QC Laboratory Analyst

SIRE LIFE SCIENCES; Boxmeer; On-site; EUR 42,000 - 60,000; Full time

Job summary

SIRE LIFE SCIENCES is seeking a QC Laboratory Analyst in Boxmeer, Netherlands, to transfer testing methods, perform ELISA, PCR, cell culture, and release results within a GMP setting.

You will support method transfers, data entry, and continuous improvement initiatives, with emphasis on accuracy, documentation, and collaboration across sites.

Qualifications

• Minimum 3 years of experience in a Quality Control or GMP laboratory environment.
• Experience working under GMP regulations and knowledge of biological testing techniques.
• Strong communication skills in Dutch and English.

Responsibilities

• Perform, review, and report biological laboratory tests.
• Conduct ELISA, cell culture, titration, microbiological testing, PCR, and immunofluorescence techniques.
• Enter and maintain testing data within laboratory systems.
• Review, verify, and release test results.
• Support transfer of testing knowledge and methods to other laboratory locations.
• Participate in operational meetings and team discussions.
• Identify, document, and report deviations according to procedures.
• Ensure compliance with GMP, GGO, and EHS requirements.
• Contribute to continuous improvement initiatives using Lean and Six Sigma methodologies.
• Support implementation of new testing methods and product launches.

Tools

SAP

ELISA

PCR

Cell culture

Electronic laboratory data systems

Job description

The Company

A global pharmaceutical and animal health organization focused on developing innovative medicines and vaccines. The company operates large scale research, manufacturing, and quality operations, with a strong commitment to quality, safety, sustainability, and continuous improvement.

Role Description

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

• Perform, review, and report biological laboratory tests
• Conduct testing using ELISA, cell culture, titration, microbiological testing, PCR, and immunofluorescence techniques
• Enter and maintain testing data within laboratory systems
• Review, verify, and release test results
• Support transfer of testing knowledge and methods to other laboratory locations
• Participate in operational meetings and team discussions
• Identify, document, and report deviations according to established procedures
• Ensure compliance with GMP, GGO, and EHS requirements
• Contribute to continuous improvement initiatives using Lean and Six Sigma methodologies
• Support successful implementation of new testing methods and product launches

Requirements

• MBO Level 4 qualification in Microbiology, Biology, or a related laboratory discipline
• Minimum 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
• 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

58581