Vacature - Jouw nieuwe functie

QA Officer (3/5 shifts)

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.

Details

Biotechnical

Quality/RA

Baarle-Nassau - Netherlands

40 uur per week

leer ons kennen

Jouw consultant

Sander Westerhout

+31 6 51 66 69 96 s.westerhout@qtcrecruitment.com

Over jouw rol

Zo maak jij het verschil

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.

Wat nodig is

Wat jij mee brengt

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.

Wat wij bieden

Jouw voordelen

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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