Travere Therapeutics is seeking an Associate Director, Technical Operations QC to lead Quality Control activities in a GMP environment. The candidate will oversee specifications, batch release, and collaborate across teams to ensure compliance with regulatory standards.
This role requires at least 8 years of experience in analytical operations, particularly in biologics, and the ability to adapt in a dynamic, fast-paced environment. A commitment to delivering innovative solutions for patients with rare diseases is essential.
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