Weigh and dispense associate Expert (m/f/d)
Firmenname für PREMIUM-Mitglieder sichtbar
- September 2024
- nicht angegeben
- CH-Solothurn
- auf Anfrage
- 18.09.2024
- 781346/1-en
Projekt Insights
Projektbeschreibung
Ihre Aufgaben:
• Executes Weigh and Dispense manufacturing operations and/or material management activities as per daily schedule
• Monitors the process against the recipe and MFG documentation
• Perform troubleshooting/investigation of equipment and process issues
• Revises documents as instructed, Capable of equipment and/or process changes
• Actively participates in training activities, managing their individual training plan
• Trains other associates as required
• Executes validation protocols
Ihre Qualifikationen:
• Education from chemical industry, food industry, pharmaceutical or biotech industry
• GMP knowledge desired
• Industry or process operator or technical craftsman.
• A basic knowledge of biopharmaceutical technology and processes
• Solid understanding of the requirements within correct and timely documentation within a cGMP environment
Ihre Vorteile:
• Good infrastructure
• Varied tasks in a renowned international biotech company
Projektdauer: 12 MM++
Sie sind Freiberufler? Dann freuen wir uns auf Ihre Bewerbung!
• Executes Weigh and Dispense manufacturing operations and/or material management activities as per daily schedule
• Monitors the process against the recipe and MFG documentation
• Perform troubleshooting/investigation of equipment and process issues
• Revises documents as instructed, Capable of equipment and/or process changes
• Actively participates in training activities, managing their individual training plan
• Trains other associates as required
• Executes validation protocols
Ihre Qualifikationen:
• Education from chemical industry, food industry, pharmaceutical or biotech industry
• GMP knowledge desired
• Industry or process operator or technical craftsman.
• A basic knowledge of biopharmaceutical technology and processes
• Solid understanding of the requirements within correct and timely documentation within a cGMP environment
Ihre Vorteile:
• Good infrastructure
• Varied tasks in a renowned international biotech company
Projektdauer: 12 MM++
Sie sind Freiberufler? Dann freuen wir uns auf Ihre Bewerbung!
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