Regulatory jobs in Springfield, IL

Job DescriptionAssists and supports the organization in complying with, as well as the ongoing preparation, testing and monitoring of conformance to, the requirements of government regulations and/or regulatory agencies.Responsibilities+ Performs evaluation of internal operations, controls, communications, risk assessments and maintenance of documentation as related to regulatory compliance and...

A global pharmaceutical company in Springfield, Illinois is seeking a Vice President of Regulatory Affairs Oncology. In this role, you will lead regulatory strategies and submissions, ensuring compliance with FDA regulations. The ideal candidate has extensive experience in Oncology and biopharmaceutical regulations, along with proven leadership capabilities. A competitive salary and benefits...

A healthcare technology company based in the United States is seeking a Regulatory Strategist to collaborate cross-functionally and manage regulatory submissions crucial for their innovative projects. The ideal candidate has at least 10 years of experience in the regulatory field, particularly in IVD or medical devices, with a strong understanding of FDA processes. The role offers competitive...

Job Summary Responsible for leading the quality and compliance for the Supplier Quality Program (Audits and Supplier Quality). Set organizational priorities, oversee resource utilization and develop operational plans and policies. Job Description A high number of candidates may make applications for this position, so make sure to send your CV and application through as soon as...

Bausch + Lomb (NYSE/TSX: BLCO) is a leading global eye health company dedicated to protecting and enhancing the gift of sight for millions of people around the worldfrom the moment of birth through every phase of life. Our mission is simple, yet powerful: helping you see better, to live better.Our comprehensive portfolio of over 400 products is fully integrated and built to serve our customers...

A leading pharmaceutical company in Springfield, Illinois, is seeking an Associate Director of Regulatory Intelligence. This role involves leading regulatory intelligence efforts, ensuring compliance with regulations, and managing a team. The ideal candidate will have a master's degree in a related field and significant regulatory affairs experience. This position offers competitive compensation...

Your Journey at Crowe Starts Here:At Crowe, you can build a meaningful and rewarding career. With real flexibility to balance work with life moments, you're trusted to deliver results and make an impact. We embrace you for who you are, care for your well-being, and nurture your career. Everyone has equitable access to opportunities for career growth and leadership. Over our 80-year history,...

A leading public accounting firm is seeking an Assistant General Counsel for Litigation and Regulatory Affairs in Springfield, IL. The successful candidate will manage litigation, advise on regulatory investigations, and support risk management strategies. A Juris Doctor and a minimum of 10 years' experience are required. This position offers a salary range of $149,400 to $317,100 per year and...

Our mission is to detect cancer early, when it can be cured. We are working to change the trajectory of cancer mortality and bring stakeholders together to adopt innovative, safe, and effective technologies that can transform cancer care. We are a healthcare company, pioneering new technologies to advance early cancer detection. We have built a multi-disciplinary organization of scientists,...

A global pharmaceutical company is seeking an experienced Associate Director of Regulatory Affairs to manage regulatory submissions and compliance for oncology products. The ideal candidate will have extensive experience in regulatory affairs within the biopharmaceutical industry and a strong understanding of FDA regulations. This role includes leading a team and ensuring adherence to regulatory...

Job DescriptionOverviewWe are seeking a highly experienced sales and business development professional to drive growth across Commercial, Real-World Evidence (RWE), Clinical, Regulatory, and Safety research services within pharmaceutical and biotechnology organizations. This role is responsible for identifying, developing, and closing complex, large-scale engagements by aligning client needs with...

Bausch + Lomb (NYSE/TSX: BLCO) is a leading global eye health company dedicated to protecting and enhancing the gift of sight for millions of people around the world from the moment of birth through every phase of life. Our mission is simple, yet powerful: helping you see better, to live better.Our comprehensive portfolio of over 400 products is fully integrated and built to serve our customers...

Job DescriptionAbout the RoleOracle Health Data Intelligence is entering a high-impact phase of MDR (Medical Device Regulation) readiness and regulatory transformation . Over the next year, HDI must execute a large volume of technical documentation, risk management activities, and engineering design updates required for compliance across our AI-enabled population health platform.To support these...

Bausch + Lomb (NYSE/TSX: BLCO) is a leading global eye health company dedicated to protecting and enhancing the gift of sight for millions of people around the worldfrom the moment of birth through every phase of life. Our mission is simple, yet powerful: helping you see better, to live better.Our comprehensive portfolio of over 400 products is fully integrated and built to serve our customers...

Sumitomo Pharma Co., Ltd. is a global pharmaceutical company based in Japan with key operations in the U.S. (Sumitomo Pharma America, Inc.), Canada (Sumitomo Pharma Canada, Inc.) and Europe (Sumitomo Pharma Switzerland GmbH) focused on addressing patient needs in oncology, urology, women's health, rare diseases, psychiatry & neurology, and cell & gene therapies. With several marketed products in...

Sumitomo Pharma Co., Ltd., is a global pharmaceutical company based in Japan with operations in the U.S. (Sumitomo Pharma America, Inc.), focused on addressing patient needs in oncology, urology, women's health, rare diseases, cell & gene therapies and CNS. With several marketed products and a diverse pipeline of early‑to‑late‑stage investigational assets, we aim to accelerate discovery,...

Job Description About the Role: At a time when global technological developments and healthcare regulations are occurring and changing at an unprecedented rate, the success of large, complex global health companies requires regulatory leaders who are deeply steeped in the public and private levers that impact this industry. To remain competitive in this rapidly changing landscape, organizations...

Job Description Modern healthcare demands integrated solutions. At Oracle Health, we connect patients, providers, payers, and public health organizations with AI-powered, interoperable solutions that help streamline data exchange, surface actionable insights, and drive operational efficiencies across the care continuum. As an Interoperability Regulatory Strategist, you will monitor and evaluate...

Job DescriptionThis role is dedicated to understanding healthcare regulatory requirements (such as HIPAA, HITRUST, FDA, etc.) and guiding cross-functional teams to systematically integrate those requirements into our SDLC and release management practices. You will work to ensure our processes generate the required documentation, evidence, and compliance packages-ready for both internal use and...

Job DescriptionOracle Health Data Intelligence (HDI) is hiring a Principal Technical Program Manager - Operations to lead key strategic and operational initiatives across the organization. This is a highly visible role where you'll report directly to the Director of Operations as a right-hand leader and help scale programs, headcount, tooling, and processes across operations, engineering,...