Quality Control Analyst I — GMP & Lab Support

Novartis

Stein

Vor Ort

CHF 75.000 - 110.000

Vollzeit

vor 44 Stunden
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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Zusammenfassung

Novartis is seeking a Quality Operations associate to support the quality department's activities, ensuring compliant execution of systems and documentation across the lab. You will contribute to the implementation, maintenance, and operation of quality and/or lab systems.

You will follow SOPs, assist in document creation, report technical issues within 24 hours, and collaborate across teams to sustain GMP standards and regulatory compliance.

Qualifikationen

  • Provides technical and/or administrative support for the quality organization.
  • Follows SOPs and/or laboratory methods in an effective and compliant manner.
  • Assists in creating documents (reports, records, presentations).
  • Reports technical complaints / adverse events / special-case scenarios related to Novartis products within 24 hours of receipt.

Aufgaben

  • Provides technical and/or administrative support for the quality organization.
  • Performs simple, routine, and repetitive activities as directed by supervisor.
  • Follows SOPs and/or laboratory methods in an effective and compliant manner.
  • Assists in creating documents (reports, records, presentations).
  • Reports technical complaints / adverse events / special-case scenarios within 24 hours of receipt.
  • Distributes marketing patterns when applicable.

Kenntnisse

Quality Assurance (QA)
GMP procedures
Quality standards
Quality control (QC) testing
Dealing with ambiguity
Self-awareness
Continuous learning
Technological know-how

Jobbeschreibung

Novartis is seeking a Quality Operations associate to support the quality department's activities, ensuring compliant execution of systems and documentation across the lab. You will contribute to the implementation, maintenance, and operation of quality and/or lab systems.

You will follow SOPs, assist in document creation, report technical issues within 24 hours, and collaborate across teams to sustain GMP standards and regulatory compliance.

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