Full-time

Principal Process Validation Engineer

Posted by West Pharmaceutical Services • Eschweiler, North Rhine-Westphalia, Germany

📍 Eschweiler, North Rhine-Westphalia 🕒 March 02, 2026

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About the Role

Job Summary
In this role, you will be responsible for contributing to the development and implementation of the validation engineering strategy whilst ensuring the qualification and validation of equipment, facilities, utilities, automated systems, processes and process cleaning procedures are carried out in accordance to GMP and relevant guidelines.
Essential Duties and Responsibilities

Lead the validation effort for all Strategic Projects on site.
Lead the preparation, review, and approval of the Site Validation Master Plan.
Develop Validation Plans to support Site Validation Master Plan.
Site subject matter expert on Cleaning Validation, Process Validation, Equipment Validation, Computer System Validation, Data Integrity and Facility Qualification.
Preparation, review and or approval of qualification and/or validation documentation (specifications, protocols, reports etc.) in relation to instrument...
                

Job Details

Location Eschweiler, North Rhine-Westphalia
Job Type Full-time
Category Engineers
Posted March 02, 2026
Deadline April 11, 2026

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