Sterile Drug Product Operator (2nd Shift)

Job-Room

Lalden

Vor Ort

CHF 75.000 - 95.000

Vollzeit

Vor 6 Tagen
Sei unter den ersten Bewerbenden
Bewerbungsgenerator

Mach aus dieser Rolle ein Vorstellungsgespräch — ein Lebenslauf und ein Anschreiben, die darauf ausgerichtet sind, was dieser Arbeitgeber sucht.

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Benefits dieser Stelle

Agile career
Inclusive workplace
Performance-based pay

Zusammenfassung

Lonza Visp, Switzerland is seeking Operators Biotechnologists with a relevant background to support growth across Life Sciences units. You will execute manufacturing activities in the Drug Product area, ensure batch execution per cGMP, and provide frontline technical support with the manufacturing team.

You will perform manual visual inspection of vials, prepare production documentation, operate and clean equipment, and maintain compliance with quality requirements.

Qualifikationen

  • Experience in a GMP-regulated environment, preferably Drug Product sterile manufacturing.
  • Familiar with GMP requirements, quality procedures and SOP execution.
  • Strong team orientation and collaborative mindset.
  • Excellent communication skills across functions.
  • Structured, proactive and highly motivated working approach.
  • Able to work in 2 shifts and flexible hours.

Aufgaben

  • Execute manufacturing activities in the Drug Product area per cGMP guidelines.
  • Perform manual visual inspection of liquid and lyophilized vials to ensure defect-free product.
  • Provide frontline technical and procedural support with the manufacturing team.
  • Ensure batches are produced safely, on schedule and in compliance.
  • Prepare production documentation (MBRs, forms) timely and accurately.
  • Operate, set up, and clean production equipment and premises.

Kenntnisse

GMP experience
Team oriented
Communication skills
Shift work
Flexible hours

Jobbeschreibung

Lonza Visp, Switzerland is seeking Operators Biotechnologists with a relevant background to support growth across Life Sciences units. You will execute manufacturing activities in the Drug Product area, ensure batch execution per cGMP, and provide frontline technical support with the manufacturing team.

You will perform manual visual inspection of vials, prepare production documentation, operate and clean equipment, and maintain compliance with quality requirements.

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