06.05.24 | Vollzeit | Neuchâtel | LHHAuthor stability sections of CTD dossiers for post-approval filings, annual reports, product renewals, Annual Product Stability Reviews, and stability related responses to health authority inquiries. - Serve as stability representative for OOT/OOS investigations, Market Action Fact Finding, and other
Später ansehen25.03.24 | Vollzeit | Neuchâtel | LHHAuthor stability sections of CTD dossiers for post-approval filings, annual reports, product renewals, Annual Product Stability Reviews, and stability related responses to health authority inquiries. - Serve as stability representative for OOT/OOS investigations, Market Action Fact Finding, and other
Später ansehen06.03.24 | Vollzeit | Bern | Randstad Schweiz AGBy regulatory authorities - Validation Master plans are up to date and established for all ongoing projects Essential duties - Assess and produce the CSV package(s) on an assigned project. Taking accountability for the work to be produced by yourself and other colleagues that are under the assigned packages
Später ansehen04.12.23 | Vollzeit | Hays AGRequirements and requirements set by regulatory authorities o Ensure that Validation Master plans are up to date and established for all ongoing projects o Assess and produce the CSV package(s) on an assigned project. Taking accountability for the work to be produced o Plan, coordinate and execute all phases
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