Work Type: 1-Year Direct Contract (with possibility of extension / permanent) | Onsite – Bilthoven, Netherlands

Experience: 3–5 Years (Pharma QC, including 2–3 years in Respiratory formulations)

Compensation: EUR €30,000 – €40,000 annually + 10% Variable

Benefits: Relocation Assistance Provided | Contract Extension / Conversion Possible

Notice Period: 0–30 Days

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Job Overview

• We are seeking a Senior Executive QC Analyst with experience in pharmaceutical quality control (Respiratory dosage forms – MDI/DPI/Nasal). The role involves performing sampling, analytical testing of finished products, instrument calibration, documentation, and compliance with GMP/GLP standards. The candidate will ensure timely release of finished products, accurate reporting, and contribute to process improvements within the QC lab.
  
  

Key Responsibilities

• Perform analysis of finished product (FP) samples using validated procedures and calibrated instruments.
• Independently operate and manage HPLC systems (Chromeleon software v6.8 & 7.2).
• Review and evaluate test results against specifications before release.
• Prepare and review Quality Reports, Certificates of Analysis (CoA), Analytical Method Transfer reports.
• Ensure compliance with Good Laboratory Practices (GLP), Good Manufacturing Practices (GMP), and safety norms.
• Document all activities in approved formats/templates (LIMS, online entries).
• Maintain laboratory hygiene, equipment calibration, qualification, and validation schedules.
• Support audits, inspections, and preparation of SOPs.
• Suggest process improvements and contribute to automation initiatives for efficiency.
  
  

Must-Have Skills

• Educational Background: B.Sc. / M.Sc. (Chemistry) / B.Pharm.
• 3–5 years of QC experience in pharmaceutical organizations.
• 2–3 years in respiratory formulations (MDI/DPI/Nasal).
• Strong knowledge of HPLC operations, GLP/GMP documentation, and LIMS systems.
• English language proficiency (written & spoken).
• Candidates must be based in the Netherlands or hold valid EU work authorization.
  
  

Nice-to-Have Skills

• Experience in analytical method validation & transfer.
• Familiarity with regulatory audits and compliance inspections.
• Exposure to cost-saving & process improvement projects.
  
  

Candidate Requirements

• EU Citizenship / Valid Work Permit for the Netherlands.
• Willingness to work onsite in Bilthoven.
• Availability to join within 0–30 days.
• Flexibility for 2–3 rounds of interviews (virtual & in-person).
• 394. 27541 - Senior Verification Engineer