Job Description The Local Country Person Responsible for Pharmacovigilance and Regulatory Affairs (LCPPV/LCPRA) serves as the primary local representative to ensure compliance with national pharmacovigilance and regulatory requirements. This dual-role position is responsible for executing PV and RA activities at the local level, supporting the Marketing Authorisation Holder (MAH) in maintaining product compliance throughout its lifecycle. Main responsibilities Primary contact person with local regulatory authorities for Regulatory Affairs and Pharmacovigilance as per local requirements Prompt and effective communication with local regulatory authorities Provision of local regulatory intelligence screening and expert advice Collection and reporting of locally suspected ADRs or ICSRs (FUs, translations) Local management / oversight of risk minimization measures related to urgent safety restrictions and emerging safety issues Preparation and collection of documentation for submissions to the regulatory authorities Review and linguistic input on local Product Information and Mock-ups Development and implementation of local pharmacovigilance system in compliance with Global MAH's system and local regulations Perform local non-indexed literature screening and screening of regulatory authority website/s for potential Adverse Drug Reactions (ADRs) and safety information Maintain accurate records and documentation at local level Provide support to the RA & PV Global operations team Ensure compliance with MAH's and PrimeVigilance's procedures Support audits and Inspections Handle local QA tasks such as suspected falsified products, quality alerts received from health authorities and other quality-related requirements received from the local market