Browse 36 exciting jobs hiring in Regulatory Affairs now. Check out companies hiring such as Telix Pharmaceuticals (AMER), Radiant Industries, Scholar Rock in Columbus, San Jose, Columbus.
Telix Pharmaceuticals is hiring a Senior Project Manager to own end-to-end delivery of a late-stage therapeutics program, coordinating cross-functional teams and stakeholders across a global organization.
Serve as Chief of Staff to the Chief Nuclear Officer, translating regulatory strategy into action and aligning licensing, policy, and external engagement to advance Radiant's mission.
Scholar Rock is hiring a Senior Director of Patient Marketing to own U.S. patient and caregiver strategy and execution for apitegromab’s launch and commercialization in spinal muscular atrophy.
Lead global regulatory and materials compliance for Evolv's hardware products, owning certifications, radiation safety officer duties, and cross-functional compliance processes to enable scalable international growth.
Technical regulatory leader sought to author and drive FDA regulatory strategy and submissions for AI/ML-enabled SaMD at a fast‑moving digital health company.
Experienced licensing engineer to support NRC interactions, develop licensing application content, and help execute regulatory strategy for X-energy reactor technology.
Astranis seeks an experienced Market Access Manager to secure international authorizations and drive regulatory strategy for its growing satellite fleet.
AbbVie is hiring a Senior Manager to lead US advertising and promotion regulatory activities for immunology products, ensuring compliance and strategic alignment across cross-functional teams.
AbbVie seeks an Associate Data Analyst in Tempe to manage vigilance reporting, regulatory submissions, and stakeholder communications for pharmaceutical and device complaints.
ARK Diagnostics is hiring a Regulatory Affairs Specialist II to own international product registrations, support submissions (e.g., 510(k), De Novo, IVDR), and maintain regulatory compliance at its Fremont, CA facility.
Experienced regulatory professional needed to drive U.S. regulatory strategy and submissions for complex robotic, electromechanical, and SaMD products at a leading surgical robotics company.
PowerLines is hiring a part-time Government Partnerships Advisor to develop bipartisan policymaker relationships and accelerate the organization’s policy impact on utility regulation and energy affordability.
ARK Diagnostics is seeking an experienced Senior Clinical Affairs Specialist to lead clinical validation studies, specimen acquisition, and regulatory documentation for IVD assays at the Fremont, CA facility.
Lead quality strategy and design-control activities for next-generation robotic-assisted surgical products at a market-leading medical device company.
Perplexity seeks a technically excellent, interdisciplinary engineer to drive strategic AI policy, compliance, IP, and operations initiatives directly with senior leadership.
Lead client-facing Medical Information operations and a small team at EVERSANA, ensuring compliant, scientifically balanced medical responses, strong client relationships, and staff proficiency.
ARK Diagnostics is hiring a Regulatory Affairs Specialist II to manage international device registrations, prepare regulatory submissions (including 510(k), De Novo, and IVDR technical documentation), and support lifecycle compliance for IVD and medical device products.
Neuralink seeks a high-autonomy Clinical Program Manager to architect and deliver complex human clinical trial programs for cutting-edge brain-computer interface technology.
Protective Insurance Company is hiring a Product Compliance Analyst II to draft and manage compliant insurance forms and filings for the Employee Benefits Division in a remote role.
Work with Voltus' Energy Markets team to manage market operations, optimize data workflows, and build analytical tools that enable customers to monetize distributed energy resources.
CSL Behring is hiring an experienced Global Regulatory Affairs CMC Team Lead to lead CMC strategy, manage submissions and represent the company in regulatory interactions for biological and non-biological product portfolios.
Experienced regulatory/quality professional needed to maintain QMS activities, drive CAPA and change control, and support audit and regulatory documentation for a growing medical device company in New York State.
Senior regulatory leader needed to lead Sobi’s Global Advertising & Promotion team, drive regulatory strategy and FDA interactions, and own the global review process for promotional and corporate materials.
Lead US regulatory strategy and cross-functional review for advertising and promotion at AbbVie to ensure compliant, effective communication of products.
Aurora seeks a Senior Manager of Government Relations to lead federal advocacy, stakeholder engagement, and regulatory outreach from Washington, D.C. to support the company’s autonomy and transportation policy goals.
Senior physician leader sought to define and execute Artera's clinical strategy, build high-value data partnerships, and drive adoption of AI-enabled precision oncology diagnostics.
Senior clinical leader needed to define and execute a global clinical evidence strategy that drives regulated product development, submissions, and lifecycle evidence for a medical technology organization.
Be part of AbbVie's two-year Physician’s Development Program as an Associate Medical Director, rotating through core R&D functions to build clinical development expertise in therapeutic areas such as Neuroscience, Oncology, and Endocrinology.
Lead AbbVie’s US advertising and promotion regulatory strategy for Eye Care products, managing a small team and partnering cross-functionally to ensure compliant, competitive promotional activities.
Lead strategic client relationships and operational delivery for regulated clinical research services, driving onboarding, retention, and growth while partnering across functions to ensure service excellence.
Airbnb is hiring a Senior Manager, Public Policy to lead local and state advocacy in Texas, building partnerships with officials and stakeholders to advance fair regulations for hosts and communities.
AbbVie is hiring a detail-oriented Senior Administrative Assistant to provide high-level executive and administrative support to the Global Regulatory Affairs Strategy team in Irvine on a hybrid schedule.
Lead global post-market clinical strategy for a medical device portfolio, driving surveillance, evidence generation, and lifecycle decision-making at the executive level.
Lead large-scale, cross-functional product development programs at Intuitive to deliver next-generation minimally invasive surgical platforms from concept to commercial launch.
Senior leader needed to shape and lead permitting, stakeholder engagement, and community relations for a major Western Colorado resource development, ensuring regulatory readiness and long-term social license.
Lead development and execution of HCP in-office marketing materials and field communications for AbbVie's Parkinson's Disease launch, partnering closely with sales, medical, regulatory, and agency teams.
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