Regulatory Affairs Specialist Jobs

The Regulatory Affairs Specialist at Alcon is responsible for ensuring compliance with FDA and other regulatory requirements, supporting global registrations efforts, and providing high-quality regula...

The Regulatory Affairs Specialist collaborates with teams and management to ensure compliance with global regulations and standards for safety products...

The Senior Regulatory Affairs Specialist will support Stryker's Joint Replacement Division in ensuring regulatory compliance for medical devices. They will assess changes to devices, develop regulator...

The Senior Regulatory Affairs Specialist is responsible for authoring regulatory submissions and technical files for US markets, as well as providing guidance and advice on regulatory requirements. Th...

Collaboratively interface with a variety of levels on significant matters, often requiring the coordination of activity across organizational units.

The Senior Specialist - Regulatory Affairs provides tactical support for system development, maintenance, and monitoring initiatives within the GRACS Innovation & Information Management organization...

Principal Regulatory Affairs Specialist responsible for developing and implementing regulatory strategies for medical devices in the Joint Replacement Division. This role involves authoring regulatory...

Lead and collaborate with cross functional partners (Marketing, Sales, Quality, Finance, Operations and others) to ensure regulatory and labeling compliance to protect consumer health, company and bra...

The Principal Regulatory Affairs Specialist is a lead regulatory/technical role focused on supporting the compliance and safety of products for Burt's Bees cosmetic business, including over-the-counte...

The Regulatory Affairs Specialist II is responsible for assisting in the preparation of regulatory submissions, reviewing protocols and reports, and maintaining compliance with regulatory requirements...

Principal Specialist Regulatory Affairs responsible for directing and overseeing the preparation of documentation to support high quality regulatory submissions in the medical device industry...

The Regulatory Affairs Specialist III, Regulatory Intelligence and Environmental Compliance is responsible for coordinating global product regulatory intelligence and ensuring compliance with environm...

The Principal Regulatory Affairs Specialist - Cardiac Surgery (hybrid) is responsible for developing strategies for worldwide governmental approval to introduce new products to market, maintain existi...

The Specialist Regulatory Affairs role at Abbott Park, IL involves providing support for the regulatory department to ensure efficient and compliant business processes and environment. The role requir...

The Senior Regulatory Affairs Specialist is responsible for developing strategies for global approvals of spinal cord stimulation systems, maintaining existing products, and providing regulatory suppo...

The Principal Regulatory Affairs Specialist - Global Regulatory Strategy and Advocacy position at Medtronic Diabetes involves formulating and advocating for innovative global regulatory strategies for...

The Principal Regulatory Affairs Specialist - Manufacturing Transfers is responsible for developing and implementing medical device regulatory strategies to obtain timely approvals from worldwide regu...

Foreign Affairs Specialist responsible for leading and coordinating aviation-related activities with U.S. Government agencies, foreign civil aviation authorities, and international organizations...

Senior Regulatory Affairs Specialist responsible for coordinating and preparing regulatory submissions in the US, EU, and Canada.

The Foreign Affairs Specialist serves as a point of contact for activities in a geographic region, coordinating activities of individual countries and making recommendations to senior managers. They a...

The Foreign Affairs Specialist serves as a principle coordinator for activities in a geographic region, making recommendations on technical assistance, international training, bilateral agreements, an...

The Software Regulatory Affairs Specialist (Senior Staff Level) is responsible for setting global regulatory strategy for new product development, with a focus on software, AI, machine learning, conne...

The Regulatory Affairs Specialist II is responsible for preparing regulatory submissions for new or modified medical devices in domestic and international markets. They provide guidance on regulatory...

The Senior Regulatory Affairs Specialist will provide strategic and operational support to partners for global market access. They will work closely with company partners as well as internal business...

The Regulatory Affairs Manager is responsible for providing technical and strategic feedback for regulatory decisions associated with medical device software, digital health, and cybersecurity. They w...