The Association for Accessible Medicines (AAM), is seeking a Director of Sciences and Regulatory Affairs to join its team. This is an invaluable opportunity to work at a dynamic, growing trade association at the center of some of the most important science and regulatory affairs policy issues facing our industry. The working environment is high-energy, fast-paced and the culture is entrepreneurial.
This position provides an opportunity to identify and manage science and regulatory affairs projects; as well as, develop public comments, policy papers and other materials in support of AAM’s member company’s strategic goals and mission.
The role will also monitor and track trends and developments in the generic industry and provide analysis and consultation to AAM staff and member companies. Additionally, this role will keep members up-to-date on the development of relevant draft regulations, guidelines, and procedures of associated U.S. Government Agencies.
Candidates shall have 5+ years of professional regulatory experience in an FDA role or a pharmaceutical industry organization specific to regulatory compliance, quality and/or manufacturing inspection/investigation experience. Additionally, the candidate shall have experience with and understanding of the relationship and interconnectivity between the various FDA offices that oversee the review and approval of generic drug applications.
The Association for Accessible Medicines improves access to safe, quality, effective medicine. AAM is located in Gallery Place/Chinatown. For more information about the Association for Accessible Medicines visit www.accessiblemeds.org. A full job description can be found at https://accessiblemeds.org/careers.
Please email resume and salary expectations (required) to: