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

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Visp, Valais
In-Office
80-100 Annually
Senior level
Pharmaceutical
At Lonza, we enable A Healthier World by supporting our healthcare customers on the path to commercialization.
The Role
Oversee and ensure quality management for eBR systems, review batch records, manage quality metrics, and collaborate with internal teams in a regulated pharmaceutical environment.
Summary Generated by Built In

 

Location: the actual location of this job is in Visp, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed.

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!

What you will get:

  • An agile career and a dynamic work culture.

  • An inclusive and ethical workplace.

  • Compensation programs that recognize high performance.

In addition to a competitive salary, you can expect numerous lifestyle, family, and leisure benefits. Our full list of tailored local benefits can be found below.

Benefits in Visp: https://bit.ly/3wjkoFi  

What you will 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 are 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.

About Lonza

At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone’s ideas, big or small, have the potential to improve millions of lives, and that’s the kind of work we want you to be part of.

Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we value diversity and are committed to creating an inclusive environment for all employees. If you’re ready to help turn our customers’ breakthrough ideas into viable therapies, we look forward to welcoming you on board.

Ready to shape the future of life sciences? Apply now.

Top Skills

Electronic Batch Records
Gmp
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The Company
HQ: Basel
0 Employees
Year Founded: 1897

What We Do

At Lonza, we enable A Healthier World by supporting our healthcare customers on the path to commercialization. Our community of 16,000 talented employees work across a global network of more than 30 sites to deliver for our customers across the pharma, biotech and nutrition markets.

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