ppAre you ready to join a bworld leader /b in the exciting and dynamic fields of the bPharmaceutical and Medical Device industries? PQE Group /b has been at the forefront of these industries bsince 1998 /b, with b40 subsidiaries /b and more than b2000 employees in Europe, Asia and the Americas. /b /ppWe are currently seeking an experienced bCommissioning, Qualification Validation (CQV) Consultant /b in bBarcelona /b. This role will focus on the qualification and validation of equipment and systems in biotechnological production facilities. /ph3Responsibilities /h3ulliExecute bcommissioning, qualification, and validation activities /b for pharmaceutical/biotech equipment and systems /liliPrepare, review, and execute bCQ and validation documentation (URS, DQ, IQ, OQ, PQ protocols, test scripts, and summary reports) /b /liliCollaborate with cross‑functional teams b(Engineering, QA, Validation, Manufacturing) /b to ensure compliance with bGMP, regulatory guidelines, and project timelines /b /liliReview btechnical documentation, PIDs, FAT/SAT protocols,



and vendor manuals /b /liliIdentify, troubleshoot, and document deviations, ensuring timely resolution /liliEnsure all activities meet bGMP, FDA, EMA, and ICH requirements /b /liliProvide project updates and progress reports to stakeholder /li /ulh3Required Qualifications /h3ulliBachelor’s degree in Engineering, Life Sciences, or related field /lilibAt least 2 years of experience /b in IQ/OQ/PQ protocol development and execution and CQ for pharmaceutical/biotech facilities, including construction of production plants /liliStrong knowledge of GMP, FDA, and EU regulations /liliExcellent analytical, problem‑solving, and communication skills /liliAbility to work independently and collaboratively in a project environment. /lilibSpanish native, English fluent (at least B2) /b /lilibSalary starts from 30.000€ gross per year /b /li /ul /p #J-18808-Ljbffr

📌 CQV Consultant (Barcelona)
🏢 Pqe Group
📍 Barcelona