Validation Specialist – Sterilization Processes

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.

Responsibilities:

-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.

Requirements:

-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.

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

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