Sterilization Validation Engineer
Job in
5830, Boxmeer, North Brabant, Netherlands
Listed on 2026-07-31
Listing for:
SIRE LIFE SCIENCES
Full Time
position Listed on 2026-07-31
Job specializations:
-
Pharmaceutical
Validation Engineer, Pharma Engineer, Pharmaceutical Manufacturing, Quality Engineering
Job Description & How to Apply Below
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 Overview
We are looking for an experienced Sterilization Validation Engineer 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.
Key Requirements
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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