Junior Bioprocess Operator – GMP Manufacturing (12m)

CK QLS

Luzern

Vor Ort

CHF 60.000 - 80.000

Vollzeit

vor 20 Stunden
Sei unter den ersten Bewerbenden
Bewerbungsgenerator

Eine vollständige Bewerbung in einer Minute — maßgeschneiderter Lebenslauf und Anschreiben, fertig zum Versenden.

Schaffe es an den ATS-Filtern vorbei

Zusammenfassung

CK QLS is seeking a Junior Production Operator to join a global Biopharmaceutical company in Lucerne on a 12-month contract. You will be part of the Biologics Manufacturing Science and Operations department, Drug Substance Bioprocess.

Key duties include equipment handling on the shop floor, GMP-compliant documentation, batch review, and coordinating daily work with cross-functional teams. Candidates should have 1 year in pharma/biotech, GMP familiarity, and strong German and English

Qualifikationen

  • 1 year of work experience in pharma/biotech or equivalent apprenticeship/education
  • Familiarity with GMP Manufacturing processes
  • Good communication skills in German and English (Verbal and Written)

Aufgaben

  • Support cross-functional team in running of equipment during manufacturing: Component preparation, equipment setup, sampling, material management, and other shop floor tasks
  • Maintain Equipment GMP Status: Routine monitoring, calibration, maintenance, and equipment certifications
  • Reviewing and completing batch documentation to support production activities
  • Reviewing / familiarization of area SOPs
  • Supports coordination of daily work schedules and effectively organizes with respective support groups
  • Inventory and order management

Kenntnisse

GMP manufacturing
German language
English language
Communication skills

Ausbildung

Pharma/biotech apprenticeship or education

Jobbeschreibung

CK QLS is seeking a Junior Production Operator to join a global Biopharmaceutical company in Lucerne on a 12-month contract. You will be part of the Biologics Manufacturing Science and Operations department, Drug Substance Bioprocess.

Key duties include equipment handling on the shop floor, GMP-compliant documentation, batch review, and coordinating daily work with cross-functional teams. Candidates should have 1 year in pharma/biotech, GMP familiarity, and strong German and English

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