NewRegulatory Affairs Manager CYNET SYSTEMSRegulatory Affairs ManagerIndianapolis, IN$48–$53 / hourTemporaryContractorPart timeAs a nationally and locally certified Minority Business Enterprise (MBE), Cynet Systems is committed to helping organizations build high-performing teams while empowering professionals to grow rewarding careers. 3-5 years of experience with PhD degree, 5-7 with Masters degree and 6-8 years with Bachelor degree in the field of IVDs, Medical devices, Pharma, or Biopharmaceutical with significant experiences in Regulatory Affairs or equivalent.
NewSenior Medical Science Liaison Rare Epilepsies- North Central LundbeckSenior Medical Science Liaison Rare Epilepsies- North CentralIndianapolis, IN$180,000–$220,000 / yearStrategic Scientific Engagement & Insight Generation: Establishes and sustains deep, longitudinal scientific partnerships with Key Opinion Leaders (KOLs), Centers of Excellence, and investigators working in rare epilepsies. This role serves as a strategic pre-launch scientific partner to external experts and internal stakeholders, generating high-quality, actionable insights that inform evidence strategy, disease education, portfolio decision-making, and launch readiness.
Global Regulatory Lead, Regulatory Strategy - Global Regulatory Affairs - Infectious Disease/Vaccine Eli Lilly and CompanyGlobal Regulatory Lead, Regulatory Strategy - Global Regulatory Affairs - Infectious Disease/VaccineUs, Indiana$169,500–$248,600 / yearOur 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). 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.
NewAssociate Director - Global Regulatory Affairs - Product Communications Eli Lilly and CoAssociate Director - Global Regulatory Affairs - Product CommunicationsIndianapolis, IN$132,000–$193,600 / yearOur 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). Organization Overview: The purpose of the Associate Director, Global Regulatory Affairs - Product Communications role is to provide leadership and influence to deliver accurate, balanced, and substantiated product and disease communications for assigned assets.
NewRegulatory Affairs Project Manager F. Hoffmann-La Roche LtdRegulatory Affairs Project ManagerIndianapolis, IN$84,600–$157,200 / yearIn this position, you will have a role in working with internal and Roche affiliates for a wide array of innovative medical diagnostic products for researchers, physicians, patients, hospitals, laboratories, and blood banks in high-profile demographic regions, specifically in APAC, LATAM, the Middle East, and Africa. Provide support to currently marketed products, e.g., review engineering changes, labeling, product changes, and documentation for compliance and for changes requiring regulatory agency approval, as per international regulatory requirements.
Associate Director, Regulatory Affairs – Biologics ElancoAssociate Director, Regulatory Affairs – BiologicsGreenfield, INFull timeExperienced product Regulatory Affairs professional with 5+ years of direct RA experience, ideally biologics/vaccines or CMC, who has owned regulatory strategy, submissions and agency interactions and is either Indianapolis-based or clearly willing to relocate. 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.
Associate Director, Regulatory Affairs - Biologics Elanco Animal Health IncAssociate Director, Regulatory Affairs - BiologicsIndianapolis, INElanco 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. The ideal candidate brings experience in biologics, vaccines, biotechnology, or pharmaceutical regulatory affairs and has supported regulatory strategy, health authority interactions, and regulatory submissions.
Director, Product Compliance And Regulatory Affairs Delta Faucet CompanyDirector, Product Compliance And Regulatory AffairsIndianapolis, IN$121,300–$190,630 / yearE-Verify is an Internet based system operated by the Department of Homeland Security (DHS) in partnership with the Social Security Administration (SSA) that allows participating employers to electronically verify the employment eligibility of their newly hired employees in the United States. Collaborate with Engineering, Quality, Product, Sourcing, Legal, Manufacturing, and other collaborators to identify, assess, and mitigate product compliance risks in new product launches, engineering changes, systems, and business processes.
Director, Product Compliance and Regulatory Affairs Delta Faucet CoDirector, Product Compliance and Regulatory AffairsIndianapolis, IN$121,300–$190,630 / yearE-Verify is an Internet based system operated by the Department of Homeland Security (DHS) in partnership with the Social Security Administration (SSA) that allows participating employers to electronically verify the employment eligibility of their newly hired employees in the United States. Collaborate with Engineering, Quality, Product, Sourcing, Legal, Manufacturing, and other collaborators to identify, assess, and mitigate product compliance risks in new product launches, engineering changes, systems, and business processes.
NewRegulatory Affairs Manager I Integrated Resources, IncRegulatory Affairs Manager IIndianapolis, IN3-5 years experience with PhD degree, 5-7 with master s degree and 6-8 years with Bachelor degree in the field of IVDs/Medical devices/Pharma/Biopharmaceutical with significant experiences in Regulatory Affairs or equivalent. Proactively creates unique/innovative regulatory strategies and influencing approaches to avoid regulatory obstacles and accelerate worldwide approvals.
