At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are,
Category Manager Packaging Location: Zurich, CH, 8005 At Barry Callebaut, we are on a journey to transform the cocoa and chocolate industry. As the world’s leading manufacturer of high-quality chocolate and cocoa products, our actions truly shape
Join Tether and Shape the Future of Digital Finance At Tether, we’re not just building products, we’re pioneering a global financial revolution. Our cutting-edge solutions empower businesses—from exchanges and wallets to payment processors and ATMs—to seamlessly
Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department.
Company kp is a globally recognised leader in the packaging and specialty film industry, renowned for its unwavering commitment to sustainability and innovation. The need to act on climate change has never been clearer so we incorporate
Senior Linux Platform Engineer: Linux Mastery / Debian / MedTech / Linux stack / Python / Shell / Cmake / Containers / Docker/ Kubernetes /English Project: For our customer a big pharmaceutical company in Rotkreuz, we
Position: Linux Software Engineer (SW/HW expert Debian/Python/go/Angular/C++) Location: Rotkreuz, Switzerland (Hybrid + onsite 2 days weekly) In-country candidates are considered only Type: Contract Duration: 12 Months + potential extensions Start: 30 October or ASAP thereafter Language:
Overview Regulatory Affairs Intern at Johnson & Johnson, Switzerland | Life Sciences Candidates Job Title: Regulatory Affairs Intern Requisition number: R- About the Company Johnson & Johnson is a global healthcare titan built on the belief
The Clinical Supplies Quality team is responsible for release of the packaged and labeled drugs for usage in clinical studies. The team is responsible from release of clinical and commercial drugs, incoming label stock and primary
For one of our clients, an international pharmaceutical company, we are seeking a Clinical Supplies Quality Specialist. General Information End Date: Home office: possible Working hours: Standard About the work The Clinical Supplies Quality team is