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On behalf of our client, a leading global pharmaceutical company, we are looking for a QA engineering/Validation Expert to join the Quality engineering department. Start Date: As soon as possible Location: Neuchatel Work type: Minimum 3 days on site per week. Workload: 100% Duration: 8 months Extension: Possible Your mission: - Review deviations in the framework of engineering events within quality systems (ie Trackwise) to verify acceptability and adherence to standard procedures and regulatory requirements. This includes conducting or approving the relevant investigations, impact... 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 ->