Batch Record Reviewer (m/f/d)
Firmenname für PREMIUM-Mitglieder sichtbar
- Juni 2024
- nicht angegeben
- CH-Wallis
- auf Anfrage
- 27.05.2024
- 763907/1-en
Projekt Insights
Projektbeschreibung
Ihre Aufgaben:
• Independent review of operational paper-based and electronic manufacturing records on schedule
• Checking whether the materials used were approved at the time of production
• Carrying out the audit trail reviews
• Checking whether required Filter Integrity Tests (FIT) are available and have been successfully completed
• Check whether trends, parameters and CPP are within the given limits
• Checking the LIMS labels for correct labeling in the manufacturing protocols
• Creating and editing CAPAs in the Trackwise system
• Collaboration in continuous improvement processes
• Participation in cross-departmental meetings (QA, BPEs)
• Implementation of logbook reviews
Ihre Qualifikationen:
• English mandatory / German is advantageous
• Completed vocational training required
• Accurate working and documentation skills required
• Execution of work with high safety and quality awareness required
• Strong team spirit required
• GMP experience an advantage
• Bachelor's degree (science, engineering) in chemistry, biology or similar is an advantage
Ihre Vorteile:
• A very renowned company
• A highly motivated team and an open way of communication
Projektdauer: 7 MM
Sie sind Freiberufler? Dann freuen wir uns auf Ihre Bewerbung!
• Independent review of operational paper-based and electronic manufacturing records on schedule
• Checking whether the materials used were approved at the time of production
• Carrying out the audit trail reviews
• Checking whether required Filter Integrity Tests (FIT) are available and have been successfully completed
• Check whether trends, parameters and CPP are within the given limits
• Checking the LIMS labels for correct labeling in the manufacturing protocols
• Creating and editing CAPAs in the Trackwise system
• Collaboration in continuous improvement processes
• Participation in cross-departmental meetings (QA, BPEs)
• Implementation of logbook reviews
Ihre Qualifikationen:
• English mandatory / German is advantageous
• Completed vocational training required
• Accurate working and documentation skills required
• Execution of work with high safety and quality awareness required
• Strong team spirit required
• GMP experience an advantage
• Bachelor's degree (science, engineering) in chemistry, biology or similar is an advantage
Ihre Vorteile:
• A very renowned company
• A highly motivated team and an open way of communication
Projektdauer: 7 MM
Sie sind Freiberufler? Dann freuen wir uns auf Ihre Bewerbung!
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