Director, Product Compliance And Regulatory Affairs Masco Corp.Director, Product Compliance And Regulatory AffairsIndianapolis, IN$121,300–$190,630 / yearE-Verify is an Internet based system operated by the Department of Homeland Security (DHS) in partnership with the Social Security Administration (SSA) that allows participating employers to electronically verify the employment eligibility of their newly hired employees in the United States. Collaborate with Engineering, Quality, Product, Sourcing, Legal, Manufacturing, and other collaborators to identify, assess, and mitigate product compliance risks in new product launches, engineering changes, systems, and business processes.
Director, Product Compliance and Regulatory Affairs Masco CorpDirector, Product Compliance and Regulatory AffairsIndianapolis, IN$121,300–$190,630 / yearE-Verify is an Internet based system operated by the Department of Homeland Security (DHS) in partnership with the Social Security Administration (SSA) that allows participating employers to electronically verify the employment eligibility of their newly hired employees in the United States. Collaborate with Engineering, Quality, Product, Sourcing, Legal, Manufacturing, and other collaborators to identify, assess, and mitigate product compliance risks in new product launches, engineering changes, systems, and business processes.
NewRegulatory Affairs Manager Actalent IncRegulatory Affairs ManagerIndianapolis, INThe position coordinates and compiles regulatory documents and submissions, develops and executes global regulatory strategies, and partners closely with internal and external stakeholders to navigate evolving regulatory environments. This role leads regulatory affairs activities for a defined portfolio of products, ensuring timely regulatory approvals, successful product registrations, and ongoing lifecycle maintenance across multiple global markets.
NewRegulatory Affairs Manager I_CO TalentBurst, Inc.Regulatory Affairs Manager I_COIndianapolis, IN$50–$53 / hourThe efficiency and the success of the Regulatory activities and strategies are maintained by clear agreements with other functions, stakeholders and external partners (authorities, companies, NBs etc). Contributes to or leads projects with an understanding of how business functions, systems, processes, and data management are connected and essential to achieving digitalization and strategic goals.
Regulatory Affairs Specialist, EHS, North America Henry Schein IncRegulatory Affairs Specialist, EHS, North AmericaIN$56,604–$88,443 / yearDevelop and deliver employee environmental, health, and safety (EHS) awareness and training programs to ensure compliance with applicable federal, state, and international regulations, including OSHA, OSHA State Plans (e.g., Cal/OSHA), DOT, IATA, IMO, and EPA requirements. Proficient in Microsoft Office applications, including PowerPoint, and experienced with project management methodologies and tools commonly used in the medical device or pharmaceutical industries.
NewSenior Manager Regulatory Affairs - Systems & Software F. Hoffmann-La Roche LtdSenior Manager Regulatory Affairs - Systems & SoftwareIndianapolis, IN$126,800–$235,000 / yearYou will have the opportunity to navigate complex and evolving regulatory areas-including integrated instrument systems, software, cybersecurity, automation, connectivity, and digital technologies-while helping translate innovation into regulatory strategies that enable successful product development and commercialization. This role offers significant visibility, autonomy, and opportunity to influence, making it ideal for an experienced regulatory professional who enjoys solving complex problems, shaping strategy, and seeing their work directly contribute to the future of pathology and patient care.
Manager, Regulatory Affairs Project Management Bristol Myers SquibbManager, Regulatory Affairs Project ManagementIndianapolis, IN$134,505–$162,988 / yearBased on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day. The Manager, Regulatory Project Management is responsible for planning, executing, and driving regulatory submissions and regulatory project activities across clinical and nonclinical programs.
NewRegulatory Affairs Manager BC ForwardRegulatory Affairs ManagerIndianapolis, IN$45–$50 / hourFull timeThe ideal candidate will have strong experience in global regulatory submissions, IVDs/medical devices/biopharma regulations, and regulatory change control and a proven ability to secure and maintain product approvals across multiple regions while driving cross-functional alignment and timely registration outcomes . With delivery centers and offices across North America and India, we take pride in building long-term relationships and delivering excellence through innovation, collaboration, and integrity.
Regulatory Affairs Manager, Companion Diagnostics RocheRegulatory Affairs Manager, Companion DiagnosticsIndianapolis, IndianaYou have 3-5 years experience with PhD degree, 5-7 with Masters degree and 6-8 years with Bachelor degree in the field of IVDs/Medical devices/Pharma/Biopharmaceutical with significant experiences in Regulatory Affairs. You understand the structure, key roles and responsibilities of external customers/stakeholders and communicate timely and effectively the needs of external customers/stakeholders.
Regulatory Affairs Manager, Companion Diagnostics F. Hoffmann-La Roche LtdRegulatory Affairs Manager, Companion DiagnosticsIndianapolis, IN$106,100–$197,000 / yearYou have 3-5 years experience with PhD degree, 5-7 with Masters degree and 6-8 years with Bachelor degree in the field of IVDs/Medical devices/Pharma/Biopharmaceutical with significant experiences in Regulatory Affairs. You understand the structure, key roles and responsibilities of external customers/stakeholders and communicate timely and effectively the needs of external customers/stakeholders.