Job Description

Responsibilities

Taking care of the quality management software as system administrator.

  • Support and train users.
  • Improve and update processes including relevant SOPs and documents.
  • Harmonize processes.
  • Lead projects.
  • Implement additional modules and functionalities within the quality management software.

Qualifications

  • Background in analytical chemistry, biochemistry, or life science.
  • Experience in the analytical‑pharmaceutical environment, preferably in QA.
  • Skills to solve problems and build good relationships with stakeholders.
  • Good interpersonal skills and teamwork spirit.
  • Ability to collaborate in a dynamic, cross‑functional matrix environment.
  • Ability to lead projects between sites and work independently.
  • Broad knowledge and proven experience of the regulatory framework in the GMP environment (ICH, FDA, USP, Ph.).
  • ...

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