Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the fastest-growing SaaS companies in history, we surpassed $3B in revenue in our last
Revolution Medicines is a late-stage clinical oncology company developing novel targeted therapies for patients with RAS-addicted cancers. The company’s R&D pipeline comprises RAS(ON) inhibitors designed to suppress diverse oncogenic variants of RAS proteins. The company’s RAS(ON)
To drive our continuous organic growth, we are constantly looking for highly qualified professionals. To strengthen our team in Global IT, we are looking for a dedicated IT Cloud Engineer (a), 80-100% Your tasks: Manage and
Job Description We are looking for an experienced, quality-focused professional to join our team in Technical Support Packaging. In this role, you will independently manage and support quality-related and technical activities in a GMP-regulated environment, including
Department:607000 Regulatory - TTSG Location:Rapperswil-Jona (SG), Switzerland Be a part of a global team that is inspired to make a difference in the lives of people living with rare disease. At Travere Therapeutics, we recognize that
Revolution Medicines is a late-stage clinical oncology company developing novel targeted therapies for patients with RAS-addicted cancers. The company’s R&D pipeline comprises RAS(ON) inhibitors designed to suppress diverse oncogenic variants of RAS proteins. The company’s RAS(ON)
Revolution Medicines is a late-stage clinical oncology company developing novel targeted therapies for patients with RAS-addicted cancers. The company’s R&D pipeline comprises RAS(ON) inhibitors designed to suppress diverse oncogenic variants of RAS proteins. The company’s RAS(ON)
Revolution Medicines is seeking an Associate Director, Regulatory Operations, Europe to lead operational planning and execution of regulatory submissions across the EU, EEA, UK and Switzerland. You will partner with Regulatory Affairs, CMC, clinical and quality
Founded in 1921 and headquartered in Mendrisio (Switzerland), Sinteticas mission is to continuously strive to improve therapies by enhancing its products formulations and usability for the benefit of clinicians and patients. We do so in close
BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our
Global Quality Manager (m/f/d) – Quality Assurance / GMP / GDP / Pharma / English Project: For our customer a big pharmaceutical company in Basel we are looking for a highly qualified Global Quality Manager (m/f/d)