This role manages logistics for medical and patient conferences, overseeing planning from inception to conclusion. Responsibilities include vendor management, budget allocation, venue selection, and onsite support. The ideal candidate must thrive in a fast-paced environment and work effectively with minimal supervision.

The Director, Quality Systems and Compliance will lead the Quality Systems program, ensuring compliance with cGMP/ICH/FDA/EU regulations. Responsibilities include managing quality metrics, overseeing audits, maintaining quality systems, and ensuring inspection readiness. The position requires strong leadership skills and the ability to implement quality processes.

The Director of Document and Training Management at Pliant Therapeutics is responsible for leading the GxP document management and training systems. This role involves managing the Veeva QualityDocs program, overseeing document workflows and personnel training, and driving compliance with industry standards and regulations. The director will also develop quality metrics, support inspection readiness, and enhance training processes.