QC Laboratory Analyst
Bekijk en reageer bij SIRE Life Sciences B.V. (externe link)
QC Laboratory Analyst (GMP, ELISA, PCR) voor een farmaceutisch bedrijf in Boxmeer, Noord-Brabant, start 31-07-2026.
- Locatie
- Boxmeer, Noord-Brabant
- Werkvorm
- op locatie
- Uren
- 32–40 uur per week
- Contractvorm
- detachering
- Startdatum
- Eerste waarneming
- Opdrachtgever
- A global pharmaceutical and animal health organization
Eisen
- Knowledge of biological testing techniques
- Strong communication skills in Dutch and English
- Minimum 3 years of experience in a Quality Control or GMP laboratory environment
- Knowledge of Lean and Six Sigma methodologies including Kaizen and structured problem solving
- MBO Level 4 qualification in Microbiology, Biology, or a related laboratory discipline
- Experience with ELISA, PCR, cell culture, microbiological testing, or similar laboratory methods
- Experience working under GMP regulations
Wensen
- Experience within the pharmaceutical industry
- Familiarity with SAP and electronic laboratory data systems
Omschrijving
The QC Laboratory Analyst is responsible for successfully transferring laboratory testing methods and ensuring high quality testing standards. The role supports the introduction of new products, transfer of existing testing methods between sites, and delivery of reliable quality control processes. Working within a GMP regulated environment, you will contribute to product quality, compliance, and operational excellence. Responsibilities include performing, reviewing, and reporting biological laboratory tests; conducting testing using ELISA, cell culture, titration, microbiological testing, PCR, and immunofluorescence techniques; entering and maintaining testing data within laboratory systems; reviewing, verifying, and releasing test results; supporting transfer of testing knowledge and methods to other laboratory locations; participating in operational meetings and team discussions; identifying, documenting, and reporting deviations according to established procedures; ensuring compliance with GMP, GGO, and EHS requirements; contributing to continuous improvement initiatives using Lean and Six Sigma methodologies; and supporting successful implementation of new testing methods and product launches. Requirements include an MBO Level 4 qualification in Microbiology, Biology, or a related laboratory discipline; a minimum of 3 years of experience in a Quality Control or GMP laboratory environment; experience working under GMP regulations; knowledge of biological testing techniques; experience with ELISA, PCR, cell culture, microbiological testing, or similar laboratory methods; familiarity with SAP and electronic laboratory data systems is preferred; strong communication skills in Dutch and English; experience within the pharmaceutical industry is preferred; and knowledge of Lean and Six Sigma methodologies including Kaizen and structured problem solving. Other information: focus on laboratory method transfer and validation, GMP regulated pharmaceutical setting.
Alle opdrachtenBekijk en reageer bij SIRE Life Sciences B.V. (externe link)
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