You will be a member of Pfizer’s dedicated and highly effective quality assurance team. contributing to the development and commercialization of transformative cancer therapies. The Document Control Supervisor is working supervisor role responsible for owning and managing GMP site Quality business processes supporting the lifecycle of documents as well as managing document control staff day-to-day duties. The position must be able to interact with staff at various management levels and make presentations to internal and external customers on specialized and highly technical aspects of the relevant program. Making decisions within the scope of the document management program; providing customer service and user support at the site by providing guidance and tools; developing metrics and assessing performance against them; authoring and collaborating on GMP controlled procedures within scope of responsibility; participating on cross-functional or external teams and continuous improvement activities. Working in a fast-paced environment where learning and personal development are actively encouraged, you will find the role both challenging and rewarding. What You Will Achieve In this role, you will:
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Job Type
Full-time
Career Level
Manager
Number of Employees
5,001-10,000 employees