QC Automation & Qualification Specialist II

C049 (FCRS = CH049) Novartis Pharma Schweizerhalle AG

Muttenz

On-site

CHF 72,000 - 134,000

Full time

2 days ago
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Benefits offered by this job

Hybrid work
Parental leave
Insurance plans
Retirement plans

Job summary

Novartis Pharma Schweizerhalle AG in Schweizerhalle, Switzerland, is seeking a motivated professional to strengthen the Laboratory Equipment Qualification team. This 2-year temporary role will support automation, AI, and qualification activities to ensure equipment and systems perform as intended and comply with GMP standards.

You will coordinate qualification activities with lab teams and stakeholders, author and review GMP-compliant documentation, and contribute to improvements in automation

Qualifications

  • Master’s degree in computer science, engineering, life sciences, or a related discipline with a strong technological focus.
  • Good understanding of chemical laboratory operations and workflows.
  • Independent, structured working style with proactive, solution-oriented thinking.
  • Experience in programming, automation, or the implementation of digital solutions.
  • Fluent in English and German.

Responsibilities

  • Coordinate and oversee the execution of change requests.
  • Author and review qualification documentation in accordance with GMP procedures.
  • Support improvements to laboratory automation systems and contribute to AI-related initiatives.
  • Coordinate qualification activities with laboratory teams and relevant stakeholders.

Skills

English fluency
German fluency
Programming
Automation experience
Digital solutions
Lab operations

Education

Master’s degree in CS/Engineering/Life sciences
PhD degree

Job description

Novartis Pharma Schweizerhalle AG in Schweizerhalle, Switzerland, is seeking a motivated professional to strengthen the Laboratory Equipment Qualification team. This 2-year temporary role will support automation, AI, and qualification activities to ensure equipment and systems perform as intended and comply with GMP standards.

You will coordinate qualification activities with lab teams and stakeholders, author and review GMP-compliant documentation, and contribute to improvements in automation

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