Laboratory Analyst

DPS Group Global; Puurs; On-site; EUR 42,000 - 64,000; Full time

Job summary

DPS Group Global is seeking a Laboratory Analyst to perform routine and specialized analyses in a pharmaceutical manufacturing setting. You will conduct HPLC/UPLC tests on biological molecules, CGE, ELISA, and particle analysis per SOPs, while supporting process development and investigations.

You will help maintain the lab, ensure safety standards, calibrate equipment, and support method validation, sample handling, and KPI monitoring across projects.

Qualifications

• Experience performing HPLC/UPLC analysis in pharmaceutical/biotech settings.
• Working knowledge of GLP, SOPs and quality systems.
• Proficiency with laboratory information management systems and common PC software.
• Ability to troubleshoot analytical issues and support method development.

Responsibilities

• Perform routine and specialized tests (HPLC/UPLC, CGE, ELISA, particle analysis) per SOPs and protocol.
• Maintain lab environment, ensure safety, and calibrate/maintain equipment for development work.
• Support analytical method validation, sample processing, and reagent inventory management.
• Handle administrative tasks and monitor KPIs in the laboratory.

Skills

HPLC/UPLC analysis

CGE

ELISA

Particle analysis

MS Office

LIMS

Empower platform

Tools

LIMS

Empower platform

MS Office

Job description

As a Laboratory Analyst you will be conducting a wide range of laboratory analyses, within a pharmaceutical manufacturing setting, ensuring accuracy and compliance with current standards and procedures.

Responsibilities

• Performing routine and specialized tests such as HPLC/UPLC analysis on biological molecules, CGE, ELISA, particle analysis, ... according to Standard Operating Procedures (SOPs) and supporting process development work and root cause investigations according to protocols
• Maintaining the laboratory environment, ensuring safety specifications, and overseeing the maintenance and calibration of laboratory equipment required for process development
• Analytical method validation support, managing and processing samples, handling inventory of reagents and consumables and improvement projects
• Administrative tasks and ensuring laboratory Key Performance Indicators (KPIs) are met

Qualifications:

• Strong analytical skills attention to detail results-oriented approach. ability to strictly follow written and oral instructions, safety procedures, and GLP standards
• Proficiency in laboratory information management systems and other PC software applications like MS Office is crucial
• Strong problem-solving abilities, capable of investigating root causes and developing solutions for issues and deviations
• Excellent interpersonal and communication skills are vital for effective collaboration with internal teams and external stakeholders
• Prior experience as a lab analyst in the biochemical or medical sector, or in Quality Control, is beneficial
• Experience with at least one of the following is a must: UPLC-HPLC (pref. on Empower platform)/capillary gel electrophoresis/ELISA