Regulatory Affairs Jobs
Browse 106 exciting jobs hiring in Regulatory Affairs now. Check out companies hiring such as AbbVie, Gilead, Veeva Systems in Mesa, Knoxville, Miami.
AbbVie's USAP Standards Team is hiring a PharmD student intern to support FDA advertising and promotion review, reporting, and process improvement initiatives during the 2026 summer program.
Experienced Regulatory Affairs professional needed to lead preparation and coordination of regional regulatory submissions and labeling for investigational and commercial products at Gilead in Foster City.
Experienced regulatory systems consultant needed to lead MedTech clients through enterprise deployments of Veeva RIM and related regulatory information management processes.
Foresight Diagnostics seeks a Senior Specialist, Regulatory Affairs to lead US regulatory strategy and submissions for next-generation sequencing-based IVD products while partnering cross-functionally through development and lifecycle management.
Care Access is hiring a Regulatory Operations Specialist to manage site-level IRB and regulatory activities for U.S. clinical trials in a remote, fast-paced environment.
Senior physician to lead oncology clinical development programs, driving trial design, safety oversight and medical strategy across GSK's oncology portfolio.
An experienced nonclinical regulatory toxicologist is needed to lead cross-functional safety strategy and regulatory interactions for immunology therapeutic projects at Novartis.
EVERSANA seeks an experienced Director of Quality Assurance & Regulatory Compliance to lead QA/RA strategy and operations across regulated life‑sciences services and ensure full GxP and regulatory adherence.
Gilead seeks an experienced Sr Director to lead CMC Regulatory Affairs digital transformation, driving strategy, vendor programs, and implementation of AI/ML and structured-content solutions to accelerate submissions and improve regulatory outcomes.
Nasdaq is hiring a Government Relations Specialist in Washington, D.C. to manage federal policy engagement, PAC operations, stakeholder outreach, and event logistics in support of corporate and market objectives.
ORIC Pharmaceuticals seeks a Regulatory Affairs Manager to drive timely, compliant regulatory submissions and support clinical oncology programs from its San Diego office.
Support Stryker’s Regulatory Affairs team in Bloomington this summer by assisting with regulatory data collection, submission preparation, and documentation process improvements.
A strategic pharmacy regulatory leader is needed to drive state advocacy and Board of Pharmacy engagement for CVS Health’s regional regulatory initiatives.
Experienced medical communications leader needed to drive client strategy, cross-functional execution, and account growth for Klick Health’s Scientific Innovation and Medical Communications department.
Provide strategic regulatory leadership for U.S. advertising, promotion, and medical materials for high-priority products at Novartis' East Hanover site.
ActiGraph is hiring a Senior Compliance Specialist to lead QMS and regulatory compliance activities across product development, post-market surveillance, and audits for their medical-grade wearable solutions.
Lead global contact center and medical information operations at Moderna to ensure compliant, high-quality engagement for patients and healthcare professionals while scaling capabilities for a growing pipeline.
Lead Clear Channel Outdoor’s Miami real estate and public affairs operations to maximize asset value, manage entitlements, and advance regulatory and community relationships.
Lead strategic regulatory labeling activities for AbbVie’s US/EU products, coordinating cross-functional teams to ensure compliant, consistent and optimized product labeling.
Regeneron is hiring an Associate Director of Strategy & Operations to lead strategic planning, communications, and resource management across RA, Global Patient Safety, and Development Quality.
Lead regulatory strategy, licensing, and stakeholder engagement to secure approvals that enable Starlink service launches and growth across assigned international markets.
Guardant Health is hiring a Senior Regulatory Affairs Manager to lead U.S. regulatory strategy and submissions for Oncology IVD/CDx products, guiding products from development through post-market compliance.
Lead regulatory strategy and submissions for PROCEPT BioRobotics' surgical robotics products, guiding projects from development through market approval and post-market activities.
DeepHealth seeks a hands-on QA/RA Project Manager to drive quality, regulatory readiness, and cross-functional delivery for medical device software and digital health products in a fully remote role.
Allucent seeks a seasoned VP, CMC (contractor) to lead regulatory strategy, CMC development, and global Health Authority interactions to accelerate life-changing therapies.
Serve as an experienced regulatory leader providing CMC strategy, hands-on submission support, and Health Authority engagement to advance drug, biologic, and device programs for Allucent clients.
