PACS DOBFAR S.p.A., multinazionale italiana, leader nella produzione di API e Prodotti Finiti, è alla ricerca di un un/una candidato/a motivato/a per un percorso di tirocinio universitario o post-laurea nell’ambito della microbiologia farmaceutica e dei processi asettici. La risorsa sarà coinvolta in attività chiave legate al controllo della contaminazione, alla qualità e alla compliance regolatoria, collaborando attivamente con team multidisciplinari in un contesto altamente regolato. /ppbrPer una comprensione completa di questa opportunità e dei requisiti per essere un candidato di successo, continui a leggere.br/ppIl ruolo offre l’occasione di acquisire esperienza pratica nella gestione delle deviazioni, nel monitoraggio ambientale e dei processi, nonché nella qualificazione e ottimizzazione dei processi asettici. Il/la tirocinante contribuirà inoltre a progetti di validazione, miglioramento tecnologico e assurance della sterilità, supportando al contempo attività di training e audit. /ppbr/ppCerchiamo una persona con solide basi scientifiche, forte attenzione al dettaglio e interesse per il settore farmaceutico, desiderosa di sviluppare competenze tecniche e trasversali in un ambiente dinamico e orientato alla qualità. /ppbr/ppstrongMain responsibilities: /strong /polliEnsure the management of deviations within the assigned scope, evaluating the criticality of processes and products, supporting batch disposition activities, responding to notifications and tasks, and aligning with Quality Operations on corrective and preventive actions. /liliCollaborate with the coordinator in defining the site Contamination Control Strategy key elements, like qualification and requalification activities of aseptic processes: sterilization, environmental monitoring, disinfection of environments, and study of process conditions including airflow visualization. /liliCollaborate with the coordinator in the evaluation and implementation of new microbiological analytical methods. /liliAssess environmental (viable non-viable), personnel and utilities monitoring data. /liliPerform production oversight to ensure the correct execution of aseptic techniques and processes. /liliSupport the delivery of training to staff on Microbiology, Pharmaceutical Hygiene and aseptic techniques. /liliParticipate in project teams related to validation, compliance and technological improvement, with focus on sterility assurance and microbiological laboratory qualification activities. /liliParticipate in working groups for the definition of rules and procedures in the context of aseptic production. /liliAssess decontamination, sterilization and depyrogenation data for compliance. xdwybme /liliSupport activities during regulatory authorities and customer audits. /li /olpbr/ppstrongTechnical/Regulatory Skills Required: /strong /polliBasic knowledge of cGMP regulations /liliBasic knowledge of aseptic processes and aseptic techniques /liliBasic knowledge of microbiology /liliGood experience in technical writing /li /olpbr/ppstrongSoft Skills Required: /strong /polliEffective communication and collaboration abilities across departments and hierarchical levels /liliGood problem-solving and decision-making skills /liliGood teamwork skills /li /olpbr/ppstrongIT Skills Required: /strong /polliProficiency in managing email using Outlook /liliGood knowledge of Microsoft Office (Word, Excel, PowerPoint, etc.) /li /olpbr/ppstrongLanguage Skills Required: /strong /polliItalian: Native or professional proficiency, written and spoken (C1) /liliEnglish: Professional proficiency, written and spoken (B2) /li /olpbr/ppstrongEducation: /strong /pulliChemistry and Pharmaceutical Technology or equivalent degree /li /ulpbr/ppstrongPrevious experience in the role or in a similar position within the sector: /strong /pulliNot necessary /li /ulpbr/ppstrongCertifications and Authorizations: /strong /pulliNot Applicable /li /ul