Descripción
- Roche Diagnostics GmbH in Penzberg is one of the largest biotechnology centers in Europe, offering not only an outstanding market position but also an exciting and innovative working environment Your Benefits: - 30 days leave per year - A highly motivated team and an open way of communication - A very renowned company - Support throughout the entire application process Your Duties: - Deep understanding of global healthcare regulatory frameworks and compliance requirements - Ability to develop and execute regulatory strategies for complex products and submissions - Strong expertise in managing product registration dossiers and regulatory documentation - Excellent stakeholder management and relationship-building skills across internal and external partners - Ability to influence, communicate effectively and drive alignment without direct authority - Independent decision-making combined with sound judgment in complex situations - Strong innovation mindset with a focus on continuous improvement and digitalization - Advanced problem-solving skills with the ability to identify and implement effective solutions - Agile mindset with a willingness to embrace change, simplify processes and increase productivity - Strong collaboration skills with the ability to bring teams together and achieve common goals Your Qualifications: - Bachelor's or Master's degree in Life Sciences, Data Science, or a related field, alternatively equivalent technical or laboratory qualification - Experience in Regulatory Affairs, R&D, Quality, Operations, Clinical Affairs, or a related healthcare environment - Experience in healthcare regulatory affairs and regulatory compliance activities - Ability to manage complex projects and navigate challenging regulatory requirements independently - Strong understanding of regulatory submission processes and product registration activities - Fluent English communication skills, both written and spoken - Self-driven and able to work independently with minimal