Join the Quality Assurance team as a QA Engineer in the pharmaceutical industry. You'll focus on maintaining high standards in qualification, calibration, and system data governance. Be a key player in audits and inspections, while supporting change control and system projects. Collaborate with cross-functional teams to ensure compliance and drive continuous improvement. Enjoy a hybrid work model and the chance to work with innovative systems like Comet and TruVault. Continue reading to see how you can make a difference in our team.

Over het bedrijf

Panda International

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Job Role: QA Engineer

About the Role
We are seeking an experienced QA Engineer to join our Quality Assurance team in Beerse, Belgium. This role focuses on qualification, calibration, maintenance, and system data governance within pharmaceutical manufacturing, ensuring compliance with quality and regulatory standards. You will review and approve qualification documentation, support change control and system introduction projects, and act as a key representative during audits and inspections.

Key Responsibilities

Review and approve qualification documentation (Impact Assessments, URS, DQ/IQ/OQ/PQ protocols & reports, QSRs, traceability matrices, etc.).
Ensure compliance of qualification activities and integration of quality standards into risk-based design reviews.
Review and approve calibration and maintenance records, certification master data, and system-related procedures.
Evaluate deviations, investigations, and CAPAs, ensuring effective corrective and preventive actions are implemented.
Review and approve Periodic System Quality Reviews (PSQRs) and Validation Master Plans (VMPs).
Ensure qualification deliverables are implemented into quality systems (SOPs, Work Instructions, Calibration Records, Maintenance Plans, etc.).
Support regulatory and customer inspections, acting as spokesperson for QA qualification-related matters.
Collaborate with cross-functional teams on system introduction, changes, and qualification projects to ensure compliance and timelines are met.
Drive continuous improvement and optimization of qualification processes.

Key Competencies

Strong knowledge of pharmaceutical legislation, cGMP regulations, and system qualification guidelines.
Analytical thinking, problem-solving, and risk assessment skills.
Effective communication and collaboration across teams and departments.
Ability to manage complexity, multiple priorities, and cross-department objectives.
Proactive mindset for innovation and continuous improvement.

Specific Know-How of Systems

Comet – incident handling and control of change system.
eStream – computerized maintenance management system.
TrüVault – document management system.
Summit – training system.
Kneat – digital validation lifecycle management.

Requirements

Master’s Degree in Engineering, Pharmacy, or equivalent.
5+ years of experience in the pharmaceutical industry.
Fluency in Dutch and English (written and spoken).
Familiarity with systems used in pharmaceutical manufacturing processes.

Practical’s

Location: Beerse, Belgium
Duration: end of 2025 (with potential extension)
Start Date: ASAP
Work Model: Full-time, Hybrid

Interested or know someone who might be?
Send your CV or inquiries to via de button "Solliciteer nu" op deze pagina. to apply or learn more.

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