Quality Control Analyst
Bekijk en reageer bij SIRE Life Sciences B.V. (externe link)
Quality Control Analyst (QC) voor een wereldwijde Animal Health organisatie in Boxmeer, tijdelijke opdracht voor laboratoriumtesten in een GMP-omgeving.
- Locatie
- Boxmeer
- Werkvorm
- op locatie
- Uren
- 40 uur per week
- Contractvorm
- detachering
- Sluitingsdatum
- Eerste waarneming
- Opdrachtgever
- Animal Health organization
Eisen
- Accurate, proactive, organized, and quality-oriented, with the ability to work independently and collaboratively in a regulated laboratory environment.
- Relevant experience in QC laboratory testing, preferably within pharmaceutical, biotech, or Animal Health environments.
- Good knowledge of GMP, Good Documentation Practices, and data integrity.
- Fluent in Dutch, both written and spoken, is mandatory, with a good command of English.
- MBO/HBO degree in Chemistry, Biochemistry, Microbiology, Biotechnology, Life Sciences, or a related field.
Omschrijving
The Company A leading global Animal Health organization dedicated to improving animal health and well-being through innovative pharmaceuticals, vaccines, and health solutions. The company offers an international environment with opportunities for professional growth, collaboration, and continuous learning.
Role Overview We are seeking a Quality Control Specialist / QC Analyst to perform laboratory testing and support QC activities within a GMP-regulated environment. The role focuses on testing and reporting results for production, stability, and batch-release activities, while supporting deviations, documentation, equipment, and continuous improvement.
Key Responsibilities - Perform routine QC laboratory testing, verify results, and accurately document and report findings. - Identify and escalate deviations, abnormal results, and trends, supporting GMP investigations where required. - Support test transfers, validation activities, and continuous improvement projects. - Maintain laboratory equipment, including cleaning, calibration, and maintenance. - Create and update QC Work Instructions and GMP documentation, and participate in audits. - Collaborate with QC, QA, Operations, Engineering, and other stakeholders; support training of new employees and interns and communicate effectively in Dutch.
Requirements - MBO/HBO degree in Chemistry, Biochemistry, Microbiology, Biotechnology, Life Sciences, or a related field. - Relevant experience in QC laboratory testing, preferably within pharmaceutical, biotech, or Animal Health environments. - Good knowledge of GMP, Good Documentation Practices, and data integrity. - Fluent in Dutch, both written and spoken, is mandatory, with a good command of English. - Accurate, proactive, organized, and quality-oriented, with the ability to work independently and collaboratively in a regulated laboratory environment.
Other Information Interested in this opportunity? Click Apply to learn more and become part of a global Animal Health organization where you can develop your QC and GMP expertise while contributing to high-quality products.
Location: Boxmeer, Noord-Brabant | Sector: Pharmaceuticals | Start Date: 8/24/2026 | Job ref: 58769
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