We are seeking a highly skilled and experienced QC Support Investigation Expert to join our Quality Control team. The ideal candidate will have a strong engineering background and extensive experience in the pharmaceutical or biotech industry. The primary responsibility of the QC Support Investigation Expert will be to lead and support investigations related to quality control issues, deviations, and non-conformances in our manufacturing processes.Key Resp
We are seeking a highly skilled and experienced QC Support Investigation Expert to join our Quality Control team. The ideal candidate will have a strong engineering background and extensive experience in the pharmaceutical or biotech industry. The primary responsibility of the QC Support Investigation Expert will be to lead and support investigations related to quality control issues, deviations, and non-conformances in our manufacturing processes.Key Resp
For our client, an international company based in Solothurn, we are looking for a Associate II Quality Control.The Quality Associate assures that all operations meet or exceed cGMP regulations. The position needs reactive support of discrepancy identification. This position will support quality key metrics and analysis. This role is expected to be cross-functional between all parts of the quality line organization (QC, Corporate Quality and QA) as well as
For our client, an international company based in Solothurn, we are looking for a Associate II Quality Control.The Quality Associate assures that all operations meet or exceed cGMP regulations. The position needs reactive support of discrepancy identification. This position will support quality key metrics and analysis. This role is expected to be cross-functional between all parts of the quality line organization (QC, Corporate Quality and QA) as well as
For our client, an international company in Zürich, we are looking for a Quality Manager.General Information: Start date: ASAP/30.09.2024End date: 31.03.2026Extension: to be discussedWorkplace: ZürichHome office: possible, hybrid roleWorkload: 100%Responsibilities: Drive and support analytical method life cycle management (LCM) strategy for in-process, release and stability testing of commercial productsLeads multisite assay transfers via providing assay t
For our client, an international company in Zürich, we are looking for a Quality Manager.General Information: Start date: ASAP/30.09.2024End date: 31.03.2026Extension: to be discussedWorkplace: ZürichHome office: possible, hybrid roleWorkload: 100%Responsibilities: Drive and support analytical method life cycle management (LCM) strategy for in-process, release and stability testing of commercial productsLeads multisite assay transfers via providing assay t
For our client, an international biotech company based in Baar, we are looking for a Regulatory Affairs Senior Manager to join the Biosimilars Business Unit. The person will be responsible for leading regulatory affairs activities for assigned projects and programs and for leading affiliate RA to identify and complete national regulatory requirements for assigned projects and programs, to support commercialisation.General Information: Start date: ASAP / 02
For our client, an international biotech company based in Baar, we are looking for a Regulatory Affairs Senior Manager to join the Biosimilars Business Unit. The person will be responsible for leading regulatory affairs activities for assigned projects and programs and for leading affiliate RA to identify and complete national regulatory requirements for assigned projects and programs, to support commercialisation.General Information: Start date: ASAP / 02
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