Regulatory Affairs Manager - Pharma/Medical Device

Industry:                                Lifescience Industry: Pharma, Medtech, Digital Health Employment Type:                   Full-time Job Functions:                         Regulatory Affairs Location:                                 Meditrial, Via Po 9 Rome, Italy Workplace:                              Office-based / availability to travel  The Regulatory Affairs Manager (Pharma)  oversees the regulation process for products (Medical Device and Marketing Authorization)  requiring governmental approval, including filing necessary applications and handling all government interactions.
The Position will ultimately support and/or drive strategic regulatory strategies for multiple projects together with the subject matter experts.
Coordinates inspections of the organization and contract facilities, and develops procedures to ensure regulatory compliance pre and post-market.
The position is office-based (Rome)   Responsibilities • Management of a CTD (Electronic Common Technical Document) • Collaborate during implementations of regulatory strategies for New MA through National/Decentralized/Centralized Procedures • Preparing the submissions of variations type I, II, Renewals, and Safety variations • Manage the CMC activities (updating module III of ECTD) • Collaborate during the Management of Recall • Collaborate during the Technical File (TF) creation and any updates • Relationship with manufacturer • Interface with all pharmaceuticals database • Review and submission of promotional materials • Support the management of clinical investigations • Manage the Medical Device Post-marketing and Surveillance Medical Devices activities • Notify the new Food Supplements and any changes to Ministry of Health • Supervise International Regulatory and Quality activities • In addition to the above activities, the role can be asked to carry out tasks related to the belonging function or that may result from business needs Qualification Education: Master's Degree in science or related field, Doctor of Medicine MD is a plus; Thorough experience in life-science field and Regulatory Affairs; Languages: proficiency in oral and written English and Italian (third language is a plus); Proficient in Microsoft Office (MS Outlook, MS Word, MS Excel, Ms Power Point); Excellent communication, planning and organizational skills; Demonstrated ability to handle multiple competing priorities.