Darum lohnt es sich
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 work‑life balance Hybrid work model, allowing 1-2 days of remote work per week Support for professional development through internal and external training and certification programs Attractive benefits – security, flexibility, support, and well‑being Engaging employee programs Responsibilities 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 Overview 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.
