12.06.24 | 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
Später ansehen12.06.24 | Vollzeit | Le Locle | Randstad Schweiz AGSystems, analyze and report results) - Manage site bioburden and dose audit programs - Carry out microbiology/HPLC laboratory investigation - Review and approve laboratory documents & sterilization certificates - Support equipment qualification affecting cleanliness/sterilization - Review and assess
Später ansehen14.05.24 | Vollzeit | Neuchâtel | Randstad Schweiz AGHe/she must ensure the quality of information reported within the various systems and documentation with respect to current guidelines, compliance and regulatory requirements. General information - Start date asap - Planned duration of employment 8 months - Workplace Neuchatel - Workload 100
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