Elevate Quality Assurance with Automation Expertise

vor 3 Wochen


Visp, Schweiz Lonza Vollzeit
Job Overview

As a QA Specialist Automation, you will be part of the Vibe-X QA Operations team at Lonza, responsible for ensuring the execution of cGMP compliant manufacturing and documentation processes. Your key responsibilities will include project-specific QA work regarding GMP products manufactured in the Vibe-X area, including reviewing executed batch records, minor deviations, and CAPAs within defined timelines. You will also partner with internal customers for quality topics linked to set-up eBR in the Vibe-X project and contribute to the management and tracking of Key Performance Indicators (KPI) and Quality metrics.

Requirements

To succeed in this role, you will need a Bachelor or Master of Science in chemistry, biotechnology, life sciences, or a related field. Experience in the GMP-regulated pharmaceutical/API industry is essential, as is the ability to recognize non-compliance and gaps in quality standards. A structured, precise, and well-organized work attitude, open-mindedness to new ideas, and agility are also key requirements. Preference will be given to candidates with experience working with electronic batch records (execution and/or review).

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