GMP QC Analyst – Pharma Quality Assurance

Centrient Pharmaceuticals; Delft; On-site; EUR 42,000 - 54,000; Full time

Benefits offered by this job

34.5 days holidays

13th month (10%)

12 weeks parental leave

Laptop & cell phone

Performance bonus

Competitive pension

Job summary

Centrient Pharmaceuticals in Delft is seeking a QC Analyst to ensure the quality of raw materials, intermediates and enzymes in GMP-compliant analyses. You will support the QA laboratory, perform sample analysis, report results and investigate deviations, while maintaining documentation and equipment readiness.

The ideal candidate holds an MLO or HLO diploma and has at least 1 year of relevant experience. The role emphasizes accuracy, teamwork and the ability to handle high work pressure in a

Qualifications

• Minimum one year of experience in a similar QA role.
• Ability to work independently and accurately.
• Ability to work well in a team and under pressure.

Responsibilities

• Analyze raw materials, IPC, 7-ADCA and Enzymes samples per described methods.
• Report analytical results and investigate deviations.
• Maintain lab documentation, logs, SOPs and related FRM/WI.
• Prepare standards and buffer solutions and ensure equipment calibration.

Job description

Centrient Pharmaceuticals in Delft is seeking a QC Analyst to ensure the quality of raw materials, intermediates and enzymes in GMP-compliant analyses. You will support the QA laboratory, perform sample analysis, report results and investigate deviations, while maintaining documentation and equipment readiness.

The ideal candidate holds an MLO or HLO diploma and has at least 1 year of relevant experience. The role emphasizes accuracy, teamwork and the ability to handle high work pressure in a