The Regulatory Affairs Manager will lead efforts to ensure compliance with regulatory requirements for products within the personal care and beauty industry. To excel as a Regulatory Affairs Manager, ...
read moreThe Regulatory Affairs Manager will lead efforts to ensure compliance with regulatory requirements for products within the personal care and beauty industry. Job Title: Regulatory Affairs Manager. To ...
read moreRepresent Regulatory Affairs on Insmeds Commercial Review Committee providing coordination and meeting facilitation. Minimum of 1 years relevant work experience in Regulatory Affairs. Reviews current ...
read moreSenior Manager/Associate Director, Global Regulatory Affairs, Labeling Strategy. The Global Regulatory Labeling Strategy Sr Manager/Associate Director will be responsible for leading the development a...
read moreSenior Manager of Regulatory Affairs, you will play a key role in the regulatory strategy and submission activities related to ANDAs and 505(b)(2) applications for sterile injectables, specifically th...
read moreSenior Manager of Regulatory Affairs, you will play a key role in the regulatory strategy and submission activities related to ANDAs and 505(b)(2) applications for sterile injectables, specifically th...
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 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 moreSenior Manager/Associate Director, Global Regulatory Affairs, Labeling Strategy. The Global Regulatory Labeling Strategy Sr Manager/Associate Director will be responsible for leading the development a...
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 moreSenior Manager of Regulatory Affairs, you will play a key role in the regulatory strategy and submission activities related to ANDAs and 505(b)(2) applications for sterile injectables, specifically th...
read moreSenior Manager of Regulatory Affairs, you will play a key role in the regulatory strategy and submission activities related to ANDAs and 505(b)(2) applications for sterile injectables, specifically th...
read moreSenior Manager of Regulatory Affairs, you will play a key role in the regulatory strategy and submission activities related to ANDAs and 505(b)(2) applications for sterile injectables, specifically th...
read moreSenior Manager of Regulatory Affairs, you will play a key role in the regulatory strategy and submission activities related to ANDAs and 505(b)(2) applications for sterile injectables, specifically th...
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 moreMinimum of 1 years relevant work experience in Regulatory Affairs. Represent Regulatory Affairs on Insmeds Commercial Review Committee providing coordination and meeting facilitation. Reviews current ...
read moreRepresent Regulatory Affairs on Insmeds Commercial Review Committee providing coordination and meeting facilitation. Minimum of 1 years relevant work experience in Regulatory Affairs. Reviews current ...
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 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 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 moreYears of Experience Required in Regulatory Affairs or related field. Ensure efficient regulatory review of artworks to ensure compliance with regulatory standards. Validate the text and regulatory men...
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 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 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 moreBachelor or Masters Degree in a scientific area (Degree in Pharmacy/Regulatory Affairs is preferred). Responsible for maintaining and updating various regulatory databases to ensure accuracy of inform...
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 of Regulatory Affairs - Southern CT. Ability to accurately complete and analyze regulatory data, produce accurate and detailed written reports.
Perform 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 moreWork with CMC cross-functional teams and Regulatory Affairs teams. PREREQUISITES BS/BA degree in Scientific Discipline (master's or higher preferred) with + years in the pharmaceutical industry, prefe...
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 moreOur 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...
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