Packaging/labeling Technician I

vor 18 Stunden


Allschwil, Schweiz Thermo Fisher Scientific Vollzeit

**Work Schedule**

7 1/2 hr shift

**Environmental Conditions**

Able to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed, Cold Room/Freezers -22degreesF/-6degrees C, Loud Noises (Equipment/Machinery), Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Standing for full shift, Strong Odors (chemical, lubricants, biological products etc.), Will work with hazardous/toxic materials

Effiziente, zeitgerechte und GMP-gerechte Vorbereitung, Durchführung und Abschluss von Herstellungs
- und Verpackungsauftragen ink. Durchführung von In Prozess-Kontrollen (PCs), sowie Durchführung der Reinigung von Ausrüstung und Maschinenteilen. Fachtechnische Führung der Produktionskabine.

**Aufgabenbereich**:

- Effiziente, zeitgerechte und GMP-gerechte Vorbereitung, Durchführung und Abschluss von Herstellungs
- und Verpackungsauftragen ink. Durchführung von ln prozess-Kontrollen (PCs)
- Fachtechnische Führung der Produktionskabine
- Effiziente und GMP-gerechte Durchführung der Reinigung von Ausrüstung
- und Maschinenteilen sowie von den Produktionsraumen
- GMP-gerechtes Dokumentieren der durchgeführten Arbeiten
- Einhaltung der spezifischen Vorschriften bei der Herstellung und Verpackung von klinischen Prof mustern, insbesondere der GMP-Regeln, Hygiene
- und Sicherheitsvorschriften und der jeweils relevanten Standardarbeitsanweisungen (SOPs) und Auftragsinstruktionen
- Sicherstellung der aktiven, zeitnahen und angemessenen Kommunikation von Fortschritten und Schwierigkeiten an den Kollegen und Vorgesetzten
- Aktive Mitarbeit bei der Identifizierung, Kommunikation und Losung von Problemen und Ineffizienz sowie bei Verbesserungsmoglichkeiten
- Mithilfe in spezifischen Projekten nach Anweisung vom Vorgesetzten
- Betreiben entsprechender Maschinen und Ausrüstungen
- Durchführen von TOE im GPM
- Selbständige einlesen von Komponenten
- Selbständige einbuchen von Fertigprodukt

**Qulifikation**:

- Abgeschlossene Lehre in einem für die Stelle relevanten Bereich
- Erfahrung in der Pharma
- oder Lebensmittelindustrie
- GMP-Erfahrung oder -Ausbildung van Vorteil
- Beherrschung der deutschen Sprache in Wort und Schrift. Englischkenntnisse van Vorteil
- Fähigkeit, Zeitvorgaben einzuhalten
- IT-Kenntnisse (Microsoft Office)
- Flexibilität zur Schichtarbeit



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