QA Technician
CryoPort Systems
This listing was originally posted on CryoPort Systems's careers page. Formulate is an equal opportunity job aggregator and is not involved in the hiring process. Where salary information is estimated, it is derived from BLS industry benchmarks and may differ from actual compensation.
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Upgrade to Pro — $25/moCryoport Systems is the life science industry’s most trusted provider of supply chain solutions for temperature-sensitive materials, serving biopharmaceutical, IVF and surrogacy and animal health organizations around the world. Cryoport Systems' proprietary Cryoport Express® shippers, Cryoportal® Logistics Management Platform, leading-edge Smartpak™ Condition Monitoring System and geo-sensing technology paired with unparalleled logistics expertise and 24/7/365 customer support, make Cryoport Systems the end-to-end temperature controlled supply chain partner that you can trust.
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.
A first successful 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.
The willingness to work in a 2 to 3 shifts schedule.
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 a modern and ergonomic workspace, ideally located between Liège and Namur, with easy highway access. Since moving into our brand-new facilities in November 2023, we’ve created a comfortable & ergonomic environment. We foster a friendly and engaging atmosphere, regularly organizing breakfasts and team events because we believe a positive work environment matters. As part of a global group, you’ll operate in an international environment, using English daily to collaborate across sites, broadening your perspective on different cultures and ways of working. We offer a competitive 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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BIOTECHNOLOGY
Temperature-controlled supply chain solutions
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