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 Cleaning Validation Specialist to support cleaning validation activities within a GMP-regulated pharmaceutical manufacturing environment.
Responsibilities include, but are not limited to:Support the planning and execution of cleaning validation activities for manufacturing equipment and facilities.Participate in sampling activities and support analysis of validation data.Collaborate with Manufacturing, Quality Assurance, and Engineering teams to ensure compliance with GMP requirements .Support risk assessments and validation strategies related to equipment cleaning processes.Contribute to investigations, deviations, and CAPA actions associated with cleaning validation.Maintain and organize validation documentation according to regulatory and internal quality standards .Required Qualifications:Bachelor's or Master's degree in Pharmaceutical Sciences, Biotechnology, Chemistry, Chemical Engineering, or Life Sciences .Minimum 1 year of experience in the pharmaceutical, biotechnology, or related regulated industry (internships or academic projects are also considered).Basic understanding of GMP principles and pharmaceutical manufacturing environments.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.