QC Analyst, Biotech Lab (HPLC/UHPLC, GMP)

Akkodis

Waals-Brabant

On-site

EUR 55,000 - 75,000

Full time

14 days+
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Benefits offered by this job

Permanent contract
13.92 months salary
Company car or mobility budget
Flexible cafeteria plan
Hospitalization insurance
Training and development
Structured onboarding
Career discussions with manager
Community exchange
Referral bonuses
Cross-project opportunities

Job summary

Akkodis is seeking a Quality Control Analyst to join our biotech-focused laboratory team in Belgium. You will perform daily lab activities related to release and stability testing, analyse results, and verify data within a LIMS.

The scope covers HPLC/UHPLC and capillary electrophoresis, supporting GMP QC activities and collaborating with other analysts to organize analyses. Candidates have a Bachelor’s or Master’s in biochemistry or analytical chemistry, at least 5 years in biotech, strong

Qualifications

  • Bachelor’s or Master’s degree in biochemistry or analytical chemistry
  • At least 5 years of equivalent experience in biotech
  • GMP standards in QC laboratory
  • Good interpersonal, verbal, and written communication skills
  • Fluent in English (reading scientific documents)

Responsibilities

  • Perform daily laboratory activities related to release and stability testing
  • Analyse results
  • Verify data (double check)
  • Collaborate with other analysts to organize release and stability analyses
  • Follow up deviations and incidents and validate results within a LIMS system

Skills

Laboratory skills
Quality skills
English proficiency

Education

Bachelor’s or Master’s degree in biochemistry or analytical chemistry

Tools

HPLC/UHPLC
Capillary electrophoresis (CGE/iCE)

Job description

Akkodis is seeking a Quality Control Analyst to join our biotech-focused laboratory team in Belgium. You will perform daily lab activities related to release and stability testing, analyse results, and verify data within a LIMS.

The scope covers HPLC/UHPLC and capillary electrophoresis, supporting GMP QC activities and collaborating with other analysts to organize analyses. Candidates have a Bachelor’s or Master’s in biochemistry or analytical chemistry, at least 5 years in biotech, strong

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