QA Operations Specialist (m/f/d)

QA Operations Specialist (m/f/d)

Leverkusen Vollzeit 63000 - 77000 € / Jahr (geschätzt) Kein Homeoffice möglich
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Auf einen Blick

  • Aufgaben: Sichere die Qualität in der Produktion und im Lager durch tägliche GMP-Überwachung.
  • Unternehmen: Terumo, ein wachsendes Unternehmen im Gesundheitswesen mit einem klaren Fokus auf Patientenwohl.
  • Vorteile: Wettbewerbsfähige Vergütung, Entwicklungsmöglichkeiten und ein unterstützendes Team.
  • Weitere Informationen: Dynamisches Arbeitsumfeld mit starken Möglichkeiten zur beruflichen Weiterentwicklung.
  • Warum dieser Job: Gestalte die Zukunft der Gesundheitsversorgung und mache einen echten Unterschied für Patienten weltweit.
  • Qualifikationen: Abschluss in Biochemie oder verwandten Bereichen und Erfahrung in GMP.

Das prognostizierte Gehalt liegt zwischen 63000 - 77000 € pro Jahr.

QA Operations Specialist (m/f/d) Apply now " At Terumo, we advance lifesaving medical technologies to benefit society.

Are you eager to make a difference with us?

Here, you'll grow your expertise while staying true to your personal aspirations.

Guided by our Japanese heritage, we act with respect, take ownership, and pursue continuous improvement.

If you see yourself in our values, keep reading; this might be the opportunity you're looking for

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.

Job Summary

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.
  • Contact Person

Jan Swinnen - Talent Acquisition Lead Note: Please submit applications in English through the link provided in this job advertisement.

Working at Terumo means advancing healthcare with heart.

Here, you are empowered to grow your own way, inspired to create to innovate, and supported as we get there together.

Join us in shaping a healthier future for our patients, society, and each other.

Apply now "

QA Operations Specialist (m/f/d) Arbeitgeber: TERUMO Deutschland GmbH

Terumo ist ein hervorragender Arbeitgeber, der Ihnen die Möglichkeit bietet, in einem hochmodernen, sterilen Produktionsumfeld zu arbeiten, in dem Qualität und Compliance an erster Stelle stehen. Unsere Unternehmenskultur fördert Zusammenarbeit, kontinuierliche Verbesserung und persönliche Entwicklung, während wir gemeinsam an der Verbesserung der Gesundheitsversorgung arbeiten. In Leverkusen haben Sie die Chance, Ihre Führungsfähigkeiten auszubauen und Teil eines engagierten Teams zu werden, das sich für lebensrettende Technologien einsetzt.

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Kontaktdaten:

TERUMO Deutschland GmbH Recruiting-Team

Wir glauben, dass du diese Fähigkeiten brauchst, um QA Operations Specialist (m/f/d) mit Bravour zu bestehen

GMP-Kenntnisse
Qualitätskontrolle (QC)
Materialstatusmanagement in SAP
Batch-Dokumentation
AQL-Bewertungen
Änderungskontrollen
Deviationen