GMP QC Lab Specialist: Equipment & Compliance

Novartis

Stein

Presencial

CHF 54 000 - 99 000

Tempo parcial

Há 3 dias
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Currículo e carta de apresentação personalizados, prontos a enviar.

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Vantagens oferecidas por esta oferta de emprego

Flexible working options where/when/if

Resumo da oferta

Novartis in Stein, Switzerland is seeking a part-time Quality Control Specialist I to support analytical laboratories. You will lead equipment maintenance and qualification activities, ensuring readiness for use and compliance in a GMP-regulated environment.

The role emphasizes collaboration with Quality, Manufacturing, and cross-functional teams, plus participation in investigations and continuous improvement while maintaining safety and quality practices.

Qualificações

  • Education in Chemistry, Biology, Biotechnology, Pharmacy or related field
  • First experience in a laboratory environment, preferably regulated industry
  • Basic understanding of GMP/GxP practices or willingness to learn

Responsabilidades

  • Perform lab equipment maintenance and qualification activities
  • Review and document maintenance and qualification activities
  • Coordinate with external service technicians for on-time execution with required quality
  • Maintain laboratory equipment and ensure readiness for use
  • Participate in investigations, troubleshooting, and continuous improvement
  • Contribute to KPI tracking and quality documentation
  • Collaborate with Quality, Manufacturing and cross-functional teams to ensure compliance and operational excellence
  • Follow HSE and quality requirements to maintain a safe and compliant environment

Conhecimentos

German (Fluent)
English (Basic)
Attention to detail
Communication skills
Collaboration
GxP/GMP awareness

Formação académica

Chemistry/Biology/Pharmacy or related field education

Descrição da oferta de emprego

Novartis in Stein, Switzerland is seeking a part-time Quality Control Specialist I to support analytical laboratories. You will lead equipment maintenance and qualification activities, ensuring readiness for use and compliance in a GMP-regulated environment.

The role emphasizes collaboration with Quality, Manufacturing, and cross-functional teams, plus participation in investigations and continuous improvement while maintaining safety and quality practices.

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