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QC Analyst
Centrient Pharmaceuticals Netherlands · Delft, Netherlands
Performance bonusEntry

+10K new in the last hour

QC Analyst

Centrient Pharmaceuticals Netherlands · Posted Nov 6, 2026

Delft, South Holland, Netherlands
Entry
Performance bonus
1+ years

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Analyze samples according to GMP standards to ensure product quality.

Responsibilities

Analyse raw materials, intermediate and enzyme samples according to GMP standards
Report analytical results
Investigate deviations detected during analysis
Manage and archive department documentation
Determine final product status after analysis

Requirements

MLO or HLO diploma

Skills

GMP raw material analysis IPC documentation management lab equipment maintenance

Benefits

34.5 holidays
13th month bonus 10%
12 weeks gender neutral parental leave
Laptop & cell phone
Performance bonus

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