Process & Cleaning Validation Specialist
Are you ready to join a world leader in the exciting and dynamic fields of the Pharmaceutical and Medical Device industries?
We are seeking a Process & Cleaning Validation Specialist with solid experience in pharmaceutical validation activities. The consultants will be involved in validation lifecycle management, supporting both routine and project-related activities in a GMP-regulated environment.
Responsibilities
* Execute and coordinate process validation and cleaning validation activities according to GMP requirements.
* Support validation lifecycle activities from planning through execution and closure.
* Collaborate with Production, QA, QC, and Engineering departments to ensure timely project execution.
* Support investigations related to deviations, non-conformities, and change controls.
* Ensure compliance with internal quality standards and international regulatory expectations.
* Participate in continuous improvement initiatives related to manufacturing and validation processes.
Qualifications
* Proven experience in Process Validation and Cleaning Validation within the pharmaceutical or biotechnology industry.
* Experience working in manufacturing environments under strict quality standards.
* Strong technical writing and documentation skills.
* Fluent in English and Spanish.
PQE Group gives you the opportunity to work on international projects, improve your skills and interact with colleagues from all corners of the world.
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