QA Batch Record Reviewer 80-100% (f/m/d)

Posted 2 Days Ago
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Visp, Valais
Entry level
Pharmaceutical
At Lonza, we enable A Healthier World by supporting our healthcare customers on the path to commercialization.
The Role
The QA Batch Record Reviewer is responsible for reviewing executed batch records, ensuring completeness of documentation, supporting batch release, initiating deviations, and evaluating KPI data. The role involves writing and revising SOPs and collaborating with various quality and operations functions to maintain cGMP compliance.
Summary Generated by Built In

 

Today, Lonza is a global leader in life sciences operating across three 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.

For our site in Visp we are looking for a QA Specialist, Batch Record Review (f/m/d) to extend our team. You will be part of the QA Operations Group Microbial and work in close collaboration with different quality and operations functions in order to ensure cGMP-compliant manufacturing activities and documentation.

Key responsibilities:

  • Review of the Executed Batch Records (e.g. cleaning logs, production documentation review, temperature reports, test procedures, raw data, logbooks)

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

  • Review comments added to the Executed Batch Records, clarify with the operations team and evaluate with the responsible QA Manager

  • Support the initiation of deviations and investigations for Batch Record Review related observations

  • Collect and evaluate on a regular basis KPI data

  • Support continuous improvement activities

  • Write and revise SOPs in area of expertise

Key requirements:

  • University Degree in Life Sciences e.g. Chemistry / Biotechnology or any other related field

  • First experience in the GMP regulated pharmaceutical / API production industry is an advantage

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

  • Experience collaborating closely with different functions and departments

  • Fluency in English language (written and spoken) and B1 (intermediate) German language skills are mandatory

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.

The Company
HQ: Basel
0 Employees
On-site Workplace
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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