[DOT379] - QUALITY DOCUMENTATION SPECIALIST

Documentation lifecycle manager - responsible for the end-to-end management of documentation lifecycle in a regulated environment. about the role as a key member of the global m&s; services team, you will play a vital role in delivering and supporting high-quality documents and processes that meet regulatory requirements. your primary focus will be on executing administration and governance-related tasks, including format improvement, process optimization, and stakeholder management. you will also be responsible for managing and monitoring the documentation update process, ensuring timely completion of periodic reviews, and participating in local document governance meetings. additionally, you will coordinate gap assessment processes, monitor progress, and report on key performance indicators (kpis). with strong analytical skills and attention to detail, you will provide expert responses to simple questions, extract data, and generate reports as needed. proficiency in quality dms and edms systems, as well as microsoft office suite, is essential for this role. requirements - minimum 3 years of experience in documentation lifecycle management in the pharmaceutical industry or gxp regulated environment. - strong problem-solving skills, attention to detail, and good organizational skills. - ability to work collaboratively with cross-functional teams in a flexible and proactive manner. - excellent english communication and writing skills; proficiency in spanish, portuguese, or french is an asset. - bachelor's or master's degree in life sciences, engineering, or related...