General information
Publication date
08/04/2026
Position description
Category
OPERATIONS - CONSULTING
Job title
QC Analyst - Life Sciences - M/F/X
Contract
Permanent contract
Job description
About the role
As QC Analyst, you will support laboratory operations focused on incoming materials and in-process samples. You will manage and test a range of primary and secondary components, as well as samples from in-process products, special tests, SQA, and MS&T. You will perform and document analytical measurements according to GLP and cGXP requirements while working in compliance with DI principles. The position combines hands-on laboratory work, data integrity responsibilities, and a strong focus on quality, safety, and continuous inspection readiness.
Key responsibilities
- Manage samples for incoming inspection, including primary and secondary components and materials from in-process products, special tests, SQA, and MS&T departments.
- Perform and document measurement tests on incoming and in-process samples in accordance with Good Laboratory
- Practices and applicable laboratory procedures.
- Maintain familiarity with and correctly apply the different measurement techniques used in the laboratory, ensuring consistent and reliable analytical results.
- Contribute to maintaining constant inspection readiness by following procedures, completing documentation accurately, and supporting audit-related activities when needed.
- Work according to established HSE safety procedures, detect and report potential incidents and risks, and propose practical solutions to reduce or eliminate these risks.
- Support laboratory investigations as required and, when assigned, take on responsibilities such as instrument owner, including being the point of contact for instrument issues and coordinating maintenance.
- Contribute to optimization projects related to laboratory operations, with focus on efficiency, quality, and data integrity, and support implementation of agreed improvements.
- Work to minimize lab errors, incidents, and invalid analyses due to human error, and support a culture of Right First Time (RFT) in both execution and documentation.
- Help keep IIA and WIP under control by understanding planning and priorities and acting accordingly to meet established deadlines without creating backlogs.
Business Industry
Life sciences
Profile
About you
- Practical experience or strong affinity with performing and documenting laboratory measurement tests in compliance with GLP requirements.
- Understanding of cGXP requirements and DI principles, with the ability to apply these consistently in daily laboratory work and documentation activities.
- Capability to become or act as SME (Subject Matter Expert) for specific analytical or measurement techniques and to support colleagues with technical questions.
- Strong focus on quality and accuracy, with the ability to work according to Right First Time (RFT) principles and minimize lab errors and invalid analyses.
- Awareness of HSE requirements and safe laboratory practices, including the ability to detect, report, and help resolve potential safety risks or incidents.
- Willingness to take on additional responsibilities such as instrument owner, On The Job Trainer, mentor, SOP reviewer using GdoC P software, archive owner, Data Integrity
- Expert/champion, or Safety Champion when assigned.
- !! Fluency in Dutch and English
Position location
Job location
Europe, Belgium, Flanders, Antwerp
Location
Noordkustlaan 16B 1702 Dilbeek
Candidate criteria
Level of experience
Recently Graduated