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26 postes trouvés
    • Viège
    • Negotiable
    • Posté 2 jours .

    Description: Als Mitglied unseres QC Bioanalytics Microbial Teams beschäftigen Sie sich mit der Freigabeanalytik von biopharmazeutischen Wirkstoffen zur klinischen und kommerziellen Anwendung unter Einhaltung der GMP- und Sicherheitsrichtlinien. Ihre Aufgaben: - Planung und Mitverantwortung bei d...

    • Viège
    • Negotiable
    • Posté 2 jours .

    Description: Responsibilities and activities are focused on scientific and regulatory expertise within the field of process validation. Key responsibilities: Develop the strategy for the process-specific validations in biotechnology processes with focus on Mammalian Large Scale (ORCA). Issue proc...

    • Viège
    • Negotiable
    • Posté 3 jours .

    Description Summary: The Commissioning Qualification Validation engineer carries out a variety of tasks related to the validation of equipment and facilities. The scope of activities includes the coordination on the installation of equipment, drafting the IQ/OQ/PQ protocols, execution of the IQ/O...

    • Canton du Valais
    • Negotiable
    • Posté 3 jours .

    Key Duties of Project Coordinator: - Gathers all project information: schedules, data requests, assignments, tasks, and project meetings. - Works with project team to understand and assist with tracking all work, task and project assignments. - Working with Project Manager, assist in developing a...

    • Bâle
    • Negotiable
    • Posté 3 jours .

    Full Stack Developer Experis is the global leader in professional resourcing and project-based workforce solutions. On behalf of our Pharmaceutical company in Basel we are looking for a Full Stack Developer with proficiency in both Python front-end and back-end development, with a focus on expand...

    • Viège
    • Negotiable
    • Posté 4 jours .

    Description: Für den Standort Visp suchen wir aktuell eine/n Schichtmitarbeiter/in in der QC-FCC (API). Ihre Aufgaben: * die Durchführung und Freigabe von In-Process Kontrollen (UV, GC, Titrationen, pH, HPLC usw.) unter Einhaltung der cGMP Richtlinien * Instandhaltung bestehender Infrastrukturen ...

    • Viège
    • Negotiable
    • Posté 8 jours .

    Description: Technical role within Manufacturing operations area in charge of managing and/or supporting different gmp relevant type of GMP deliverables for the organization, including, Deviation investigation, CAPAs and CRs. Support the departments of the area to ensure appropriate level of audi...

    • Viège
    • Negotiable
    • Posté 9 jours .

    Description: * Acting a support for daily, short notice admin tasks such as ad hoc meetings, distribution list maintenance, act as a share point access approver, support on HR / recruiting tasks, hotel and travel booking for key stake holders, replying to Nexus Admin Inbox requests, visa requests...

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