17.06.24 | Vollzeit | Bern | Randstad Schweiz AGAre required - Being responsible for completion (i.e., execution and documentation) of different analytical tests according to internal (TMDs) and/or external (e.g., EP, USP, ISO) requirements. Analytical tests encompass EP/USP ion ID tests, FTIR, TLC, Appearance of solution, pH, Osmolality, Density
Später ansehen17.06.24 | Vollzeit | Visp | Randstad Schweiz AGProcess - Sourcing and management of contingent workers for CAPEX projects and supporting functions - Manage candidate life cycle (from application to onboarding) - Perform candidate offers including vendor rate negotiation - Documentation repository management in alignment with corporate policies
Später ansehen17.06.24 | Vollzeit | Bern | Randstad Schweiz AGMain Responsibilities - Perform Technology Transfer of a new process into GMP Manufacturing (writing of Process relevant documents like Process Description, MBR's (first draft), Work Instructions etc - Training of Operators on new - written documents - Writing of Reports (TechTransfer/Campaign
Später ansehen17.06.24 | Vollzeit | Lausanne | Randstad Schweiz AGDefinition, implementation, execution, and documentation - Install necessary software using your IT and programming skills - Supervision of team compliance with company software development procedures - Ideally, use Python for automated testing projects. - Understand basic C/C+ to help with team tasks. Your
Später ansehen17.06.24 | Vollzeit | Bern | Randstad Schweiz AGPerform Technology Transfer of a new process into GMP Manufacturing (writing of Process relevant documents like Process Description, MBR's (first draft), WorkInstructions etc - Training of Operators on new - written documents - Writing of Reports (TechTransfer/Campaign), Technical documents like Risk
Später ansehen17.06.24 | Vollzeit | Basel (Basel-Stadt) | Randstad Schweiz AGAnd conducting qualification and validation activities - Creating and reviewing qualification and validation documents - Producing SOPs and providing support in the creation of manufacturing specifications - Responsible for maintaining the qualified and validated status of rooms, infrastructure and equipment
Später ansehen14.06.24 | Vollzeit | Corsier-sur-Vevey | Randstad Schweiz AGSampling, aliquoting, utility sampling, HVAC, Gases, corrections of working papers, ) - Perform support activities (autoclave and part washer) - Carrying out the documentation related to your function (e.g. writing working instructions) - Supporting compliance activities (batch review, deviations
Später ansehen13.06.24 | Vollzeit | Basel (Basel-Stadt) | Randstad Schweiz AGExpert for GxP-related questions. - Manage Third-Party providers by updating agreements, conducting Quality Review Meetings, ensuring regulatory documentation, and reviewing stability data. - Review third-party Change Control, Deviations, CAPA, and Complaints using risk management principles
Später ansehen12.06.24 | Vollzeit | Schaffhausen | Randstad Schweiz AGZu den führenden Pharmaunternehmen der Schweiz und ist gleichzeitig ein strategischer Einführungs- und Wachstumsstandort. Als Quality Systems Documentation and Training Specialist sind Sie in einem vielseitigen Team für die Verwaltung von GMP-Dokumenten und -Schulungen am Standort Johnson&Johnson Schaffhausen
Später ansehen12.06.24 | Vollzeit | Le Locle | Randstad Schweiz AGRequirements - Ensures that quality activities for validation of new processes/ products are performed and documented according to procedures and within the defined timeline - Write protocols and reports for validation documentation (such as process validation, test method validation, validation plan
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