Senior Quality Assurance Specialist Automation/EBR/BRR
vor 2 Wochen
At Lonza, we are seeking a highly skilled Quality Assurance Specialist to join our team in Visp. As a key member of our Vibe-X QA Operations team, you will be responsible for ensuring the buildup and execution of cGMP compliant manufacturing and documentation processes.
Key responsibilities include:
- Partnering with internal customers to address quality topics related to the setup of electronic batch records in the Vibe-X project.
- Reviewing and approving master production records and electronic master batch records for consistency with approval documents, process descriptions, transfer documents, test plans, and parameter lists.
- Reviewing executed batch records within defined timelines and ensuring that batch records are closed and archived when all batch-related activities are completed.
- Contributing to the management and tracking of Key Performance Indicators (KPIs) and quality metrics, and supporting the QA department in internal and external meetings.
Requirements include a Bachelor or Master of Science in chemistry, biotechnology, life sciences, or a related field, experience in the GMP-regulated pharmaceutical/API industry, and the ability to recognize non-compliance and gaps in quality standards.
We offer a dynamic and challenging work environment where you can make a meaningful difference in the lives of millions of people. If you are a motivated and organized individual with a passion for quality assurance, we encourage you to apply for this exciting opportunity.
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Visp, Schweiz Lonza VollzeitJoin Our Team as a Quality Assurance SpecialistWe are looking for a highly motivated and organized Quality Assurance Specialist to join our team at Lonza. As a Quality Assurance Specialist, you will be responsible for ensuring the quality of our products and processes.Key Responsibilities:Partner with internal customers to ensure quality topics are...
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