Stellenangebote für It Quality Manager Pharma Jobs in der Schweiz

03.04.24 | Vollzeit | Visp | Randstad Schweiz AGFor Lonza SGIE AG in Visp we are looking für a CQV Lead 100% (f/m/d). The CQV Lead Upstream is primarily responsible for the preparation and the execution of the CQV activities relating to Upstream Process Equipment. Accountabilities - Self-manage CQ development and execution activities

25.03.24 | Vollzeit | Bern | Galenica AGPower BI Developer (w/m) 80-100% What you can do - Develop, maintain and manage reporting, dashboards and other BI solutions using Power BI - Understand and translate business needs and requirements into robust and scalable technical solutions - Design and develop the appropriate data models

26.03.24 | Vollzeit | Bern | Randstad Schweiz AGFor our client, a pharmaceutical company based in Bern, we are seeking a highly skilled Sr Engineer Projects Automation. The aim of this role is to manage Engineering Projects to support the development and manufacture of Pharmaceuticals in a regulated environment and maximize the benefit

15.03.24 | Vollzeit | Kaiseraugst | Randstad Schweiz AGDo you possess extensive experience as SAP Master Data Analyst? Are you someone who is motivated by challenges? Do you have a passion for analyzing data and understanding it? We are currently seeking a SAP Master Data Analyst for a leading pharmaceutical and diagnostic company in Switzerland. Tasks

04.12.23 | Vollzeit | Hays AGWith IT, Maintenance Automation and Quality Operations groups o Contribute to ensure that changes introduced in the organization of systems, procedures, processes and formulas are managed so that all aspects of the equipment or computerized systems commissioning, and qualification process are assessed and resolved

05.11.19 | Vollzeit | Schlieren | headcount AGTo become a permanent position. The main tasks include mostly organizing projects and leading the project managers, liaising with KOLs, protocol development, CRO selection and management. \ Accountable for the planning, implementation and execution of the clinical trial according to ICH, GCP and other