Leading the strategic build-out and lifecycle management of Quality Management System documentation, the remote Project Manager, Quality Management Systems & Documentation will manage controlled documentation initiatives, coordinate cross-functional stakeholders, and ensure compliance with regulatory requirements in a 6-12 month contract role. Key responsibilities: Develop and maintain the enterprise SOP Development Master Plan and manage the end-to-end lifecycle of controlled procedures Coordinate cross-functional meetings to design, develop, and implement regulated processes while tracking documentation-related actions and milestones Ensure all documentation activities comply with applicable GxP regulations and company objectives, providing routine reports to the Sr. Director of Quality Required qualifications: Bachelor's degree in Life Sciences, Engineering, Pharmaceutical Sciences, Quality, Business, or Project Management 8+ years of experience in pharmaceutical, biotechnology, or medical device industries 3+ years of experience managing cross-functional projects Experience with controlled documentation and supporting GxP Quality Systems Experience implementing or managing electronic Quality Management Systems (eQMS)
