Job Description
📋 Description Support local implementation of centrally authorized products with EMA coordination. Manage local lifecycle activities (variations, renewals, post-approval changes). Review translated product information texts and packaging for compliance. Collaborate on promotional/non-promotional materials for regulatory compliance. Maintain regulatory documentation and update internal systems. Support PV processes per global procedures and GVP. 🎯 Requirements Bachelor’s or Master’s in pharmacy, Life Sciences or related. 2–5 years of Regulatory Affairs experience in pharma. Experience with promotional material reviews is a plus. Fluent Italian and English (written and spoken). Proficiency in Microsoft Office. Master’s in Regulatory Affairs/Market Access is a plus. 🎁 Benefits Permanent, full-time contract. Health insurance for employee and family (Faschim). Annual welfare plan. Accident and life insurance policies. Short-term incentive plan. Professional development opportunities.
