QC Analyst, Cell Therapy Quality (Ghent)

Legend Biotech US; Oost-Vlaanderen; On-site; EUR 42,000 - 62,000; Full time

Benefits offered by this job

Permanent contract

Attractive salary package with fringe.

Meal vouchers

Company laptop

Group and hospitalization insurance

End-of-year bonus

Performance bonus

Bicycle lease plan

4 days work, 4 days off

Job summary

Legend Biotech is expanding its Ghent Quality Operations team and seeks a QC Analyst to ensure high-quality CAR-T products. You will perform QC testing in IPC laboratories under GMP, monitor environmental conditions, collaborate with Quality and Operations, and manage data in our eLIMS system.

The role emphasizes documentation, SOP development, and continuous process improvements within a fast-paced biopharma environment. Fluency in Dutch and English is required.

Qualifications

• Bachelor’s degree in lab technologies or related field, or equivalent experience.
• Practical experience in aseptic production facility within QC or QA is a plus.
• Strong written and spoken communication in Dutch and English.

Responsibilities

• Perform QC testing for CAR-T products in IPC laboratories following GMP procedures.
• Conduct environmental monitoring by sampling (non-)viable particles and microorganisms to verify clean room classification.
• Collaborate with Quality and Operations to translate testing to production.
• Review and approve QC data, maintain documentation and manage results in eLIMS.
• Create and review QC documents, SOPs and work instructions; contribute to process improvements.

Skills

Dutch proficiency

English proficiency

Attention to detail

Quality mindset

Education

Bachelor's degree in lab technologies

Job description

Legend Biotech is expanding its Ghent Quality Operations team and seeks a QC Analyst to ensure high-quality CAR-T products. You will perform QC testing in IPC laboratories under GMP, monitor environmental conditions, collaborate with Quality and Operations, and manage data in our eLIMS system.

The role emphasizes documentation, SOP development, and continuous process improvements within a fast-paced biopharma environment. Fluency in Dutch and English is required.