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Salary
≈ $21k – $48k per year (Estimated)
Location
In office (Villers-le-Bouillet)
Seniority
Junior · 2+ years exp
Employment
Full-Time

First seen by Alion on Aug 12, 2026.

Overview
Company
Impact
Profile match
Learn how Cryoport Systems' comprehensive platform helps deliver certainty throughout the life sciences supply chain.

Cryoport Systems is a comprehensive supply chain partner for the life sciences industry, delivering specialized solutions to meet the challenges of the biopharmaceutical, cell and gene therapy, reproductive medicine, and animal health markets. Our offerings span logistics, BioServices and biostorage, cryopreservation, and consulting, ensuring the highest standards of quality and reliability for sensitive materials. With our expansive platform of management solutions and decades of temperature-controlled supply chain expertise, Cryoport Systems helps Enable the Outcome™ by supporting certainty and precision in the supply chain, whether advancing groundbreaking therapies, supporting families on their reproductive journeys, or enhancing animal health programs.

Are you passionate about quality assurance in the biotech sector? Do you want to contribute to a meaningful mission-advancing therapies in the fight against cancer? As a QA Technician, you’ll ensure compliance with international, European, and local regulations while supporting operational activities within a dynamic and innovative environment.

What we expect from you :

  • Implementing and maintaining the local QMS: Ensuring compliance with global and local quality management systems to drive continuous improvement.

  • Providing QA oversight for the product and process lifecycle: Monitoring performance, identifying quality trends, and addressing deviations, CAPAs, and change controls.

  • Reviewing operational documentation: Collaborating with operational teams to review forms, batch records, and labels.

  • Releasing batches: Approving incoming materials and final products.

  • Training follow-up: Ensuring personnel receive appropriate training and maintaining training matrices.

We're looking for someone with :

  • A Bachelor’s degree in a life science-related field.

  • At least 2 years of experience in a pharmaceutical, biotech, or CDMO environment, in a QA or RA role.

  • Knowledge of GMP, GTP, GDP, HBM regulations and standards (ISO, ICH, EDQM).

  • Strong analytical skills, attention to detail, and the ability to anticipate impacts and set priorities.

  • A proactive attitude, with the ability to work autonomously and adapt to a fast-changing environment.

  • Fluency in French & English (B2 level preferred).

  • Knowledge of Human Body Material Belgian legislation is a plus.

What we offer :

Our offices in Villers-le-Bouillet (Belgium) offer amodern and ergonomic workspace, ideally located betweenLiège and Namur, with easy highway access. Since moving into ourbrand-new facilities in November 2023, we’ve created a comfortable & ergonomic environment. We foster afriendly and engaging atmosphere, regularly organizingbreakfasts and team events because we believe a positive work environment matters. As part of aglobal group, you’ll operate in aninternational environment, usingEnglish daily to collaborate across sites,broadening your perspective on different cultures and ways of working. We offer acompetitive salary with extra-legal benefits (meal vouchers, hospitalization insurance, equity and more). Most importantly, you'll contribute to a meaningful mission-advancing therapies in the fight against cancer.

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