Job Opportunities API

Join Clario, part of Thermo Fisher Scientific, as Director, Regulatory Affairs (f/m/d) and play a critical role in ensuring that innovative clinical trial technologies meet global regulatory standards - helping bring life-changing therapies to patients faster. In this role, you will shape regulatory strategy, guide cross-functional teams, and ensure compliance across global markets, making a meaningful impact on patient safety and product quality. What we offer • Competitive compensation. • Flexible working hours and working time accounts to support the work-life balance. • Hybrid work model, allowing for 1-2 days of remote work. • Support your professional development through internal and external training and certification programs. • Attractive benefits (security, flexibility, support and well-being). • Engaging employee programs. What you'll be doing • Lead global regulatory activities to ensure compliance with FDA 21 CFR 820, ISO 13485, and international medical and non-medical device regulations • Define and implement regulatory strategies across the full product lifecycle, from development to post-market • Partner with Product Management, Logistics, and Engineering teams to ensure compliant product development and global market access • Establish and optimize global processes for trade compliance, import/export, and supply chain regulatory requirements • Guide and mentor a team of hardware and software development engineers, providing regulatory expertise across projects such as respiratory, imaging, and cardiac safety solutions • Assess regulatory impact of changes to design, materials, labeling, software, and suppliers • Support regulatory submissions, including FDA 510(k) filings and international product registrations • Review and approve product labeling, technical documentation, and marketing materials to ensure regulatory alignment • Participate in internal, external, and vendor audits and contribute to corrective and preventive action initiatives • Act as Person Responsible for Regulatory Compliance (PRRC) under MDR requirements • Oversee the development and maintenance of SOPs and work instructions aligned with global standards • Support post-market surveillance, vigilance reporting, and continuous improvement activities What we look for • Master’s degree in Engineering, Life Sciences, or a related technical field • 6+ years of experience in the medical device industry • 4+ years of experience in Regulatory Affairs within medical devices or pharmaceutical products • 3+ years of proven leadership experience managing or guiding teams • Strong knowledge of FDA regulations, ISO standards, and global medical device requirements (including 510(k) submissions and MDR) • Experience interacting with regulatory authorities and supporting audits and inspections • Understanding of clinical trial environments and GCP is highly desirable • Excellent analytical, organizational, and communication skills • Fluency in English and German • Detail-oriented with strong problem-solving capabilities and the ability to manage complex regulatory challenges At Clario, part of Thermo Fisher Scientific, our purpose is to transform lives by unlocking better evidence. It’s a cause that unites and inspires us. It’s why we come to work—and how we empower our people to make a positive impact every day. Whether you're advancing clinical science, building innovative technology, or supporting our global teams, your work helps bring life-changing therapies to patients faster.