EHS Advisor (Pharma)
Pubblicato il 08-09-2026 - ACS DOBFAR in Roma
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. almeno 1 anno di esperienza in Pharmacovigilance laurea in discipline scientifiche (preferibilmente Farmacia o CTF) ottime capacità organizzative, attenzione al dettaglio e attitudine al problem solvingLa posizione rappresenta un'interessante opportunità di crescita qualificato in un ambiente dinamico e strutturato, con coinvolgimento in attività di case management, screening della letteratura, signal detection, reportistica aggregata e processi di qualità.
La posizione è full-time presso gli uffici di Agrate Brianza con possibilità di 10 giorni di smart working al mese.
Role: Drug Safety OfficerReports to: Drug Safety ManagerMain responsibilities: Ensures that all activities are performed in compliance with applicable pharmacovigilance guidelines and procedures. Conducts screening of spontaneous adverse event reports in EudraVigilance. Performs literature searches using PubMed, MLM, and local scientific journals.
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 EudraVigilance Medicinal Product Dictionary (XEVMPD).Assists Drug Safety Specialists in the preparation of aggregate reports (PADERs and PSURs).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 guidelinesFamiliarity with the EudraVigilance system, with the ability to support the entry and management of safety reports under supervisionGood knowledge of the MedDRA dictionary and its use for coding adverse event dataUnderstanding of fundamental pharmacovigilance principles and key international regulatory requirementsSoft Skills Required: Problem-solving skills with a proactive and solution-oriented approachAbility to work independently, with appropriate levels of supervision for a junior roleStrong attention to detail and accuracy in performing tasksEffective interpersonal and communication skills, with the ability to collaborate within the Drug Safety Unit and Regulatory Affairs departmentAbility to manage multiple activities simultaneously while respecting deadlines and prioritizing workload effectivelyIT Skills Required: Proficiency in Microsoft Office tools (Word, Excel, PowerPoint)Proficiency in Adobe AcrobatLanguage 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 TechnologyPrevious 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.)