Lonza
life sciences
QCBatchReviewer
Neural analysis suggests this role is
optimal for Mid candidates.
“QC Batch Reviewer at Lonza. Skills: QC data review, GMP compliance, batch disposition. Review QC batch records, analytical data, raw data, chromatograms and calculations. Verify QC results against approved specifications, methods and GMP requirements”
What You'll Achieve.
ensuring the accuracy, completeness and compliance of QC data and batch documentation prior to product release; support compliant and timely batch disposition
Industry & Context.
Identify discrepancies, errors or non-conformances; Support investigations, root cause analysis and CAPAs
What They're Looking For.
Must Have
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, 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, 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
Nice to Have
Experience with electronic quality systems, ERP systems or digital documentation platforms is considered a plus
What You'll Do.
Review QC batch records
chromatograms and calculations
Verify QC results against approved specifications
methods and GMP requirements
Identify discrepancies
errors or non-conformances
Ensure appropriate follow-up actions are initiated
Support investigations
root cause analysis and CAPAs
Maintain accurate review documentation
Support inspection and audit readiness
Contribute to continuous improvement initiatives
How You'll Work.
Team & Collaboration
Work closely with QC, QA and Manufacturing teams; Collaborate with QC, QA and Manufacturing teams to resolve documentation or data-related issues; Daily collaboration with QC, QA and Manufacturing in a highly regulated environment
Communication Scope
Good communication skills in English
Full Job Description
## 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 *
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