eyetec is a trusted partner for healthcare industries
With more than twenty years’ experience in technical pharmaceutical manufacturing, eyetec perfectly understands the challenges companies in the pharmaceutical industry, hospitals and pharmacies face.
our services
eyetec is a leading international expert in visual inspection and container closure integrity testing (CCIT). In addition, eyetec provides a vast array of services for the healthcare sector. These include sales, design, maintenance, calibration, and qualification support of pharmaceutical manufacturing equipment.
eyetec is renowned for visual inspection and CCIT, ensuring compliance, technical and operational efficiency of the production process of parenteral pharmaceutical products.
positive controls
consultancy
vision engineering
pharma equipment
eyetec is the official Benelux distributor and after-sales partner for several high-quality pharmaceutical machine brands.
equipment sales
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after-sales support
qp and qa services
eyetec offers QP services mainly for the ATMP and biotech sectors. We can also act as interim QA manager or follow up on limited assignments.
qp and qa services
in the spotlight
Visual Inspection & CCIT
Visual Inspection for Difficult-to-Inspect Products
Particle seeding in Infusion Bags & tailored consultancy services
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jobs
Lab Operator
We are looking for a motivated ‘Lab Operator'.
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QA QP
Understanding the role of a Quality Assurance Officer at eyetec
In the pharmaceutical industry, where the quality of products can significantly impact patient health, the role of a quality assurance (QA) officer is crucial. At eyetec, the role of a QA officer encompasses various crucial functions to uphold the highest standards of product quality and safety. We recently sat down with Jolien, our dedicated QA officer at eyetec, to delve into her daily responsibilities, the challenges she faces, and the critical importance of QA in the realm of pharmaceutical production.
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eyetec is a trusted partner for healthcare industries
Because of its combined experience in both compliance as well as technical aspects of pharmaceutical manufacturing, backed up by more than twenty years of experience in GMP manufacturing.
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