QA Technician

Cryoport Systems; Villers-le-Bouillet; Sur place; EUR 40 000 - 60 000; Plein temps

Avantages offerts par ce poste

Competitive salary

Meal vouchers

Hospitalization insurance

Equity

Résumé du poste

Cryoport Systems seeks a QA Technician in Belgium to help ensure GMP-compliant operations across the product lifecycle. With a life science degree and at least 2 years in pharma/biotech/CDMO QA or RA, you will manage QMS tasks, release batches, and support change controls while collaborating with cross-functional teams in an international environment.

Fluency in French and English (B2) and strong analytical skills are essential, as is the ability to work autonomously in a fast-changing setting

Qualifications

• A Bachelor’s degree in life science-related field.
• At least 2 years in pharma/biotech/CDMO QA or RA.
• Knowledge of GMP, GTP, GDP, HBM regulations and standards (ISO, ICH, EDQM).
• Strong analytical skills, attention to detail, and prioritization.
• Proactive, autonomous and adaptable to change.
• Fluency in French & English (B2 level preferred).
• Knowledge of Belgian Human Body Material regulations is a plus.

Responsabilités

• 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.

Connaissances

QA experience

GMP/GTP/GDP knowledge

Analytical skills

Attention to detail

Prioritization

Autonomy

Adaptability

French (B2)

English (B2)

HBM regulation knowledge

Formation

Bachelor’s degree in life science

Description du poste

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 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.

• competitive salary
• 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.