Associate Director, CMC Regulatory Affairs - Tarrytown, NY

This Regulatory Affairs Specialist contractor position supports US Beverages Regulatory Affairs initiatives. · ...

Join us in pioneering breakthroughs in healthcare. · Sustainably. · Analyzes the requirements and prepares product related regulatory submissions. · ...

This Regulatory Affairs Specialist contractor position supports US Beverages Regulatory Affairs initiatives. · The primary focus of this position is to support graphic refreshes of the Beverages portfolio which includes the development of the nutrition and ingredient label declar ...

Support the Senior Director in developing and executing regional regulatory strategies for QOL. · Contribute to providing strategic oversight and leadership to the regulatory team, · ensuring alignment with company objectives and regional regulatory requirements. ...

The Regulatory Affairs Label Reviewer will report to the Senior Manager, Regulatory Affairs and, · under the direction and guidance of the Head of Regulatory Affairs,to ensure regulatory compliance of labeling and associated materials · of Prestige marketed products. · ...

The Sr. Regulatory Affairs Manager will be responsible for developing and implementing global regulatory strategies to drive pipeline development and global launch excellence. · Develop and oversee the implementation of strategies for new product development and life cycle design ...

The Director Regulatory Affairs will provide leadership on global regulatory activities for assigned products. · Provide interpretation of regulatory authorities feedback policies and guidelines. · Lead development of regulatory strategic plans either directly or through reports ...

+The Director Regulatory Affairs will provide leadership on global regulatory activities for the assigned products. · This role might be for you if: You bring strong understanding of US FDA and international pharmaceutical guidance, regulations, drug development process, and indu ...

This Regulatory Affairs Specialist contractor position supports US Beverages · Regulatory Affairs initiatives. · ...

US Agent for all products responsible for communication between the FDA and manufacturing sites. · ...

This Job Description shows the most important duties of the Quality Management & Regulatory Affairs Specialist at Herbstreith & Fox Inc. · ...

This Job Description shows the most important duties of the Quality Management & Regulatory Affairs Specialist at Herbstreith & Fox Inc. · ...

The position will require a basic understanding and application of US Food and Drug Administration labeling regulations to ensure the accuracy and regulatory compliance of ingredient statements, nutrition facts, allergen declarations, and claims. · ...

+The Senior Manager, Regulatory Affairs will report to the Global Regulatory Liaison (GRL) and provides support to the GRL in all aspects of regulatory affairs related to the development of novel therapeutics including quality, preclinical and clinical areas of drug development a ...

The Regulatory Affairs Specialist will support US Beverages Regulatory Affairs initiatives by collaborating with Regulatory Leads on assigned projects. The primary focus of this role is to support beverage portfolio graphic refreshes by developing and reviewing compliant nutritio ...

The Senior Manager, Regulatory Affairs will report to the Global Regulatory Liaison and provides support in all aspects of regulatory affairs related to drug development and compliance with regulations. · Coordinate the preparation and submission of global regulatory submissions ...

This Regulatory Affairs Specialist contractor position supports US Beverages · Rarely to monitor interpret and ensure compliance with US regulations today and into the future. · B.S Degree in Food Science or equivalent as minimum. · 1-2 years regulatory affairs experience in foo ...

This Regulatory Affairs Specialist contractor position supports US Beverages Regulatory Affairs initiatives. · ...

+The Senior Manager, Regulatory Affairs will report to the Global Regulatory Liaison (GRL) and provides support to the GRL in all aspects of regulatory affairs related to the development of novel therapeutics including quality, · preclinical and clinical areas of drug development ...

The Senior Manager position within the Regulatory Affairs department requires the ability to apply clinical development knowledge in concert with experienced understanding of advertising and promotion regulations/guidance to the development of key product messages presented in Bi ...

As Associate Director you will lead the development and execution of global CMC regulatory strategies for the hematology and oncology portfolios. You will guide regulatory activities across development stages, mentor CMC Regulatory Affairs (RA) staff supporting cross-functional a ...