GMP QC Lab Specialist: Equipment & Compliance

Novartis; Stein; On-site; CHF 54,000 - 99,000; Part time

Benefits offered by this job

Flexible working options where/when/if

Job summary

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.

Qualifications

• 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

Responsibilities

• 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

Skills

German (Fluent)

English (Basic)

Attention to detail

Communication skills

Collaboration

GxP/GMP awareness

Education

Chemistry/Biology/Pharmacy or related field education

Job description

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.