Process & Cleaning Validation Specialist Ii

:Evaluate manufacturing process documents and equipment cleaning procedures for validation purposesDevelop protocols and conduct process validation for product manufacturing and aseptic filling (Media fill)Perform cleaning validation of cleaning procedures and ensure periodic cleaning verificationManage validation protocols for cleaning, process, and Media FillCollaborate with other departments to define protocol contents and actions to be carried outValidate manufacturing processes, cleaning procedures, and APS/Media FillSupport the drafting and approval of documents for new product transfer and validationHandle deviations related to validation activitiesEnsure accurate execution of validation activities and detailed analysis of resultsDraft validation reports and ensure proper archiving of all documentationProvide quality support for new product transfer and process qualificationActively participate in the design, construction, and implementation of new processes or manufacturing departmentsRequirements:Bachelor's Degree or equivalent in a scientific/pharmaceutical area2 years of previous related experience in the pharmaceutical sectorKnowledge of pharmaceutical techniques, production, and aseptic filling processesExperience in risk management and client service/project managementProficiency in Microsoft Office softwareFluent in English with advanced written and oral communication skills