Regulatory Affairs Jobs

Senior Regulatory Affairs Specialist at Medtronic driving regulatory compliance and strategic submissions to advance healthcare technology.

Smith+Nephew seeks a Senior Manager, Evidence Evaluation to lead clinical documentation and regulatory compliance initiatives for orthopedic and robotic medical devices in a fully remote role.

Lead strategic business development efforts as VP, Business Development, Compliance at EVERSANA to grow revenue and foster key partnerships in the life sciences compliance market.

Protective looks for an Associate Counsel with policy expertise to advance government affairs through analysis, monitoring, and stakeholder coordination in a hybrid role based in Washington D.C. or Birmingham, AL.

Regulatory Affairs Specialist needed to support new product development and regulatory submissions at a top medical device company in Sunnyvale, CA.

Organon is seeking an Associate Principal Scientist to lead regulatory CMC strategies and submissions for clinical and marketed pharmaceutical products.

Leading regulatory strategy and submissions for clinical development programs at a premier global clinical research organization.

Lead GeneDx’s government affairs efforts as VP, driving federal and state policy strategy to support innovation in genomic medicine and healthcare access.

Lead regulatory strategies and oversight for a growing pharmaceutical portfolio as Executive Director of Regulatory Affairs in Jersey City.

Lead Toyota’s regulatory compliance and certification initiatives for North American on-road vehicles as a Principal Engineer in the Carbon Neutrality & Regulatory Affairs Division.

Lead regulatory compliance and risk management efforts as Deputy Compliance Officer & DMLRO at Crypto.com, a global cryptocurrency platform.

Noah Medical seeks a Staff Design Quality Engineer (ME/EE) to lead quality assurance efforts supporting cutting-edge medical robotics development.

CorDx seeks an experienced Regulatory Affairs Manager in San Diego to lead regulatory compliance and submissions for cutting-edge medical diagnostic devices.

The Associate Regulatory Affairs Manager at CorDx will support regulatory submissions and compliance efforts for medical device and diagnostic products in San Diego.

An experienced MSL Manager role at Vantive, leading medical affairs for Acute Therapies with a focus on ECCO2R, engaging healthcare professionals to advance vital organ care.

Experienced medical information leader needed to develop and execute medical information strategies for Cogent Biosciences’ oncology and rare disease product launches.

A Senior Manager, Pharmacovigilance Scientist role at Cogent Biosciences focusing on safety monitoring and signal management across clinical trials in a fast-paced biotech setting.

Lead strategic market access and reimbursement initiatives for Gilead’s viral hepatitis therapies, driving optimal patient coverage through cross-functional collaboration.

Lead strategic communications and change management for AbbVie's Regulatory Affairs team in a hybrid onsite role focused on business and technology initiative success.