For one of our clients, an international pharmaceutical company, we are seeking a GMP Documentation Specialist.General Information:Start date: 26.10.2026End Date: 30.06.2027Workplace: Schachen, LuzernWorkload: 100%Working hours: StandardHome Office: primarily onsiteAbout the work:The GMP Documentation Specialist supports clinical biologics manufacturing by performing operational review of executed batch records and ensuring documentation supports ALCOA+ st
For one of our clients, an international pharmaceutical company, we are seeking a GMP Documentation Specialist.General Information:Start date: 26.10.2026End Date: 30.06.2027Workplace: Schachen, LuzernWorkload: 100%Working hours: StandardHome Office: primarily onsiteAbout the work:The GMP Documentation Specialist supports clinical biologics manufacturing by performing operational review of executed batch records and ensuring documentation supports ALCOA+ st
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