Work accurately in the laboratory while contributing to the quality of products that truly matter. As a QC Technician GC/HPLC at an organization specialized in chemicals, you will independently perform analytical analyses on raw materials, semi-finished products, and finished products for medical and pharmaceutical applications. You will work with techniques such as GC and HPLC, help develop and validate methods, and actively contribute to the continuous improvement of laboratory processes.
A role with substance, responsibility, and room for growth.
Profile
As a QC Technician GC/HPLC, you will be part of a small, dedicated quality team. You will collaborate with QA employees and a Senior QC Technician, and report to the Quality Manager. In your work, you will have regular contact with colleagues from Production, Purchase, Warehouse, and R&D, and sometimes also with suppliers, customers, and auditors.
What you will do.
- Perform chemical and physical QC analyses and process, interpret, and report the results.
- Sample and manage samples and laboratory supplies.
- Prepare and maintain work instructions, analysis reports, and quality documentation, including SOPs, work instructions, and batch records.
- Complete and sign QC documents such as logbooks, laboratory notes, and Certificates of Analysis (CoA's).
- Manage laboratory equipment, including calibration, maintenance, and supplier coordination.
- Identify deviations, solve laboratory issues, and contribute to safe work procedures and continuous improvement.
- Investigate raw materials, semi-finished products, and finished products using gas chromatography (GC), high-performance liquid chromatography (HPLC), and physical analysis methods.
- Actively contribute to the improvement of laboratory processes and quality documentation.
What they ask
- Completed MBO or HBO education in analytical chemistry or a comparable field.
- Experience with laboratory analyses; experience with GC and/or HPLC is a plus. Relevant internship experience is explicitly taken into account.
- Affinity with a production environment, preferably in the fine chemical or pharmaceutical industry.
- Familiarity with ISO 13485 and/or GMP is a plus, but not a requirement.
- Additional training or certification in QA/QC methodologies, such as Six Sigma Yellow Belt, is a plus.
- Good command of the Dutch and English languages.
- Accurate, takes initiative, and enjoys working independently.
- Seeks collaboration with colleagues within and outside the QA/QC team.
- Communicates clearly, thinks critically, and enjoys translating improvement ideas into concrete actions.
How to apply
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