:** 2026-01-29 04:20:23.209 UTC **Location:** Indianapolis-INBristol Myers SquibbVice President, General Manager & Site Head, Indianapolis ** Bristol-Myers Squibb **Req Number:** R1598658 **Updated:** 2026-01-29 04:20:23.209 UTC **Location:** Indianapolis-INBristol Myers SquibbVice President, General Manager & Site Head, IndianapolisIndianapolis, IN$330,690–$389,050 / yearThe Site Head will be responsible for setting strategic direction for the relevant radiopharmaceutical manufacturing departments, in alignment with corporate goals, RayzeBio Product Development and Operations and objectives, including commercialization of our products while maintaining highly productive clinical operations. Responsible for establishing and driving a culture of collaboration and alignment between various functions and departments within RayzeBio, Bristol Myers Squibb and the site, ensuring operational performance with aggressive continuous improvement in productivity and implementation of innovative technologies while ensuring that major strategic objectives are met.
** Bristol-Myers Squibb **Req Number:** R1598658 **Updated:** 2026-01-29 04:20:23.190 UTC **Location:** Indianapolis-INBristol Myers SquibbVice President, General Manager & Site Head, Indianapolis ** Bristol-Myers Squibb **Req Number:** R1598658 **Updated:** 2026-01-29 04:20:23.190 UTC **Location:** Indianapolis-INBristol Myers SquibbVice President, General Manager & Site Head, IndianapolisIndianapolis, IN$330,690–$389,050 / yearThe Site Head will be responsible for setting strategic direction for the relevant radiopharmaceutical manufacturing departments, in alignment with corporate goals, RayzeBio Product Development and Operations and objectives, including commercialization of our products while maintaining highly productive clinical operations. Responsible for establishing and driving a culture of collaboration and alignment between various functions and departments within RayzeBio, Bristol Myers Squibb and the site, ensuring operational performance with aggressive continuous improvement in productivity and implementation of innovative technologies while ensuring that major strategic objectives are met.
Eli Lilly and CoDigital Innovation & Technology Strategy - Global PK/PD & Pharmacometrics Eli Lilly and CoDigital Innovation & Technology Strategy - Global PK/PD & PharmacometricsIndianapolis, IN$177,000–$308,000 / yearClinical Operations, Statistics, Regulatory Affairs) to ensure seamless AI integration across R&D and serve as the primary voice for AI strategy within PK/PD leadership and governance forums • Grow and implement organisational change strategies to drive AI adoption, including training programs, champion networks, and upskilling resources that address resistance and build organisational capability in AI/ML methodologies • Define success metrics and track value creation for digital/technology initiatives, maintaining a portfolio of use cases with clear ROI documentation and preparing executive-level cases and communications • Establish relationships with external partners (e.g. 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).