29.04.24 | Vollzeit | Neuchâtel | LHHDiscipline - Expert knowledge and understanding of stability ICH Guidelines (Q1A, Q5C) and associated policies, directives and guidance documents. A thorough knowledge of cGMP regulations as referenced in The Code of Federal Regulations (21CFR) and their specific application to stability programs
Später ansehen25.03.24 | Vollzeit | Neuchâtel | LHHDiscipline - Expert knowledge and understanding of stability ICH Guidelines (Q1A, Q5C) and associated policies, directives and guidance documents. A thorough knowledge of cGMP regulations as referenced in The Code of Federal Regulations (21CFR) and their specific application to stability programs
Später ansehen25.04.24 | Vollzeit | Neuchâtel | Michael Page InternationalJob Description - Develop and optimize HR processes. - Conduct reviews and updates of company regulations and internal documents. - Enhance workplace tools, such as competency management systems. - Lead the implementation of new HR software solutions. The Successful Applicant - Has at least 10 years
Später ansehen25.04.24 | Vollzeit | Neuchâtel | Michael Page InternationalPresence Stellenbeschreibung - Develop and optimize HR processes. - Conduct reviews and updates of company regulations and internal documents. - Enhance workplace tools, such as competency management systems. - Lead the implementation of new HR software solutions. Anforderungsprofil - Has at least 10 years
Später ansehen28.03.24 | Vollzeit | Le Locle | Randstad Schweiz AGAre in place to fix the issue in a - compliant manner. - Manages or participates to quality projects CAPA - Act as CAPA Process Owner - Ensure CAPAs are managed in compliance with internal procedures as well as applicable standards - Follow up CAPA process and ensure CAPA are handled and documented adequately
Später ansehen28.03.24 | 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
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