Senior Regulatory Affairs Specialist Jobs

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 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...

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 Senior Regulatory Affairs Specialist is responsible for directing and coordinating the implementation of regulatory compliance programs as required by government agencies. They ensure that product...

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

The Senior Specialist, Regulatory Affairs at Baxter is responsible for implementing global regulatory strategies, acquiring and maintaining marketing authorizations for products, and communicating reg...

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

The Senior Regulatory Affairs Specialist is responsible for planning and executing global regulatory activities for Medtronic's surgical robotic device portfolio. This includes obtaining and maintaini...

The Senior Regulatory Affairs Specialist is responsible for supporting design control compliance for assigned products and executing regulatory strategies for clearance/approval. They also handle comp...

The Senior Regulatory Affairs Specialist is responsible for developing strategies for worldwide regulatory approval, preparing submissions, and ensuring compliance with regulatory requirements...

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

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 Senior Specialist, Regulatory Affairs at Baxter Healthcare Corporation is responsible for developing and executing regulatory strategies to support market life-cycle management and new product dev...

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 Senior Specialist - Regulatory Affairs, Animal Health is responsible for maintaining pesticide registrations, FDA submission support, and preparation of regulatory reports. They will also lead and...

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 Regulatory Affairs Specialist will be responsible for preparing and managing regulatory applications, technical files, and FDA reports. They will also act as a subject matter expert on new product...

The Regulatory Affairs Specialist will be responsible for supporting international registrations and maintaining certificates to support product registrations. They will collaborate with marketing in...

The Regulatory Affairs Specialist will be responsible for preparing and managing regulatory applications, technical files, and FDA reports. They will also act as a subject matter expert on new product...

The Regulatory Affairs Specialist will be responsible for supporting international registrations and maintaining certificates to support product registrations. They will collaborate with marketing in...

The Senior Regulatory Affairs Specialist (Medical Devices) is responsible for developing and executing regulatory strategies, reviewing promotional materials, and maintaining regulatory clearance for...

The Medical Affairs Specialist is responsible for driving and managing clinical documentation to support marketing and regulatory needs, providing clinical expertise, and ensuring compliance with glob...

Provides messaging to market leadership for internal communication as it relates to Public and Government Affairs initiatives.

The Public Affairs Specialist will provide public affairs and strategic communications support for a DoD client, including developing and implementing various deliverables such as articles, press rele...

Work closely with clients to formulate a filing strategy prior to the start of any activities to ensure the studies are designed fulfilling the FDA's requirements and tailored to the clients' needs. C...