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Associate Director, Regulatory Affairs CMC

AbbVie Inc.Florham ParkNew
On-site Full-time

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Experience Level

Mid to Senior

Qualifications

Proven experience in regulatory affairs, specifically within CMC. Strong knowledge of FDA regulations and guidance related to drug development. Excellent communication and leadership skills. Ability to work collaboratively in a fast-paced environment. Advanced degree in life sciences or a related field is preferred.

About the job

The Associate Director of Regulatory Affairs CMC at AbbVie will lead and manage the regulatory strategy for chemistry, manufacturing, and controls (CMC) submissions. This role is crucial in ensuring compliance with regulatory requirements while facilitating the smooth progression of our innovative products through the development lifecycle.

About AbbVie Inc.

AbbVie is a global, research-based biopharmaceutical company committed to developing innovative medicines that address some of the world's most complex health issues. We strive to make a remarkable impact on patients' lives through our dedication to science and improving patient outcomes.

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