Join a global leader in Cell Therapy CDMO, where cutting-edge science meets collaboration to create groundbreaking therapies. As a QA Officer, you'll enhance your expertise in a fast-paced, GMP-compliant environment, ensuring quality assurance processes are met. Benefit from mentorship by senior QA staff and engage in diverse responsibilities, from batch record review to QA metrics tracking. Enjoy the dynamic setting of advanced therapy production with opportunities for professional growth. Learn about the growth opportunities available in this role.

Over het bedrijf

Panda International

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QA Officer
Geleen, Netherlands – Full-time

Company Description
For a global Cell Therapy CDMO, operating across five continents. We combine cutting-edge science with the power of collaboration to create technologies that help customers deliver breakthrough therapies to patients. In Geleen, our work supports the production of advanced therapies in a state-of-the-art GMP manufacturing environment.

Job Description
As QA Officer, you will support the daily execution of GMP-compliant operations by providing oversight and guidance in quality assurance processes. You will partner with internal teams to ensure documentation, batch records, and quality-related events meet regulatory standards. This is an ideal role for a QA professional with 2–3 years of experience looking to deepen their expertise within a fast-paced, highly regulated manufacturing setting.

You will report into the QA team and receive ongoing mentorship from senior QA staff to expand your knowledge of sterile operations, quality systems, and regulatory frameworks.

Key Responsibilities:

Review and prepare batch records for QP release and ensure timely resolution of related deviations, CAPAs, and change requests
Participate in QA on-the-floor activities, including witnessing and supporting GMP operations in production, QC, and warehouse areas
Review and approve GMP documents including SOPs, forms, master batch records, and protocols
Support QA metrics tracking and preparation of quality reports
Assist in the coordination of QA-related meetings and project updates
Ensure accurate documentation and closure of batch-related records
Flexibility to work in shifts when necessary to support timely batch disposition

Essential Requirements:

BSc or MSc degree in life sciences, biotechnology, or a related field
2–3 years of experience in a GMP-regulated QA role
Familiarity with batch record review and deviation/CAPA management
Experience working in a sterile environment is highly desirable
Strong attention to detail and ability to work cross-functionally
Fluent in English
Must hold a valid Dutch work permit

Additional Insights:

Location: Geleen, The Netherlands
Contract Type: Permanent
Start Date: ASAP

Sound interesting?
Send your CV to Khanyi Mabena at via de button "Solliciteer nu" op deze pagina. or reach out directly at +31 2020 44502.

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