2 jobs found in luterbach, solothurn

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    • luterbach, solothurn
    • contract
    For one of our clients in Solothurn we are looking for Quality Assurance Associate for a 4 months project: Responsibilities: Responsible for Quality oversight to review and approval of validation and engineering life cycle documents (URS, FS, RTM, RA, DS, configuration spec, drawings etc), test protocols, CAPAs, deviations, change controls, work orders and any technical documentation in the scope of Facilities, utilities, equipment and Execution System (global and local computerized systems) to enable start up, commissioning and qualification of new Large Scale Manufacturing facility. Furthermore advice the project groups as appropriate and be an active member of the groups where the quality input is needed. Additional Info: This position requires co-operation with people at every level of the organization and from multiple functions, including engineering, automation, validation, Manufacturing personnel, SME’s on equipment and knowledge of biotechnology API production. Good communication skills in English, verbally and written. Technically orientated role including experience of the validation of laboratory, production equipment and knowledge of production methodology involved in biopharmaceutical drug substance production. Self-driven and take ownership and responsibility for own assignments. Value teamwork at all levels, performs work with an open-mind and ability to value input from colleagues and peers. Able to drive discussion to solve problems with cross functional teams. Be confident in making technical decisions. In addition must be able to prioritize tasks, be flexible and able to keep many activities running at a time.
    For one of our clients in Solothurn we are looking for Quality Assurance Associate for a 4 months project: Responsibilities: Responsible for Quality oversight to review and approval of validation and engineering life cycle documents (URS, FS, RTM, RA, DS, configuration spec, drawings etc), test protocols, CAPAs, deviations, change controls, work orders and any technical documentation in the scope of Facilities, utilities, equipment and Execution System (global and local computerized systems) to enable start up, commissioning and qualification of new Large Scale Manufacturing facility. Furthermore advice the project groups as appropriate and be an active member of the groups where the quality input is needed. Additional Info: This position requires co-operation with people at every level of the organization and from multiple functions, including engineering, automation, validation, Manufacturing personnel, SME’s on equipment and knowledge of biotechnology API production. Good communication skills in English, verbally and written. Technically orientated role including experience of the validation of laboratory, production equipment and knowledge of production methodology involved in biopharmaceutical drug substance production. Self-driven and take ownership and responsibility for own assignments. Value teamwork at all levels, performs work with an open-mind and ability to value input from colleagues and peers. Able to drive discussion to solve problems with cross functional teams. Be confident in making technical decisions. In addition must be able to prioritize tasks, be flexible and able to keep many activities running at a time.
    • luterbach, solothurn
    • contract
    For our biotech client in Solothurn we are looking for aManufacturing Associate IIIContract: until 31.03.2022 Tasks:Executes manufacturing processing steps and/or manufacturing support activities, monitoring the process against the recipe & MFG documentationPerform troubleshooting/investigation of equipment and process issuesRevises documents as instructed, Capable of equipment and/or process changesActively participates in training activities, managing their individual training plan.  Trains other associates as required.Executes validation protocolsCapable of leading shift when supervisor is absent, and actively leads or participates in shift exchanges.  Coordinates activities and daily schedules with cross-functional areas.And other job duties that may be assigned from time to time.Qualifications:Relevant education from chemical industry, food industry, pharmaceutical or biotech industry.basic knowledge of biopharmaceutical technology and processessolid understanding of the requirements within correct and timely documentation within a cGMP environmentknowledge in all operational and regulatory procedures of manufacturing department
    For our biotech client in Solothurn we are looking for aManufacturing Associate IIIContract: until 31.03.2022 Tasks:Executes manufacturing processing steps and/or manufacturing support activities, monitoring the process against the recipe & MFG documentationPerform troubleshooting/investigation of equipment and process issuesRevises documents as instructed, Capable of equipment and/or process changesActively participates in training activities, managing their individual training plan.  Trains other associates as required.Executes validation protocolsCapable of leading shift when supervisor is absent, and actively leads or participates in shift exchanges.  Coordinates activities and daily schedules with cross-functional areas.And other job duties that may be assigned from time to time.Qualifications:Relevant education from chemical industry, food industry, pharmaceutical or biotech industry.basic knowledge of biopharmaceutical technology and processessolid understanding of the requirements within correct and timely documentation within a cGMP environmentknowledge in all operational and regulatory procedures of manufacturing department

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