Ph3Experteer Overview /h3pAs Process Cleaning Specialist you will optimize and assure cleaning of production equipment to meet GMP and EMA/FDA expectations. You’ll work with manufacturing, QA and engineering to develop, validate, and monitor CIP/SIP and manual cleaning processes. You will draft and update technical docs, support deviation investigations, and contribute to cleaning validation and verification strategies. You’ll drive continuous improvement through trend analysis and support audits related to cleaning activities. This role sits at the heart of a site focused on sterile production within a global pharma leader, offering a meaningful, hands‑on impact. /ph3Retribuzione / Benefits /h3ulliManage and optimize cleaning processes for production equipment ensuring GMP compliance /liliCollaborate with manufacturing, QA and engineering to develop, validate and monitor cleaning processes (CIP/SIP and manual) /liliDraw up and update SOPs, validation protocols, and reports related to cleaning activities /liliSupport investigations into deviations or non-conformities in cleaning processes /liliParticipate in defining and implementing cleaning validation and verification strategies /liliContribute to continuous process improvement via trend analysis and CAPA /liliProvide support during internal and external audits regarding cleaning /li /ulh3Responsabilità /h3ulliDegree in Chemistry, Industrial Chemistry, Chemical Engineering, or related scientific disciplines /lili2–3 years of experience in a similar pharmaceutical/biotech role /liliIn-depth GMP knowledge and EMA/FDA cleaning validation guidelines /liliFamiliarity with analytical techniques to verify cleanliness (TOC, HPLC, visual residues) /liliDocument management and regulatory drafting skills /liliStrong analytical, problem-solving, and continuous improvement orientation /liliGood English proficiency; team-oriented and cross-functional collaboration /li /ul /p #J-18808-Ljbffr