AbbVie is hiring a Marketing Manager I/II to lead gastroenterology peer-to-peer speaker bureau programs, vendor relationships, and field training to drive franchise growth and sales-force effectiveness.
At Rain, own and operationalize licensing strategies across U.S. Money Transmitter Licenses and international regulatory regimes to enable compliant global growth.
Sanford Health is hiring a Research Compliance Specialist in Sioux Falls to manage IRB submissions, maintain clinical trial documentation, and ensure regulatory compliance for clinical research studies.
Senior leader responsible for defining and executing AbbVie's clinical development strategy across Japan and China, aligning regional programs with global priorities and regulatory requirements.
Senior-level regulatory leader needed to shape and execute global regulatory strategy for a late-stage biologic asset at argenx, supporting submissions and commercialization readiness.
AbbVie's Regulatory Affairs organization is looking for an experienced Associate Director to lead US Advertising & Promotion strategy and cross-functional teams in a hybrid or remote capacity.
Lead international regulatory strategy for advertising and promotion at AbbVie, ensuring global compliance while enabling strategic brand communications for marketed and pipeline products.
Senior medical affairs leader needed to drive oncology/hematology strategy, clinical evidence generation, and cross-functional medical support for AbbVie's product portfolio in a hybrid San Francisco role.
Lead regulatory strategy and submissions for device and combination products at AbbVie to ensure timely global approvals and compliance.
Senior legal leader needed to build and run HopSkipDrive's legal and compliance function, advising the executive team and scaling legal infrastructure across a rapidly growing marketplace business.
Lead device and combination product regulatory strategy and submissions at AbbVie to support timely approvals and market access.
Emory University is hiring a Regulatory Specialist II to manage IRB submissions, regulatory compliance, and trial documentation for a portfolio of clinical studies with hybrid work flexibility.
AbbVie seeks specialist physicians (MD/DO) for a two-year Physician Development Program based in North Chicago to develop clinical research and medical affairs expertise through rotational assignments across R&D functions.
Lead and scale ecoATM's Regulatory Operations function to ensure local licensing and compliance across the kiosk network while driving process automation and regulatory strategy.
AbbVie seeks early-career physician specialists to participate in a two-year onsite Physician Development Program in North Chicago, rotating through core R&D functions as Associate Medical Directors.
A two-year onsite rotational program at AbbVie’s North Chicago HQ that develops specialist physicians into Associate Medical Directors through cross-functional R&D rotations in oncology and related therapeutic areas.
Experienced oncology medical affairs leader needed to drive scientific strategy, clinical evidence generation, medical education, and safety oversight for AbbVie’s hematology/oncology programs on a hybrid schedule based in Mettawa, IL.
AbbVie's two-year Physician Development Program prepares recent M.D./D.O. specialists for R&D careers through rotational assignments across clinical development, safety, regulatory and medical affairs at the North Chicago headquarters.
AbbVie’s two-year Physician Development Program prepares graduating fellows for careers in R&D by providing onsite rotations and mentorship across clinical development, safety, medical affairs and regulatory functions.
AbbVie seeks M.D./D.O. candidates (recent residency or fellowship graduates) for a two-year, onsite Physician Development Program in Neuroscience and related therapeutic areas, entering as Associate Medical Directors to gain cross-functional R&D experience.
Adtalem seeks a politically savvy Senior Manager, Issues & Public Affairs to drive rapid-response advocacy, stakeholder engagement, and regulatory intelligence across the enterprise.
AbbVie is hiring Associate Medical Directors for a two-year onsite Physician’s Development Program in North Chicago, focused on developing fellows into R&D medical leaders across clinical development, safety, regulatory, and medical affairs.
Senior regulatory leader sought to drive FDA and global regulatory strategy and submissions for innovative IVD and multi-cancer early detection products based in Menlo Park, CA.
Provide executive-level administrative support to Visa's SVP and Chief Counsel for Global Risk and Regulatory Affairs, handling complex calendars, travel, confidential communications, and meeting materials.
How much do regulatory affairs jobs pay?
Below 50k*
0
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50k-100k*
14
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Over 100k*
68
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Top companies hiring for regulatory affairs jobs
- AbbVie 15
- American Express 5
- Veeva Systems 2
- Foresight Diagnostics Inc. 2
- Novartis 2
- Gilead 2
- SpaceX 2
