Key ResponsibilitiesExecute regulatory strategies and compile submissions such as IND, CTA, and major submissions like (s)NDA and MAALead the preparation of Agency interaction documents and co-chair c...
read moreThe Global Regulatory Affairs Manager will lead the team tasked with supporting product submissions globally. You will coordinate regulatory documents, ensuring that submissions are timely and regulat...
read moreThe Global Regulatory Affairs Manager will lead the team tasked with supporting product submissions globally. You will coordinate regulatory documents, ensuring that submissions are timely and regulat...
read moreThe Regulatory Affairs Manager will play a crucial role in ensuring our products comply with all applicable regulations and standards. Minimum of 5-7 years of regulatory affairs experience in the cosm...
read moreThe Global Regulatory Affairs Manager will lead the team tasked with supporting product submissions globally. You will coordinate regulatory documents, ensuring that submissions are timely and regulat...
read moreThe Regulatory Affairs Manager will play a crucial role in ensuring our products comply with all applicable regulations and standards. Minimum of 5-7 years of regulatory affairs experience in the cosm...
read moreValidate the text and regulatory mentions of packaging in French and English to ensure regulatory compliance of finished products. Years of Experience Required in Regulatory Affairs or related field. ...
read moreThe Regulatory Affairs Manager will play a crucial role in ensuring our products comply with all applicable regulations and standards. Minimum of 5-7 years of regulatory affairs experience in the cosm...
read moreThe Regulatory Affairs Manager will play a crucial role in ensuring our products comply with all applicable regulations and standards. Minimum of 5-7 years of regulatory affairs experience in the cosm...
read moreThis role will be within Global Regulatory Affairs (GRA) and will report to the Sr Director, Labeling, Policy and Intelligence. The Global Regulatory Labeling Strategy Sr Manager/Associate Director wi...
read moreThe Global Regulatory Labeling Strategy Sr Manager/Associate Director will be responsible for leading the development and maintenance of global labeling documents (e. This role will be within Global R...
read moreThe Regulatory Affairs Associate Manager supports Colgate’s Oral Care and Personal Care divisions. Minimum 5 years of experience in regulatory affairs within the consumer goods or pharmaceutical indus...
read moreThe Regulatory Affairs Associate Manager supports Colgate’s Oral Care and Personal Care divisions. Manage regulatory activities to ensure compliance with FDA’s Modernization of Cosmetic Regulatory Act...
read moreManager, Regulatory Affairs integrates and applies knowledge of US regulatory guidelines and federal regulations governing pharmaceutical drug development to all aspects of Our Client’s ’s drug develo...
read moreManager, Regulatory Affairs integrates and applies knowledge of US regulatory guidelines and federal regulations governing pharmaceutical drug development to all aspects of Our Client’s ’s drug develo...
read moreThe Regulatory Manager also develops and implements regulatory strategies to support innovation projects and works in anticipation of regulatory developments with the potential to affect the current p...
read moreThe Regulatory Manager also develops and implements regulatory strategies to support innovation projects and works in anticipation of regulatory developments with the potential to affect the current p...
read moreThe Regulatory Affairs Manager is responsible for the development and execution of global regulatory strategy and tactical planning for assigned microbiology on market products or those products in de...
read moreManager/Associate Director, Regulatory Strategist is responsible for the assigned branded programs and all strategic decisions to include providing regulatory pathway for the development, preview of c...
read morePerform the compliance activities of the portfolio to determine regulatory impact and associated submission requirement for clinical and commercial regulatory filings with country specific regulatory ...
read moreThis manager will serve as liaison between DDG brand holder and HQ regulatory team on the DDG medical devices regulatory compliance evaluation and registration ensuring all the products for registrati...
read morePerform the compliance activities of the portfolio to determine regulatory impact and associated submission requirement for clinical and commercial regulatory filings with country specific regulatory ...
read moreThis manager will serve as liaison between DDG brand holder and HQ regulatory team on the DDG medical devices regulatory compliance evaluation and registration ensuring all the products for registrati...
read morePerform the compliance activities of the portfolio to determine regulatory impact and associated submission requirement for clinical and commercial regulatory filings with country specific regulatory ...
read moreThe Manager will collaborate closely with the Director and VP of Regulatory Affairs, focusing on tasks such as regulatory submissions, initiating and reviewing change controls, and managing labeling a...
read moreThe Manager will collaborate closely with the Director and VP of Regulatory Affairs, focusing on tasks such as regulatory submissions, initiating and reviewing change controls, and managing labeling a...
read moreThe Sr GPRM works under limited supervision of the regulatory affairs (RA) program lead to develop and implement the global regulatory strategy for program(s) through development, registration and pos...
read moreThe Manager, Regulatory Affairs is responsible for the overall daily planning, developing, implementation, and coordinating the Hospital’s regulatory and accreditation compliance program. The Manager,...
read moreThe Manager, Regulatory Affairs reports into the Director/Associate Director Regulatory Affairs and is based in Pine Brook, New Jersey. Manages team and leads Regulatory Associates and/or Senior Regul...
read moreThe Manager, Regulatory Affairs is responsible for the overall daily planning, developing, implementation, and coordinating the Hospital’s regulatory and accreditation compliance program. The Manager,...
read moreThe Manager, Regulatory Affairs reports into the Director/Associate Director Regulatory Affairs and is based in Pine Brook, New Jersey. Manages team and leads Regulatory Associates and/or Senior Regul...
read moreRegulatory Affairs Senior Manager is responsible for leading the regulatory strategy and managing the regulatory compliance in Personal Care and Cosmetics. Lead and enhance the regulatory program to e...
read moreRegulatory Affairs Senior Manager is responsible for leading the regulatory strategy and managing the regulatory compliance in Personal Care and Cosmetics. This position will report directly to the Gl...
read moreThe 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...
read moreThe 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...
read moreThe 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...
read moreOur client is currently seeking a Senior Manager, Regulatory Affairs Strategy. Regulatory Affairs Certified is a plus. Provides regulatory strategic support and guidance to project teams.
Our client is currently seeking a Senior Manager, Regulatory Affairs Strategy. Regulatory Affairs Certified is a plus. Responsible for developing and implementing short and long term global regulatory...
read moreThe Regulatory Affairs Manager will create, evaluate and execute domestic and/or international regulatory tasks related to the following: global submissions, technical file compilation, facility regis...
read moreThe Regulatory Affairs Manager will create, evaluate and execute domestic and/or international regulatory tasks related to the following: global submissions, technical file compilation, facility regis...
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