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Benefits offered by this job
Diverse QC role with exposure to multiple laboratory processes
Opportunity for hands-on experience in Cell & Gene Therapy
Dynamic laboratory environment with emphasis on teamwork
Job summary
Lonza in Geleen, The Netherlands is seeking a QC Associate responsible for performing quality control activities in a GMP-regulated environment. The role requires a relevant degree and hands-on laboratory experience, especially in QC testing and microbiology. Responsibilities include routine QC activities, environmental monitoring, and documentation of test results. Ideal candidates will have good communication skills and strong attention to detail, motivated to work in a fast-paced and regulated environment.
Qualifications
Hands-on laboratory experience through work, internships or educational projects.
GMP knowledge or experience is considered a strong plus.
Accurate and structured way of working with strong attention to detail.
Responsibilities
Perform routine QC activities and laboratory assays in support of product release and GMP operations.
Document, review and report test results in line with GMP and data integrity standards.
Collaborate cross-functionally to ensure timely processing, testing and release activities.
Skills
Hands-on laboratory experience
Affinity with QC testing
Good communication skills in English
Education
MBO, HBO, BSc or MSc in Biotechnology, Microbiology, Life Sciences, Biomedical Sciences
Job description
Lonza in Geleen, The Netherlands is seeking a QC Associate responsible for performing quality control activities in a GMP-regulated environment. The role requires a relevant degree and hands-on laboratory experience, especially in QC testing and microbiology. Responsibilities include routine QC activities, environmental monitoring, and documentation of test results. Ideal candidates will have good communication skills and strong attention to detail, motivated to work in a fast-paced and regulated environment.