Cleaning Validation Engineer

Are you ready for the next step in your career? As a technical specialist in the Life Science sector, you work on technologies that improve lives. You play a key role in the development and optimization of systems for drug production, medical devices and biotechnology, for example.

Your work is crucial to the success of these projects.

Responsibilities

• As a Cleaning Validation you are responsible for the timely validation of cleaning processes within a biopharmaceutical manufacturing environment.
• You perform cleaning validation activities for a wide range of CIP/COP processes on biopharmaceutical processing equipment.
• You execute hands-on validation activities.
• You prepare, review, and maintain cleaning validation protocols and reports.
• You plan and schedule cleaning validation activities in alignment with production schedules.
• You support and coordinate physical testing activities related to cleaning validation.
• You provide expertise and support troubleshooting activities in collaboration with Manufacturing and QA.
• You work as part of the broader QA Validation organization and ensure effective cross-functional communication with relevant departments.

Requirements

• Relevant scientific or technical degree, or equivalent experience.
• Experience in a GMP-regulated pharmaceutical or biotechnology manufacturing environment.
• Knowledge of cleaning validation and CIP/COP processes.
• Familiarity with EU and US GMP regulations (e.g. EudraLex, ICH, 21 CFR, EU Annex 1).
• Strong quality and safety mindset with good organizational skills.
• Ability to work independently and collaboratively in cross-functional teams.
• Basic proficiency with standard computer applications (e.g. MS Word, Excel).
• Strong communication skills in English and Dutch.

At STAR, your career is our focus. We connect you with challenging projects, offer personal guidance and create opportunities with clients you are excited about.

Together we make sure you get the most out of your career.