Seeking a Director of PV Quality Management to lead a global team overseeing pharmacovigilance process, qualification, and training within a GxP framework.
Responsibilities include developing end-to-end processes, ensuring compliance, and collaborating with R&D and medical safety partners.
Leading strategic process improvements, managing staff development, and representing the PVQM function to senior leadership are key.
Requires a Master's degree, 12+ years of experience in pharma/regulatory compliance, and strong leadership skills.
Must possess excellent communication, regulatory knowledge, and proficiency in digital tools. Preferred skills include process mapping.
This role offers a hybrid work environment with a pay range of $150,000–$258,750, including benefits and incentives.