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Associate Director, CMC Project Manager

Summary:
We seek an Associate Director, CMC Project Manager skilled in pharmaceutical late phase drug development and commercialization to support project management of our Chemistry Manufacturing and Control (CMC) activities in conjunction with internal subject matter experts and external project managers from Tricida’s CMOs.  The Associate Director will be responsible for planning and on-time completion of a variety of drug manufacturing and testing activities including the management of deliverables and ongoing risk mitigation.  The Associate Director will report to the Senior Director, CMC Project Management.  The successful candidate must possess a strong technical understanding of the inter-disciplinary nature of drug development, preferably demonstrated with previous drug development and commercialization experience.  The position will collaborate closely with cross-functional team members, including process chemistry, drug product manufacturing, analytical chemistry, regulatory and clinical operations, to ensure timely manufacturing of drug substance and drug product, regulatory agency updates, and supply of clinical trial material.

Responsibilities Include:

Experience & Skills:

Competitive Compensation and Benefits include:  Medical, Dental, and Vision Coverages, Life, AD&D, Disability, 401(k), Flexible Spending Plan, and Stock Options.  15 vacation days per year and 11 paid holidays per year, which includes 1 floating holiday.

To apply for this position, please send resumes to jobs@tricida.com and indicate Job Code 310.125

 EOE