Analyst Quality Control

Position: Analyst – Quality Control

Location: Bilthoven, Netherlands

Domain: Pharmaceuticals / Biotechnology / Clinical Research

Experience: 1–2 years

Employment Type: Full-time

Citizenship / Visa: European Citizens only (already based in the Netherlands preferred)

Job Purpose: The Analyst – Quality Control will be responsible for conducting analytical testing, documentation, and compliance activities within the Quality function. The role ensures that finished product (FP) analysis meets regulatory and organisational standards, while supporting continuous improvement and operational excellence.

Key Accountabilities:

I. Analytical Testing

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  Analyse assigned samples using validated procedures and calibrated instruments.

  
  


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  Conduct instrumental analysis independently (HPLC with Chromeleon 6.8 / 7.2).

  
  


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  Perform FP release analysis as per commitment dates without errors.

  
  


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  Check, review, and evaluate test results against set specifications.

  
  


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  Ensure compliance with GLP and good documentation practices.

  
  

II. Compliance & Reporting

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  Follow all approved SOPs, specifications, and GMP requirements.

  
  


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  Prepare analytical reports, CoAs, audit reports, and method transfer documentation.

  
  


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  Ensure proper sampling, preparation, and execution of analyses in line with safety norms.

  
  

III. Documentation & Records

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  Complete all documentation online using approved templates.

  
  


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  Maintain accuracy, integrity, and authenticity of records.

  
  


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  Prepare and update documents as per GMP requirements.

  
  

IV. Laboratory Maintenance

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  Maintain a clean, compliant, and safe working environment.

  
  


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  Dispose of samples and solutions as per SOPs.

  
  


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  Support calibration, qualification, and validation activities.

  
  


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  Draft/review SOPs and maintain lab equipment.

  
  

V. Continuous Improvement

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  Provide suggestions for cost-saving, process simplification, and automation.

  
  


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  Participate in operational studies and improvement projects.

  
  

Major Challenges:

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  Ensuring timely release of FP samples.

  
  


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  Managing deviations, non-conformances, and instrument breakdowns.

  
  


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  Balancing compliance with operational efficiency.

  
  

Key Interactions:

Internal: QA, Lab Planning, Lab Assistants.

External: Service Engineers (for instrument-related issues).

Skills & Knowledge:

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  Education: B.Sc. / M.Sc. / B.Pharm (Chemistry).

  
  


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  Experience: 1–2 years in pharmaceutical QC.

  
  
  
  
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    Preferred: 1 year in MDI / DPI / Nasal / Respiratory formulations.

    
    
  
  
  
  


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  Language: English (required).

Additional Information:

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  Reports to: Head QA/QC.

  
  


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  Interviews: 2–3 rounds.

Application Process:

To apply, please submit your CV and a cover letter detailing your relevant experience and qualifications for the role. Applications will be reviewed on a rolling basis, so early submissions are encouraged.

Equal Opportunity Employer:

We value diversity and are committed to creating an inclusive work environment. We encourage applicants from all backgrounds to apply.

Contact: Elvis Eckardt