QA Automation Specialist - Batch Record Review (m/f/d) 80%-100%

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Visp, Valais, CHE
In-Office
Pharmaceutical
At Lonza, we enable A Healthier World by supporting our healthcare customers on the path to commercialization.
The Role

 

The actual location of this job is in VISP, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed.

At Lonza site in Visp we offer an outstanding opportunity for motivated individuals to join our team as a QA Automation Specialist (m/f/d) in Switzerland. In this role you will be working in close collaboration with different Quality and multiple Operations functions in order to ensure cGMP-compliant manufacturing activities and documentation within IBEX®.

A well-organized, agile and eager individual with basic GMP knowledge who possess a professional fluency of English and at least a basic level of German completes the profile.

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:

  • Review of the executed electronic batch records in MES Syncade

  • Involvement in MES Syncade Recipe change management

  • Collaborate with Operations team to clarify ambiguities in the executed batch records

  • Support in the management of Quality Records (CAPAs, Deviations/Investigations) for Batch Record review related observations

  • Support in batch release by ensuring the completeness of the documentation package

  • Interacting with the customer in batch record review and automation related topics

  • Collect and evaluate KPI data on a regular basis

What we are looking for:

  • University degree in Biology/Biotechnology/Life Science or similar educational background

  • Basic understanding of GMP and bioprocess manufacturing

  • Ability to identify non-compliance and gaps from Quality standards

  • Language Skills: Professional Fluency in English and basic German proficiency (A2), or willing to learn.

  • Structured, precise and well-organized working attitude; open-minded & pragmatic for new ideas and suggestions

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.

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The Company
HQ: Basel
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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