Regulatory Affairs Manager BC Forward AsymblRegulatory Affairs ManagerIndianapolis, Indiana$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 I_CO - Contract TalentBurst, Inc.Regulatory Affairs Manager I_CO - ContractIndianapolis, 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 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.
Family Nurse Practitioner/Physician Assistant - Up to $5K Sign On Bonus Fast Pace HealthFamily Nurse Practitioner/Physician Assistant - Up to $5K Sign On BonusTerre Haute, INPosting Title: Family Nurse Practitioner/Physician Assistant - Up to $5K Sign On Bonus 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. They 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.
NewResearch Principal Engineer I- #26-21710 US Tech Solutions, Inc.Research Principal Engineer I- #26-21710Warsaw, INCollaborates across design, process engineering, manufacturing, quality, regulatory, corporate, and site teams to advance research initiatives and support broader neuro-related project needs. Serves as a scientific subject matter expert and advisor to cross-functional teams including R&D, Marketing, Sales, Clinical Affairs, and Regulatory Affairs.
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.
Associate 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.
Regulatory Affairs Analyst Consultant ClinChoiceRegulatory Affairs Analyst ConsultantBrazil, INEnsures proper submission and approvals for market licenses including new registrations, changes and timely renewals, and establishment registrations, organizing and balancing a multitude of projects simultaneously. Must have 1-2 years experience at least working in Regulatory Environment (and/or training or equivalent combination of education and experience), preparing submissions for Brazilian Health Authorities and a successful track record.
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.
Regulatory Affairs Specialist Actalent IncRegulatory Affairs SpecialistIN$50–$55 / hourWe are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing winner for both client and talent service. The specialist supports regulatory strategy, documentation, and communication activities to ensure products comply with applicable regulations and can be successfully introduced and maintained in the market.
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.
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.
Regulatory 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.
Regulatory Affairs Specialist LanceSoft IncRegulatory Affairs SpecialistWarsaw, IN$52–$56.02 / hourAbility to learn and stay abreast of regulations pertinent to medical devices, biologics, drugs and combination products as needed, based on functional area. Provides regulatory direction to development project teams as a core team member; develops regulatory strategy for new products.
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.
Regulatory 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.
Regulatory Affairs Specialist ICONMA, LLCRegulatory Affairs SpecialistWarsaw, IN$50.41–$54.45 / hourAbility to learn and stay abreast of regulations pertinent to medical devices, biologics, drugs and combination products as needed, based on functional area. Provides regulatory direction to development project teams as a core team member; develops regulatory strategy for new products.