Qualifications
Advanced degree in Life Sciences, Chemistry, or a related field.Minimum of 8 years of experience in Regulatory Affairs, particularly in CMC.Strong understanding of regulatory guidelines and submission processes.Excellent communication and leadership skills.Proven ability to work collaboratively in a team environment.
About the job
AbbVie is seeking a dedicated and experienced Associate Director for our Regulatory Affairs CMC team, located in Florham Park, New Jersey. In this pivotal role, you will lead regulatory strategy and provide guidance on CMC (Chemistry, Manufacturing, and Controls) submissions to ensure compliance with regulatory standards.
Your expertise will contribute significantly to our mission of delivering innovative therapies to patients worldwide. You will work closely with cross-functional teams to facilitate efficient product development and approval processes.
About AbbVie Inc.
AbbVie is a global biopharmaceutical company committed to developing advanced therapies that address some of the world's most complex health challenges. With a focus on innovation and patient care, we strive to make a meaningful impact in the lives of individuals and communities worldwide.