Entry-Level QC Microbiology Analyst

Lonza

Oberwallis

Vor Ort

Vertraulich

Vollzeit

vor 20 Stunden
Sei unter den ersten Bewerbenden
Bewerbungsgenerator

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Benefits dieser Stelle

Agile career
Inclusive workplace
Competitive hourly rate

Zusammenfassung

Lonza in Visp is seeking an enthusiastic laboratory technician to join the QC Microbiology team. You will perform microbial identifications and endotoxin measurements, ensuring medicines meet the highest quality standards. The role is fully site‑based with a 12‑month contract and 41 hours per week.

Entry‑level candidates and new graduates are welcome. You will document activities in GMP‑compliant systems, support production schedules, and collaborate across QC teams.

Qualifikationen

  • Entry-level candidates welcome.
  • Solid foundation in microbiology techniques.
  • Experience with endotoxin testing preferred.
  • Familiarity with LIMS/MODA systems.
  • Ability to work under time pressure with high precision.

Aufgaben

  • Perform daily QC analyses focusing on microbial identifications and endotoxin measurements.
  • Process time-critical samples with 24-hour turnover to support production schedules.
  • Document laboratory activities per GMP and internal guidelines; maintain safety compliance.
  • Execute analytical methods, review data, create protocols, testing instructions, and short reports.
  • Enter and release analytical results using digital platforms including LIMS and MODA.

Kenntnisse

Microbiology basics
Quality control
Time management
German language (spoken/written)

Ausbildung

Bachelor's degree in Biology/Microbiology
Laboratory Technician Apprenticeship

Tools

LIMS
MODA

Jobbeschreibung

Lonza in Visp is seeking an enthusiastic laboratory technician to join the QC Microbiology team. You will perform microbial identifications and endotoxin measurements, ensuring medicines meet the highest quality standards. The role is fully site‑based with a 12‑month contract and 41 hours per week.

Entry‑level candidates and new graduates are welcome. You will document activities in GMP‑compliant systems, support production schedules, and collaborate across QC teams.

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