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Lonza

9 Month FTC - Quality Batch Consolidator

Job Posted 22 Days Ago Posted 22 Days Ago
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Slough, Berkshire, England
Mid level
Slough, Berkshire, England
Mid level
The Quality Batch Consolidator performs auditing duties related to QC testing for Drug Products and Drug Substances, ensures compliance with regulations, and facilitates communication between departments.
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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.

The Role:

The role of the Quality Batch Consolidator is to perform Batch Consolidation (auditing) duties regarding QC Biochemistry and QC Microbiology testing activities for Drug Product (DP) and Drug Substance (DS). The role requires the incumbent to coordinate the consolidation of all the QC testing activities and to perform an independent check that all the relevant activities have been completed and all release specifications have been met.

Please note that this is a 9-month FTC

Key responsibilities:

  • Liaise with internal customers to ensure they receive the information they require and maintain effective interdepartmental communication and collaboration.

  • Work with the QC Analysts, Manager and Team Leaders to enable continued improvement of QC quality systems/processes.

  • To continually identify and implement improvements in safety, GMP compliance and efficiency.

  • Raise and complete Deviation / CAPA / Change Control as determined by the Line Manager.

  • Perform Batch Consolidation duties with regard to QC Biochemistry and Microbiology testing activities for Drug Products and Drug substances.

  • Perform audits of the laboratory as determined by the Line Manager.

  • Assist with preparatory work before audit and the provision of QC-related information during customer and regulatory audits

Key requirements:

  • Knowledge of Regulatory and cGMP guidelines, release and stability testing, and quality auditing experience in a GMP environment

  • Utilising knowledge of quality procedures to identify and report non-conformances and resolve issues arising in the area.

  • Perform other duties as assigned/ required

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.

Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.

Top Skills

Gmp

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