Overview
Are you ready to join a world leader in the exciting and dynamic fields of the Pharmaceutical and Medical Device industries? We are currently seeking a dedicated and motivated Commissioning & Qualification (C&Q) Engineer to support facility, utility, equipment, and system qualification activities in Barcelona and Madrid. The role involves ensuring compliance with GMP requirements, company standards, and regulatory guidelines while contributing to the successful delivery of pharmaceutical projects. Responsibilities
Support commissioning and qualification activities for pharmaceutical facilities, utilities, and process equipment. Prepare and execute C&Q documentation (URS, DQ, IQ, OQ, PQ protocols, test scripts, and summary reports). Collaborate with cross‑functional teams (Engineering, QA, Validation, Manufacturing) to ensure compliance with project timelines and regulatory requirements. Participate in project meetings and provide updates on progress, risks, and mitigations. Qualifications
Bachelor’s degree in Engineering, Life Sciences, or a related field. Three or more years of experience in Commissioning & Qualification within the pharmaceutical or biotech industry. Fluent in English and Spanish (written and spoken). About PQE Group
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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