Intern - QA Specialist Batch Record Review

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

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.

• Bachelor degree or relevant work/ internship experience in Biology, Chemistry, Biotechnology, Life Science or other related field

• Previous experience in GMP regulated pharmaceutical / API industry is an advantage

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

• Structured, precise and well-organized working attitude; open-minded for new ideas and suggestions; agile, highly motivated and dynamic drive

• English: Fluent. German: Good to have.