Manager, GD (Global Development) Quality Management

Johnson & Johnson is a global leader in healthcare innovation, dedicated to preventing, treating, and curing complex diseases. The company focuses on developing smarter, less invasive treatments and personalized solutions. The Manager, GD (Global Development) Quality Management role is part of the R&D Quality Team, driving compliance and quality excellence in the pharmaceutical industry. This position involves leading process improvement projects and supporting the digital transformation of traditional processes into a data-centric content and qualification management system. The main day-to-day responsibilities include leading process and training-related projects, such as process development, mapping, and training delivery. The role also involves promoting collaboration between business partners, quality groups, and governance, ensuring the GxP Quality Framework adapts to both business and regulatory changes. Managing tasks, timelines, and deliverables, as well as addressing issues and providing updates to management, are crucial for successful project outcomes. Additionally, the role supports the implementation of the digital transformation roadmap, driving the evolution towards a robust qualification management system. To excel in this role, candidates must have a Bachelor's degree in Science or Business, with a Master's degree being preferred. A minimum of 5 years of experience in a medium to large-scale matrix organization, with at least 5 years focused on pharmaceutical/device compliance, is required. Exceptional proficiency in both oral and written English communication, along with a strong understanding of global (pre)clinical safety and pharmacovigilance compliance regulations, is essential. Demonstrated expertise in managing intricate projects and fostering collaboration among diverse teams is also crucial. Nice-to-have skills include experience in process design and training design, as well as proficiency in Business Process Management (BPM), Business Requirements Analysis, and Compliance Management. The role is based in various locations, including Allschwil, Basel-Country, Switzerland, Beerse, Antwerp, Belgium, Breda, Netherlands, High Wycombe, Buckinghamshire, United Kingdom, Horsham, Pennsylvania, United States of America, and Titusville, New Jersey, United States of America. The team values diversity and inclusivity, providing an environment where each person is considered as an individual. The role offers opportunities for growth and development, with a focus on personal leadership and building relationships. What the role asks for: - Bachelor's degree in Science or Business - 5 years in a medium to large-scale matrix organization - 5 years focused on pharmaceutical/device compliance - Exceptional proficiency in both oral and written English - Understanding of global (pre)clinical safety and pharmacovigilance compliance regulations - Demonstrated expertise in managing intricate projects - Keen attention to detail and robust analytical thinking abilities - Established track record in personal leadership, building relationships, working autonomously, and cultivating an inclusive work atmosphere that values diversity