About this role
- 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 supervision - Confident in collaborating with cross-functional stakeholders, including R&D, QC, Operations, and international Regulatory Affairs teams - Strong organizational, communication, and stakeholder management skills - Ability to prioritize, solve problems effectively, and deliver results in a global regulatory environment About Hays: With over 15 years of experience in the pharmaceutical and chemical industry as well as in biotechnology and medical engineering, we know the key contacts at companies that are recruiting for challenging jobs with real potential. The current high demand for staff has opened up exciting opportunities for dedicated experts who want to develop professionally and to further their careers. As recruitment specialists with an international network of contacts, we can offer you decisive advantages - completely free of charge. Register with us and reap the benefits of interesting job offers that match your skills and experience.