Quality Assurance Specialist for Pharmaceutical Manufacturing

vor 3 Wochen


Visp, Schweiz Lonza Vollzeit

Role Summary
In this role, you will be responsible for ensuring the quality and compliance of our pharmaceutical manufacturing processes. You will work closely with our operations team to develop and implement cGMP compliant manufacturing and documentation processes.

Key Responsibilities:

  • Partner with internal teams to ensure quality standards are met for GMP products manufactured in the Vibe-X area.
  • Review and approve master production records, electronic master batch records, and batch records to ensure consistency with approval documents and process descriptions.
  • Contribute to the management and tracking of Key Performance Indicators (KPIs) and Quality metrics.
  • Perform other duties as assigned by the QA team lead.

Requirements:

  • Bachelor or Master of Science in chemistry, biotechnology, life sciences, or a related field.
  • Experience in the GMP-regulated pharmaceutical industry.
  • Ability to recognize non-compliance and gaps in quality standards.
  • Structured work attitude, open-minded to new ideas, and highly motivated.


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