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Dormont Manufacturing Co in Zaventem, Belgium, seeks to enhance global health through effective system validation in clinical trials. Join a dedicated team focused on project timelines and regulatory inspections, ensuring quality and accuracy in deliverables.
The ideal candidate has a Bachelor's degree, strong MS Office skills, and a solid understanding of clinical trial processes. With responsibilities including instrument system validation and network support, this is an opportunity to make meaningful contributions in a dynamic environment.
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At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future.
This role is part of a small global team focused on validating the lab instrumentation in accordance with the European Medicines Agency (EMA) guidelines. This role will work on system development lifecycle deliverables, work on project timelines, participate in client and regulatory inspections, and work closely with various departments and vendors to ensure effective communication, accuracy, and support throughout the project lifecycle.