GMP Lab Technician — Mammalian Cell Processing

Aristo Group

Oberwallis

Vor Ort

CHF 65.000 - 90.000

Vollzeit

Vor 7 Tagen
Sei unter den ersten Bewerbenden
Bewerbungsgenerator

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Zusammenfassung

Aristo Group in Switzerland seeks a Lab Technician in Mammalian Processing to support upstream and downstream manufacturing in a GMP environment. You will perform laboratory testing, process monitoring, documentation, and troubleshooting to help deliver safe, compliant biopharmaceutical products.

You will work with Manufacturing, QA, QC, and Process Development teams, maintain equipment, ensure calibration, investigate deviations, and contribute to continuous improvement initiatives.

Qualifikationen

  • Apprenticeship or BSc in biotech, biology, chemistry, or related field.
  • Experience in GMP-regulated pharmaceutical or biotech lab.
  • English required; German is a plus.
  • Knowledge of mammalian cell culture preferred.

Aufgaben

  • Execute laboratory activities supporting mammalian cell culture manufacturing.
  • Perform sampling, in-process testing, and routine analytical assays.
  • Monitor process parameters and support batch execution.
  • Document activities in accordance with GMP and ALCOA+ requirements.
  • Maintain laboratory equipment and ensure calibration status.
  • Investigate deviations and support root cause analysis.
  • Collaborate with Manufacturing, QA, QC, and Process Development teams.
  • Contribute to continuous improvement and operational excellence initiatives.

Kenntnisse

Attention to detail
Teamwork
Good communication
Documentation discipline

Ausbildung

Apprenticeship or BSc in Biotechnology, Biology, Chemistry, or related field

Tools

Laboratory equipment familiarity
SAP
MES
LIMS
Electronic batch records

Jobbeschreibung

Aristo Group in Switzerland seeks a Lab Technician in Mammalian Processing to support upstream and downstream manufacturing in a GMP environment. You will perform laboratory testing, process monitoring, documentation, and troubleshooting to help deliver safe, compliant biopharmaceutical products.

You will work with Manufacturing, QA, QC, and Process Development teams, maintain equipment, ensure calibration, investigate deviations, and contribute to continuous improvement initiatives.

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