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Associate Scientist – MSAT Pharmaceutical Process Development

Job in 2300, Leiden, South Holland, Netherlands
Listing for: SIRE LIFE SCIENCES
Full Time position
Listed on 2026-06-19
Job specializations:
  • Pharmaceutical
    Pharmaceutical Manufacturing, Pharmaceutical Science/ Research, Quality Engineering, Validation Engineer
Salary/Wage Range or Industry Benchmark: 40000 - 60000 EUR Yearly EUR 40000.00 60000.00 YEAR
Job Description & How to Apply Below

Company

We are a global healthcare organisation focused on innovation in manufacturing science and technology. In this role, you’ll support cross‑functional teams to develop and deliver technology and science projects that strengthen product performance, reliability, compliance, and efficiency across the end‑to‑end product life cycle.

Role Description

Support MSAT and Emerging Technologies projects focused on pharmaceutical manufacturing, new product introductions, process improvements, technology transfer, and advanced manufacturing initiatives. Work with cross‑functional teams to improve product quality, manufacturing efficiency, compliance, and cost performance.

Key Responsibilities
  • Support new product introductions (NPI) and technology transfer activities.
  • Provide technical support for formulations, manufacturing processes, and analytical methods.
  • Assist with process development, process characterization, and manufacturing improvements.
  • Support quality, compliance, and cost reduction (COGS) initiatives.
  • Conduct feasibility studies, troubleshooting, and data analysis.
  • Collaborate with MSAT, Manufacturing, R&D, and external manufacturing sites.
Requirements
  • Education - BS in Chemistry, Pharmaceutics, Chemical Engineering, Pharmaceutical Sciences, Materials Science, or related field.
  • Experience - 1-2 years of experience in pharmaceutical, biotech, MSAT, process development, analytical development, or formulation development.
  • Technical Skills
    • Material characterization (spectroscopy, microscopy, thermal analysis).
    • Analytical chemistry and analytical methods.
    • GMP/cGMP environment.
    • Basic understanding of QbD, PAT, validation, and pharmaceutical manufacturing processes.
    • Statistical analysis and Minitab exposure preferred.
  • Tools - Minitab, SharePoint/Document Management Systems and MVA Software.
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Position Requirements
10+ Years work experience
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