Descrizione:
ACS DOBFAR S.p. A. multinazionale italiana leader nella produzione di API e Prodotti Finiti, è alla ricerca di una figura motivata e orientata alla qualità da inserire nel team di Pharmacovigilance come Drug Safety Officer. La risorsa sarà coinvolta in attività chiave legate alla gestione della sicurezza dei farmaci e alla compliance regolatoria, collaborando attivamente con team multidisciplinari in un contesto altamente regolato e internazionale. Il profilo ideale possiede: almeno 1 anno di esperienza in Pharmacovigilance buona conoscenza delle normative GVP, Eudra Vigilance e Med DRA laurea in discipline scientifiche (preferibilmente Farmacia o CTF) ottime capacità organizzative, attenzione al dettaglio e attitudine al problem solving La posizione rappresenta un'interessante opportunità di crescita professionale in un ambiente dinamico e strutturato, con coinvolgimento in attività di case management, screening della letteratura, signal detection, reportistica aggregata e processi di qualità. Se sei interessato/a o conosci qualcuno in linea con questa opportunità, inviaci la tua candidatura tramite questo annuncio o sul sito di ACS nella pagina "careers". La posizione è full-time presso gli uffici di Agrate Brianza con possibilità di 10 giorni di smart working al mese. Per questa selezione verranno considerati solo candidati/e domiciliati nelle vicinanze di Agrate Brianza. Role: Drug Safety Officer Reports to: Drug Safety Manager Main responsibilities: Ensures that all activities are performed in compliance with applicable pharmacovigilance guidelines and procedures. Conducts screening of spontaneous adverse event reports in Eudra Vigilance. Performs literature searches using Pub Med, MLM, and local scientific journals. Reviews and quality checks results from Eudra Vigilance and literature searches. Manages data entry of adverse event/adverse drug reaction (AE/ADR) reports in the pharmacovigilance database. Identifies, verifies, and confirms potential follow-up information and duplicate cases. Performs checks related to new referral procedures and PSUSA activities. Supports the preparation of product-related messages within the Extended Eudra Vigilance Medicinal Product Dictionary (XEVMPD). Assists Drug Safety Specialists in the preparation of aggregate reports (PADERs and PSURs). Supports Signal Detection Management activities. Manages electronic and paper archiving of pharmacovigilance documentation and reports. Contributes to Quality System activities, including deviations, CAPAs, changes, audits, and inspections. Ensures compliance with data integrity principles across all pharmacovigilance activities. Technical/Regulatory Skills Required: Good knowledge of pharmacovigilance regulations, including Good Pharmacovigilance Practices (GVP) and relevant Italian and European guidelines Familiarity with the Eudra Vigilance system, with the ability to support the entry and management of safety reports under supervision Good knowledge of the Med DRA dictionary and its use for coding adverse event data Understanding of fundamental pharmacovigilance principles and key international regulatory requirements Soft Skills Required: Problem-solving skills with a proactive and solution-oriented approach Ability to work independently, with appropriate levels of supervision for a junior role Strong attention to detail and accuracy in performing tasks Effective interpersonal and communication skills, with the ability to collaborate within the Drug Safety Unit and Regulatory Affairs department Ability to manage multiple activities simultaneously while respecting deadlines and prioritizing workload effectively IT Skills Required: Proficiency in Microsoft Office tools (Word, Excel, Power Point) Proficiency in Adobe Acrobat Language Skills Required: Italian: Native or professional proficiency both written and spoken (C1) English: Professional proficiency both written and spoken (B2) Education: Degree in scientific field, preferably Chemistry and Pharmaceutical Technology Previous experience in the role or in a similar position within the sector: At least 1 year of experience in the field of Pharmacovigilance. Certifications and Authorizations: Degree, preferably in a scientific field (Pharmaceutical Chemistry and Technology, Chemistry, Biotechnology, Biology, etc.)