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TypeFull-Time
Our Regulatory Affairs consultants help clients understand and address regulatory challenges at critical stages of product development, commercialization and distribution. This high performing team ...
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Our Regulatory Affairs consultants help clients understand and address regulatory challenges at critical stages of product development, commercialization and distribution. This high performing team ...
Our client, a leading medical device company, is currently seeking an ambitious Manager of Regulatory Affairs and Compliance to help lead their team. This is a unique opportunity for a highly ...
Key job responsibilities As Manager, International Regulatory Affairs & Licensing, you will work with engineering, business, legal, and public policy professionals to execute the licensing strategy ...
Represent Regulatory Affairs on project teams and closely collaborate with multidisciplinary teams to identify submission requirements and define timelines to ensure on-time delivery of high-quality ...
The position will work in close collaboration with the Regulatory Affairs CMC DP Team to implement and coordinate all aspects of regulatory activities as needed to support the global development of ...
The Manager/Senior Manager for Regulatory Affairs Global Labeling will function as the regulatory expert for labeling on the Global Regulatory Affairs (GRA) and other teams to ensure that regulatory ...
The Manager will represent Regulatory Affairs on cross-functional project teams, will provide input to the project team, will lead authoring and preparation of annual reporting, and will manage ...
The purpose of the Executive Director, R&D Quality Partner, Regulatory Affairs and Global Labeling is to provide strategic and operational leadership for Regulatory Affairs and Global Labeling ...
As an Senior Director working on the Global Regulatory Affairs Oncology team, you will be empowered to provide leadership and development to global regulatory leads to ensure innovative and robust ...
CMC Regulatory Affairs Directors are a core member of our cross-functional Regulatory Strategy, Pharmaceutical and Global Supply Teams. Working in partnership with the technical functions, CMC ...
The Regulatory Affairs - CMC Manager independently manages all regulatory CMC aspects of Bausch Health Company Pharmaceutical products throughout their lifecycle with minimum supervision. This ...
The Principal Regulatory Affairs Specialist works independently in preparing and managing regulatory submissions and interacts with regulatory agencies/health authorities/authorized representatives ...
As Associate Director/ Director - Global Regulatory Affairs, Precision Medicine & Digital Health you will manage/lead/be responsible to ensure the development of appropriate global and/or regional ...
The Regulatory Affairs team, a sub-department of Global Government Relations, engages in balanced advocacy with regulators and policymakers, understanding and providing thought leadership on how ...
The State Government & Regulatory Affairs Rep III is responsible for leading, developing and maintaining state government and regulatory agency and non-governmental organization relationships in all ...
The VP of Regulatory Affairs will lead development of regulatory strategies through cross-functional teams to ensure expedited and successful advancement of innovative products to approval. This ...
If so, this Regulatory Affairs Management Manager could be an ideal opportunity to explore. As a Regulatory Affairs Management Manager, you will be responsible for regulatory submissions ...
ERM is seeking an experienced Principal Regulatory Affairs and Product Stewardship Consultant with significant regulatory expertise to play a key role in growing our Product Stewardship and ...
Manager/Sr. Manager, Regulatory Affairs Reporting to the Chief Regulatory Officer or designee, you'll be responsible for managing and implementing the regulatory development plan for assigned ...
Regulatory Affairs CMC Specialist/Sr. SpecialistThis position is primarily responsible for coordinating the preparation, review, and compilation of CMC filings in support of commercial applications ...
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