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Clario, part of Thermo Fisher Scientific, is seeking a Manager, R&D Software Quality to lead a team of manual and automated quality engineers. You will define test strategies, drive testing across multiple levels, and collaborate with R&D, Product, and Project Management to ensure on-time delivery in a regulated environment.
You will guide test planning, execution, and reporting, while advancing quality processes and automation practices in an Agile setting.
Manager, R&D Software Quality managing test automation teams working on products based on micro service based architecture
Join Clario, part of Thermo Fisher Scientific, as Manager, R&D Software Quality and play a critical leadership role in ensuring the quality, reliability, and compliance of our software solutions that support clinical research globally. You will lead a high‑performing Software Quality Engineering team and partner closely with R&D, Product, and Project Management to deliver high‑quality software in a fast‑paced, Agile environment.
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. Clario Privacy Policy Clario is a leading provider of endpoint data solutions to the clinical trials industry, generating high‑quality clinical evidence for life sciences companies. We offer comprehensive evidence generation solutions that combine medical imaging, eCOA, precision motion, cardiac solutions and respiratory endpoints. For more than 50 years, Clario has delivered deep scientific expertise and broad endpoint technologies to help transform lives around the world. Our endpoint data solutions have supported over 30,000 clinical trials in more than 100 countries. Our global team of science, technology, and operational experts have supported over 70% of all FDA drug approvals since 2015.