Vor 23 Tagen veröffentlicht

Senior QA Automation Specialist, EBR 80-100% (m/f/d)

Senior QA Automation Specialist, EBR 80-100% (m/f/d)

Senior QA Automation Specialist, EBR 80-100% (m/f/d)

Senior QA Automation Specialist, EBR 80-100% (m/f/d)

Lonza AG

Bio- und Nanotechnologie

Visp

  • Art der Anstellung: Vollzeit
  • 91.500 CHF – 116.500 CHF (von XING geschätzt)
  • Vor Ort
  • Noch schnell bewerben

Senior QA Automation Specialist, EBR 80-100% (m/f/d)

Über diesen Job

Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of.

What you'll get:

  • An agile career and dynamic working culture

  • An inclusive and ethical workplace

  • Compensation programs that recognize high performance

  • A variety of benefits dependant on role and location

What you'll do:

  • Partner with internal customers for quality topics linked to the set-up of eBR (electronic batch records) within the project.

  • Check and approve master production records and electronic master batch records (EMBR) for consistency with approval documents, process descriptions, transfer documents, test plans, and parameter lists.

  • Review completed batch records within the specified timeframe.

  • Review minor deviations, investigations, and CAPAs within the defined due dates.

  • Ensure that batch records are closed and archived when all batch-related activities are completed.

  • Assist in managing and tracking performance metrics and quality data, supporting QA department in various meetings.

  • Take on other tasks as assigned, ensuring seamless operations.

What we're looking for:

  • Academic degree in Chemistry/ Biotechnology/ Life Sciences or any related field is preferred, with equivalent experience considered.

  • Solid experience in the GMP-regulated pharmaceutical/API industry is required.

  • Experience in electronic batch records (execution and/or review) is preferred.

  • Ability to recognize non-compliance and gaps in quality standards.

  • Structured, detailed, and well-organized work attitude; open-minded to new ideas and suggestions; agile, highly motivated, and dynamic.

  • Business fluent English is required, good German language skills - an advantage.

This is a remarkable opportunity to work at Lonza AG, where your expertise will contribute to flawless operations and world-class quality management. We strictly adhere to the highest standards and are determined to successfully implement innovative solutions. Join us and be a part of an ambitious team that competes on a global scale!

Every day, Lonza’s products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.

People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.

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Bio- und Nanotechnologie

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