PAre you ready to join a strongworld leader /strong in the exciting and dynamic fields of thestrong Pharmaceutical and Medical Device industries? PQE Group /strong has been at the forefront of these industries strongsince 1998 /strong, with strong40 subsidiaries /strong and more than strong2000 employees in Europe, Asia and the Americas. /strong /ppbr/ppWe are currently seeking a dedicated and motivated strongQuality Control Quality Assurance Specialist /strong to support a major pharmaceutical project focused on strongquality control /strong and strongquality assurance /strong activities within a GxP-regulated environment. /ppThe consultant will work onsite in Madrid until February, directly involved in operational and documentation-related tasks, and will then continue in hybrid mode from our headquarters or remotely. /ppbr/pp❗ strongPlease note: /strong strongFull onsite until February 2026 /strong for this project's duration; stronghybrid mode /strong following that (remote and/or from our main office) /ppbr/ppuResponsibilities include, but are not limited to: /u /pulliExecute, review, and coordinate all strongquality control activities /strong related to the strongmicrobiological qualification of classified areas /strong. /liliSupport stronganalytical method validation /strong, including drafting and reviewing related protocols and reports. /liliMaintain, update, and review strongGxP documentation /strong to ensure full compliance with applicable regulations and internal standards. /liliProvide support for strongutilities qualification /strong and other system qualification activities. /liliContribute to the strongimplementation and validation of computerized systems /strong within the ongoing project. /liliCollaborate with technical and QA teams to ensure full alignment with established quality procedures. /li /ulpbr/ppuRequired Qualifications: /u /pulliDegree in strongPharmacy, Chemistry, Biotechnology, Engineering /strong, or related scientific disciplines. /liliMinimum of strong2 years of experience /strong in strongQuality Control, Quality Assurance, or Validation /strong roles within the strongpharmaceutical or biotech industry /strong. /liliStrong knowledge of strongGMP/GxP regulations /strong and qualification/validation guidelines. /liliProven ability to manage, review, and write technical documentation in a regulated environment. /liliExcellent organizational and communication skills. /lilistrongFluent Spanish /strong and good command of strongtechnical English /strong are required. /li /ulpbr/ppstrongNext Steps /strong /ppUpon receiving your application, if a match is found, the Recruiting department will contact you for an initial HR interview. /ppIf there's a positive match, a technical interview with the Hiring Manager will be arranged. /ppIn the case of a positive outcome coming from Hiring Manager interview, recruiter will contact you for further steps or to discuss our proposal. /ppAlternatively, if the outcome is negative, we will contact you to halt the recruitment process. /ppbr/ppstrongWorking at PQE Group /strong /ppAs a member of the PQE team, you will be part of a strongchallenging, multicultural company that values collaboration and innovation /strong. PQE Group gives you the opportunity to work on international projects, improve your skills and interact with colleagues from all corners of the world. /ppIf you are looking for a rewarding and exciting career, PQE Group is the perfect place for you. /ppApply now and take the first step towards an amazing future with us. /p