Validation Specialist – Sterilization Processes

Overview

Company Overview: A leading pharmaceutical organization focused on the production of sterile medicines. They operate state-of-the-art facilities and are committed to maintaining the highest standards of quality and safety in their products.

Job Description: We are seeking a skilled Validation Specialist to support the validation of sterilization processes. This is a project-based role based in Boxmeer, designed to ensure that filtration and sterilization methods meet strict industry standards. The successful candidate will play a vital part in investigating and optimizing filtration techniques to address current challenges with filter performance.

• Investigate existing filtration processes used during sterilization.
• Modify and improve filtration methods to ensure they meet sterilization requirements.
• Write validation protocols, reports, and statements to document findings and procedures.
• Collaborate with cross-functional teams on-site to implement process modifications.
• Ensure all activities comply with GMP guidelines and quality standards.
• Support validation activities from initial assessment through to final implementation.

• Minimum of 5–6 years of experience in the pharmaceutical sector.
• Proven experience in writing protocols, validation reports, and technical documentation.
• Strong knowledge of GMP regulations, sterilization, and filtration processes.
• Solid understanding of the chemistry of aqueous and oily solutions.
• Excellent communication skills in English; familiarity with Dutch is a plus but not required.

If you are interested and want to apply, please submit your application via the apply button below and contact me.