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QA Officer (3/5 shifts) Baarle-Nassau • QTC Recruitment
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Engels (taal)
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Baarle-Nassau
Join a global pharmaceutical organisation as a QA Officer, where you'll play a vital role in ensuring the highest compliance standards for life-saving medicines. Be part of a close-knit QA team that supports batch release activities, contributing to patient safety worldwide. Benefit from a competitive salary with shift allowance, performance-related perks, and ample growth opportunities. Dive into a collaborative environment focused on learning, innovation, and making a significant impact on patient lives. Continue reading to discover why this job might be perfect for you.
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QTC Recruitment
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For our client, a global pharmaceutical organisation, we’re looking to recruit a QA Officer to support the QA department in batch release activities. This position is specifically interesting as you will absorb the knowledge of a global pharmaceutical organisation with many resources and opportunities. You’ll be part of a close-knit QA team that ensures each batch of life-saving medicine meets the highest compliance standards, directly contributing to patient safety and trust.
This is how you will make the difference
In this role, you will play a vital part in maintaining GMP compliance throughout production and release processes. You will ensure that all documentation, materials, and procedures meet regulatory and internal quality expectations. Your daily work will contribute to the timely release of high-quality pharmaceutical products reaching patients worldwide.
- Support the QA department in batch release and review documentation;
- Provide on-site QA support for daily operations and interventions;
- Ensure proper lifecycle management and archiving of all batch records;
- Release starting materials and incoming goods according to quality requirements;
- Conduct on-the-floor monitoring and participate in internal inspections;
- Approve and review operational procedures, protocols, and work instructions;
- Manage deviations and ensure timely completion of related actions;
- Support CAPA implementation and continuous improvement projects.
What you bring
You are someone who takes ownership, enjoys working in a dynamic GMP environment, and values precision and teamwork. Whether you come from a laboratory, manufacturing, or QA background, your curiosity and drive to learn will help you grow into a well-rounded QA professional.
- MBO or HBO education, preferably in a scientific or technical discipline;
- Understanding of GMP principles and quality systems;
- Eye for detail and strong organisational skills;
- Proactive attitude and ability to work accurately under time pressure;
- Willingness to work in shifts and be present on-site;
- Fluent in English (Dutch is a plus);
- Strong communication and problem-solving mindset.
What's in it for you
You will join a leading global organisation known for its high-quality standards, state-of-the-art facilities, and focus on employee growth. Expect a collaborative culture where your contribution is visible, valued, and rewarded.
- Competitive salary with significant shift allowance and performance-related benefits;
- Full-time, long-term position within a growing international environment;
- Extensive internal training and development opportunities;
- Exposure to advanced pharmaceutical production and release processes;
- Clear career paths and potential to progress within QA or other departments;
- Supportive team culture focused on learning and continuous improvement;
- Stable organisation with a strong purpose and patient impact.
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