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Validation Analyst – III – Engineering-P3
Job in
5830, Boxmeer, North Brabant, Netherlands
Listed on 2026-07-23
Listing for:
SIRE LIFE SCIENCES
Full Time
position Listed on 2026-07-23
Job specializations:
-
Pharmaceutical
Pharmaceutical Manufacturing, Pharma Engineer, Quality Engineering, Regulatory Compliance Specialist -
Quality Assurance - QA/QC
Quality Engineering, Regulatory Compliance Specialist
Job Description & How to Apply Below
Validation Analyst III (Engineering, P3) About the Company
Our client is a global, research-driven pharmaceutical organization specializing in innovative medicines and vaccines. The Boxmeer site is one of the world's leading manufacturing and development locations for sterile veterinary vaccines, operating in a highly regulated GMP environment with a strong focus on quality, innovation, and continuous improvement.
Role OverviewWe are looking for an experienced Validation Analyst III to support a critical sterilization validation project. You will investigate, validate, and optimize filtration processes used in sterile manufacturing, ensuring compliance with GMP and regulatory standards.
Key Responsibilities- Lead sterilization and filtration validation activities.
- Develop and execute validation protocols, reports, and technical documentation.
- Investigate and improve filtration processes.
- Ensure GMP compliance throughout validation activities.
- Collaborate with Engineering, Manufacturing, and Quality teams.
- Bachelor's or Master's degree in Engineering, Chemistry, Life Sciences, or a related field.
- Minimum 5–6 years of pharmaceutical validation experience.
- Strong knowledge of GMP and validation documentation.
- Experience with filtration and sterilization processes.
- Understanding of aqueous and oil-based solution chemistry.
- Fluent in English.
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