Department Info

At Terumo Europe, the Quality Assurance department plays a central role in ensuring that all manufacturing, testing, warehousing, and tech‑transfer activities meet the highest GMP and regulatory standards. Our QA Operations team partners closely with Manufacturing (OPS), Warehouse (WH), Quality Control (QC), and MSAT to safeguard product quality and patient safety.

This position is part of a dynamic, on‑the‑floor QA group that provides real‑time oversight and supports continuous improvement across the site.

The QA Operations Specialist ensures that daily GMP operations are executed in compliance with internal procedures and global regulatory expectations. You will provide hands‑on QA presence in manufacturing and warehouse areas, perform routine quality checks, support quality events, and manage material status in SAP.

Your work in our CDMO plant in Leverkusen directly contributes to the reliable supply of high‑quality biological products to patients worldwide. This position reports to Zhenda Whu, our Team Lead QA Operations

Job Responsibilities

• Provide daily GMP oversight across Manufacturing, Warehouse, QC, and MSAT, with a primary focus on OPS and WH.
• Conduct routine quality monitoring of production steps, logbooks, batch records, storage, and testing activities.
• Prepare batch documentation packages and perform real‑time batch record review on the shop floor.
• Inspect and release cleanrooms for GMP manufacturing.
• Perform AQL assessments following visual inspection activities.
• Oversee GMP activities for drug product manufacturing, including formulation, aseptic filling, lyophilization, visual inspection, and packaging.
• Handle abnormal or rejected materials physically and in SAP, including blocking/unblocking and maintaining material master data.
• Support Change Controls, Deviations, CAPAs, and other quality events.
• Review and revise SOPs, QRAs, and MBRs to drive continuous improvement.
• Perform electronic data review to ensure data integrity and compliance.
• Support self‑inspections, client audits, and authority inspections as SME and back‑office support.
• Take on additional responsibilities as assigned by the supervisor.

Profile Description

• Degree in Chemistry, Biochemistry, Microbiology, Molecular Biology, Biological Engineering, or a related field.
• Minimum 3 years of a proven track record in GMP in QA, QC, MSAT, or Manufacturing.
• Experience with biological product development or pharma manufacturing
• Strong knowledge of GMP and regulatory standards (EMA, FDA, ICH, WHO).
• Professional working proficiency in German and English
• Strong interpersonal, communication, and organizational skills.
• Proactive mindset with the ability to influence and drive improvement.
• Willingness to work in shift‑based schedules when required.
• Ability to pass a visual inspection qualification
• Proficiency with Microsoft Office and common digital tools.

Offer

• A meaningful role in a mission‑driven healthcare company that is in full expansion in Germany, improving patient outcomes worldwide.
• A collaborative, high‑quality GMP environment with strong cross‑functional interaction.
• Opportunities for professional development, training, and career growth.
• A culture that values integrity, teamwork, and continuous improvement.
• Competitive compensation and benefits aligned with Terumo Europe standards.

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