Die Bachem-Gruppe investiert in einen neuen geplanten Standort im Sisslerfeld (BSF) in der Nordwestschweiz. Dieser Schritt ist Teil der langfristigen Strategie, die Produktionskapazitäten bis zum Ende des Jahrzehnts auszubauen. Der neue Produktionsstandort wird eine zentrale Rolle
Die Bachem-Gruppe investiert in einen neuen geplanten Standort im Sisslerfeld in der Nordwestschweiz. Dieser Schritt ist Teil der langfristigen Strategie, die Produktionskapazitäten bis zum Ende des Jahrzehnts auszubauen. Der neue Produktionsstandort wird eine zentrale Rolle bei
Mission The Clinical Development Quality Manager (CDQM) is responsible for ensuring quality oversight across clinical development activities and supporting the maintenance of GCP compliance. This role supports stakeholders in vendor qualification, study risk management, quality oversight, team training
Die Bachem-Gruppe investiert in einen neuen geplanten Standort im Sisslerfeld in der Nordwestschweiz. Dieser Schritt ist Teil der langfristigen Strategie, die Produktionskapazitäten bis zum Ende des Jahrzehnts auszubauen. Der neue Produktionsstandort wird eine zentrale Rolle bei
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By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms
At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.Through our
Salary Range:CHF76,300.00 - CHF141,700.00 Job Description SummaryLocation: Basel, Switzerland #onsite Role Purpose: We are seeking a highly motivated Expert Analytical Scientist with experience in Oligonucleotides analytics to join our Analytical Research & Development (ARD) team. ARD is
Salary Range:CHF93,800.00 - CHF174,200.00 Job Description SummaryLocation: Basel, Switzerland #onsite Role Purpose: We are seeking a highly motivated Senior Expert Analytical Scientist with experience in Oligonucleotides analytics to join our Analytical Research & Development (ARD) team. ARD
Company Description Eurofins Scientific is an international life sciences company that offers customers from various industries a unique range of analytical services to make life and our environment safer, healthier and more sustainable. From the food
Position Summary: The EU CTR Submission Lead is responsible for leading and overseeing the full lifecycle of regulatory submissions for clinical trials conducted under the EU Clinical Trial Regulation (EU CTR 536/2014) via the Clinical Trials
The actual location of this job is in Stein, AG, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed. Join Lonza AG as a (Senior) QA Expert Compliance, partnering with senior stakeholders
Die Bachem-Gruppe investiert in einen neuen geplanten Standort im Sisslerfeld (BSF) in der Nordwestschweiz. Dieser Schritt ist Teil der langfristigen Strategie, die Produktionskapazitäten bis zum Ende des Jahrzehnts auszubauen. Der neue Produktionsstandort wird eine zentrale Rolle
Ever wondered how your skills and unique background could impact the world of tomorrow? Join our EHS Office team and bring your passion and talent to work. Product Environmental Compliance Manager (80-100%) Männedorf, Zürich Your contribution
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,
Microcaps is an ETH Zurich spin-off founded in March 2019. Our unique technology allows us to produce highly precise and innovative microcapsules that empower materials to unlock new capabilities; all tailored to various markets from cosmetics
Shape the future of bioanalysis for innovative medicines Celerion is a leading global contract research organization (CRO) specializing in early clinical research and bioanalytical services. For more than 40 years, we have partnered with pharmaceutical and
Are you passionate about patient safety and ensuring that medicines are monitored to the highest standards? As a Drug Safety Case Manager, you will play a critical role in safeguarding patients by ensuring accurate and timely
Work Your Magic with us! Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich
Location: The actual location of this job is in Visp, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed. The role: The Senior QA Specialist (f/m/d) for QA Projects specifies quality requirements