The 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...

The 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...

The 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...

The 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...

The 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...

The 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...

The Manager Regulatory Affairs, Pharma US will manage and execute the US regulatory affairs for Aptar Pharma across the 3 divisions (mainly RX in short term) to strengthen Aptar Pharma leadership in d...

The 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...

The 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...

The 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...

The 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...

The 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...

The 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...

The 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...

The 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...

Bachelor or Masters Degree in a scientific area (Degree in Pharmacy/Regulatory Affairs is preferred). Preferred experience in reviewing, authoring, or managing components of regulatory submissions. Ab...

Manager, 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...

Manager, 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...

The Regulatory Affairs Manager manages the staff and daily activities of Regulatory Affairs, provides training, support, and guidance as it pertains to the overall functions of the Department. Assists...

The Regulatory Affairs Manager manages the staff and daily activities of Regulatory Affairs, provides training, support, and guidance as it pertains to the overall functions of the Department. Assists...

Manager of Regulatory Affairs - Southern CT. Ability to accurately complete and analyze regulatory data, produce accurate and detailed written reports.

Regulatory Affairs Certification (RAC) is a plus. Demonstrated expertise in preparing CMC sections of regulatory submissions (, INDs, NDAs, BLAs, MAAs, IMPDs) and interacting with global health author...

Prepare and submit CTAs within the EU Clinical Trial Integrated System (CTIS) and MHRA Integrated Regulatory Submission (IRAS) submission portals in accordance with regulatory requirements, using Subm...

Prepare and submit CTAs within the EU Clinical Trial Integrated System (CTIS) and MHRA Integrated Regulatory Submission (IRAS) submission portals in accordance with regulatory requirements, using Subm...

Supervise, review and approval of labeling for marketed products Track applications through FDA reviewing divisions Work with project associate on compilation of information and supportive documentati...

Supervise, review and approval of labeling for marketed products Track applications through FDA reviewing divisions Work with project associate on compilation of information and supportive documentati...

We expect the Manager, Regulatory Affairs CMC to join a growing team and provide support to interpret the current, approved and planned clinical regulatory landscape by contributing to the regulatory ...

We expect the Manager, Regulatory Affairs CMC to join a growing team and provide support to interpret the current, approved and planned clinical regulatory landscape by contributing to the regulatory ...

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 ...

The 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...

The 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...

The 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...

Work with CMC cross-functional teams and Regulatory Affairs teams. May be responsible for the global regulatory evaluation of CMC change controls with supervision. Develop and maintain knowledge of re...

Work 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...

Manages team and leads Regulatory Associates and/or Senior Regulatory Associates in regulatory activities associated with planning, authoring, compiling and submitting highest-quality regulatory submi...

The 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...

The 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...

The 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...

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...

The Senior Regulatory Affairs Manager ensures regulatory compliance of company’s US cosmetic, OTC, dietary supplement, and device products from brief through launch in North America. Over 8 years of R...