QC batch reviewer

QC Batch Reviewer
 

Geleen, Netherlands
 

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

As a QC Batch Reviewer, you play a key role in ensuring the accuracy, completeness and compliance of QC data and batch documentation prior to product release. You work closely with QC, QA and Manufacturing teams to support compliant and timely batch disposition within a GMP-regulated environment.
 

What you will get

• A central role in reviewing and approving QC data before product release
• Exposure to a broad range of QC techniques, analytical data and GMP documentation
• Daily collaboration with QC, QA and Manufacturing in a highly regulated environment
• The opportunity to develop expertise in batch review, investigations and GMP compliance
• A role with high visibility and direct involvement in operational decision-making
• Compensation programs that recognize high performance
   

What you will do

• Review QC batch records, analytical data, raw data, chromatograms and calculations for accuracy, completeness and compliance
• Verify QC results against approved specifications, methods and GMP requirements
• Identify discrepancies, errors or non-conformances and ensure appropriate follow-up actions are initiated
• Collaborate with QC, QA and Manufacturing teams to resolve documentation or data-related issues
• Support investigations, root cause analysis and CAPAs related to QC data and batch documentation
• Maintain accurate review documentation and support inspection and audit readiness
• Contribute to continuous improvement initiatives within QC and batch review processes
   

What we are looking for

• Bachelor’s or Master’s degree in Chemistry, Biochemistry, Pharmacy, Biotechnology or a related scientific field
• Minimum of 3 years of experience in QC, QA or batch record review within a GMP-regulated pharmaceutical or biotechnology environment
• Strong understanding of cGMP regulations, quality systems and regulatory requirements
• Experience reviewing analytical data such as HPLC, flow cytometry, cell count, UV/Vis or microbiological testing
• Strong attention to detail and the ability to work accurately with complex documentation
• Good communication skills in English and the ability to collaborate across multiple departments
• Experience with electronic quality systems, ERP systems or digital documentation platforms is considered a plus
   

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.

Swiss contract development and manufacturing organization (CDMO) providing biologics, cell, and gene therapy production services.

lonza.com