Manager, GD Quality Management

At Johnson & Johnson, the Manager, Process & Personnel Qualification Management will be part of the R&D Quality Team, focusing on driving compliance and quality excellence in the pharmaceutical industry. The company is dedicated to healthcare innovation, aiming to prevent, treat, and cure complex diseases through innovative medicine and MedTech solutions. This role is based in Zug, Switzerland. The main responsibilities include leading process and training-related projects, such as process development, mapping, and training delivery. The manager will act as a quality partner for Global Development, fostering collaboration between business partners, quality groups, and governance. Ensuring the GxP Quality Framework adapts to both business and regulatory changes is a key part of the role. Managing tasks, timelines, and deliverables, as well as addressing issues and risks, will be crucial for successful project outcomes. Additionally, the manager will support the implementation of the digital transformation roadmap, driving the evolution towards a data-centric content and 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. Proficiency in both oral and written English communication, with the ability to articulate complex ideas clearly, is essential. Understanding of global (pre)clinical safety and pharmacovigilance compliance regulations, along with experience in the life sciences industry's regulatory framework, is also necessary. Demonstrated expertise in managing intricate projects and fostering collaboration among diverse teams and departments is crucial. Nice-to-have skills include experience in Business Process Management (BPM), Business Requirements Analysis, and Coaching. Familiarity with Compliance Management, Cross-Functional Collaboration, and Data Savvy is also beneficial. The role offers the opportunity to work in an inclusive environment that values diversity and provides a supportive work atmosphere. What the role asks for: - Bachelor's degree in Science or Business - 5 years of experience in a medium to large-scale matrix organization - 5 years of experience in pharmaceutical/device compliance - Proficiency in both oral and written English - Understanding of global (pre)clinical safety and pharmacovigilance compliance regulations - Experience in the life sciences industry's regulatory framework - Demonstrated expertise in managing intricate projects - Keen attention to detail and robust analytical thinking abilities