QC Scientist

LaCAR MDX Technologies; Luik; On-site; EUR 45,000 - 65,000; Full time

Benefits offered by this job

Dynamic environment

Training

Structured role with varied tasks

Fast-growing company

Enthusiastic team

Team events & atmosphere

Flexible hours & salary package

Permanent contract (38h/week)

HQ Belgium location in Sart-Tilman

Job summary

LaCAR is a fast-growing biotech company focused on CE-IVD diagnostic kits for genetics and newborn screening. We are seeking a QC Scientist to ensure quality, reliability, and robustness of analytical results in a regulated environment.

You will collaborate with Production, R&D, and QA, train technicians, and contribute to methods improvement. The role emphasizes hands-on QC work (ELISA, qPCR, MS), documentation, and CAPA-driven improvements within the Liège region.

Qualifications

• Bachelor or Master degree in chemistry or biochemistry.
• At least 3 years of experience in Quality Control within biotech/pharma or analytical lab.
• Strong hands-on experience with ELISA, qPCR, and mass spectrometry.
• Experience with antibody conjugation (HRP/Biotin) is a plus.
• Experience with Deviations, CAPA, Change Controls, OOS/OOT.
• Fluent English (minimum B2) and familiarity with ISO 13485/IVDR/FDA environments.

Responsibilities

• Perform QC analytical testing (ELISA, qPCR, MS) per procedures and quality standards.
• In-coming QC of raw material, in-process controls, and release testing to ensure batches meet specs.
• Analyze, interpret, and document results with accuracy and traceability.
• Draft and maintain QC docs, deviations, CAPA, change controls, and OOS/OOT investigations.
• Participate in non-conformity investigations and root-cause analysis.

Skills

ELISA

qPCR

Mass spectrometry

CAPA/Deviations

English (B2)

Autonomy

Education

Bachelor or Master in chemistry/biochemistry

Job description

Want to join a growing company in the biotech industry ?

Do you enjoy hands-on, structured work while participating in a variety of tasks ?

Willing to be part of a company advancing health and improving lives ?

At LaCAR, we are advancing health and improving lives.

LaCAR is continuing to grow and we are looking for a QC Scientist who is passionate about analytical laboratory work, values precision and reliability and is dedicated to ensuring the quality and consistency of final products.

You will work in a regulated environment and play a key role in customer satisfaction by guaranteeing the performance, compliance, and robustness of analytical results.

If you enjoy hands-on, structured work while participating in a variety of tasks, this opportunity is perfect for you!

Your Key Responsibilities:

• Perform quality control analytical testing, primarily ELISA, qPCR, and mass spectrometry, in accordance with established procedures and quality standards
• Conduct in-coming QC of raw material, In-Process Controls and release testing to ensure batches meet specifications
• Analyze, interpret, and document results while ensuring accuracy, traceability, and consistency
• Draft, review, and maintain QC documentation, including analytical reports, deviations, change controls, and OOS/OOT investigations
• Participate in non-conformity investigations, identify root causes, and contribute to corrective and preventive actions (CAPA)
• Ensure strict compliance with safety rules and Good Laboratory Practices
• Collaborate closely with Production, R&D, and Quality Assurance teams to support operational activities
• Train and mentor technicians or new team members on QC methods
• Contribute to continuous improvement of analytical methods

Who Are We?

LaCAR is a fast-growing biotech company developing, producing, and commercializing CE-IVD diagnostic kits for (pharmaco) genetics and newborn screening. Our headquarters are located in the Liège Science Park (Belgium), and we serve customers worldwide.

Who Are We Looking For?

• Bachelor or Master degree in chemistry or biochemistry
• At least 3 years of experience in Quality Control within the biotech/pharma industry or an analytical laboratory
• Strong hands-on experience with ELISA, qPCR, and ideally mass spectrometry
• Experience in antibody - HRP/Biotin conjugation and testing is a plus
• Highly rigorous, detail-oriented, and reliable in performing analytical tests
• Able to work autonomously while collaborating effectively with cross-functional teams
• Organized, versatile, and capable of managing multiple analyses simultaneously
• Experience with Deviations / CAPA / Change Controls / OOS / OOT
• Familiarity with regulated environments (ISO 13485, IVDR, FDA)
• Professional level of English (minimum B2)

Why Join Us?

• A dynamic and stimulating environment in the biotech sector
• Comprehensive training on procedures, equipment, and techniques
• A structured role with varied tasks, ideal for developing your expertise
• The opportunity to join an innovative and fast-growing company
• An enthusiastic team – Collaborative and open-minded in an international environment
• Fun team events & great atmosphere
• Flexible working hours & salary package
• Permanent contract (38h/week)
• Inspiring work environment (HQ Belgium)– Overlooking the woods of Sart-Tilman, with a south-facing terrace for afterwork events
• Free fruits & Free-Soup-Tuesdays