VALIDATION SPECIALIST MILAN AND LATINA

ppbCSV Life Science Group /b, an international engineering company, market leader in the pharmaceutical sector, is looking for a bValidation Specialist to join its /bb CQV team in Milan and Latina offices. /bbr/The resource will be placed on a permanent contract. Grade level and salary will be commensurate with experience. /p h3REQUIRED ACTIVITY /h3 pWe are looking for a bValidation Specialist /b for our bMilan and Latina /b offices. The resource will join the CQV team and will be involved in structured projects for major players in the pharmaceutical industry. The resource will be responsible for drafting and executing qualification protocols in the field in accordance with predefined standards and ensuring compliance with relevant regulations. Specifically, she/he will perform the following activities: /p ul libDrafting, verification and execution of qualification protocols /b (DQ, IQ, OQ, PQ) for equipment, for equipment, facilities, and controlled contamination environments. /li liPerformingb thermal mapping /bstudies for temperature/humidity-controlled environments and equipment. /li libr/bInstrument calibration and verification /b activities. /li libDrafting and review of technical documentation: /bURS, VMP, Risk Assessment, GAP Analysis, PID. /li libQualification /bof HVAC systems, utilities (PW, WFI, Clean Steam), and process systems (RABS, isolators, autoclaves, freeze dryers). /li /ul pActivities will include interfacing with customers and suppliers, meeting and coordinating with multi-disciplinary project teams. /p h3REQUIRED CHARACTERISTICS /h3 pThe ideal candidate: /p ul liHas a Bachelor’s or Master’s degree in a bscientific discipline /b(engineering, chemistry, CTF or related). /li liIs familiar with the relevant regulations (EU GMP, FDA, Annex 11, GAMP5). /li liHas at least 3 years‘ experience in a similar role within the chemical-pharmaceutical sector. /li liHas a good knowledge of English (both written and spoken). /li liHas expertise in the validation of plants, equipment and processes in the chemical-pharmaceutical sector. /li liHe is familiar with the use of the main measuring instruments (multi-channel recorders, particle counters, anemometers, etc.). /li liHe is competent in CSV/Data Integrity. /li liHas excellent organisational, interpersonal and deadline management skills. /li /ul pbThis vacancy is open to candidates of all genders /b, in accordance with current legislation on equal treatment and non-discrimination (Legislative Decree 198/2006 and subsequent amendments). /p pAll applications will be assessed on the basis of skills, experience and potential, without discrimination on grounds of gender, gender identity or expression, sexual orientation, age, ethnic or national origin, religion or personal beliefs, marital status or disability. /p h3SEDE DI LAVORO /h3 pMilan and Latina. /p h3WHAT WE OFFER /h3 pIn CSV Life Science Group, you will find: /p ul liFull-time bpermanent contract /b and salary commensurate with experience. /li liTechnical and soft skills training (in the classroom and on the job). /li liOpportunities for bprofessional development and growth /bwithin the Group. /li liIntegration into a dynamic, innovative, and rapidly growing environment. /li liEmployee welfare benefits and company bbenefits /b. /li libSmart working /b and flexible hours compatible with field activities. /li /ul h3OUR CULTURE /h3 pInb CSV Life Science Group /b, you will have the opportunity to work on unique and challenging projects, collaborate with the best experts in the field and build a growing career. You will develop your skills and reach new professional milestones within an ever-expanding group of a thriving binternational organization /b that values byour growth and success. /b /p pWe promote bequal opportunity /b and are committed to a bdiverse and fair work environment. /b We believe that bvaluing diversity /bis the key to achieving great results and enriching our corporate culture. /p /p #J-18808-Ljbffr