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CSL Vifor is a global partner of choice for pharmaceuticals and innovative, leading therapies in iron deficiency, dialysis and nephrology & rare disease. We specialize in strategic global partnering, in-licensing and developing, manufacturing and marketing pharmaceutical products for precision healthcare, aiming to help patients around the world lead better, healthier lives. We are currently looking for a QA Manufacturing Science Manager for our Parenteral Products to join our team in St. Gallen. In this exciting position, you will be in charge of the Quality oversight of GMP data trending... more ->
Responsibilities: The Pharmacovigilance & Regulatory Quality Assurance (PVRQA) Lead/PV Auditor is responsible for leading and coordinating the Global PVRQA activities in the respective region (Americas, Asia-Pacific (APAC), European Economic Area (EEA), ECI) under the general direction of the PVRQA Regional Head, to ensure that CSL's (CSL Behring/CSL Seqirus/CSL Vifor) entire Pharmacovigilance (PV) System is in compliance with applicable pharmacovigilance regulations and requirements, GVP, ICH GCP guidelines, respective GxP guidelines, international standards, relevant regulatory requirements... more ->
Oracle Database Administrator Are you an experienced Oracle Database Administrator having strong skills with Oracle databases? As well as having strong experience with PowerShell, Windows and Linux. Then this could be your chance. You will be responsible for monitoring database performance, implementing changes, and applying new patches and versions when required. At the same time, you will be ensuring all hardware and software are updated as well as monitoring the performance of hardware and software. And configuring Servers and databases while also preserving data integrity. You will be... more ->