Job Description The Pharmacovigilance Specialist is responsible for ensuring adherence to all applicable regulations, company policies and procedures. The Specialist, PV may be designated by the PV lead to serve as the Back-up (BU) local Qualified Person for PV (QPPV) / BU Local PV Contact / BU Local Responsible PV person as required per local PV legislation. When designated, in the absence of the PV Lead, they may manage day-to-day PV activities and serve as their back-up with supervision by a higher-level manager, as required. Requirements: *Education: Chemicals, Pharmaceutical chemist - 2+ years of experience in Pharmacovigilance *Knowledge in Adverse Events, Pharmacovigilance regulations, follow-up with patients. *Knowledge in Excel, Power BI. *English - Advanced level Activities: 1. Responsible for execution of local PV processes and activities in collaboration with applicable internal functional areas and external parties, ensuring alignment with local legislation and local/regional/global company procedures and policies. Activities may include but are not limited to management and negotiation of local PV agreements, local due diligence activities, Post approval Safety Monitoring Program (PSMP) implementation, scheduling and coordinating aggregate safety report submissions, conducting local training, review of local initiatives for compliance with PV requirements, communication of safety issues. 2. Responsible for day-to-day adverse events case management which may include case intake, translations (English and/or local language (as applicable)), acknowledgments, follow-up and submission activities in accordance with PV procedures and country regulations. 3. Supports local PV, business partner and vendor audits and inspections including readiness activities, document requests and CAPA activities. 4. Participates in issue management/compliance activities and coordinates / prepares the necessary local corrective actions. 5. Supports development and maintenance of local PV procedures and controlled documents in compliance with local, regional and global standards, to ensure global quality PV data. 6. Supports PV self-inspections as required by PV Legislations (where applicable). 7. May be assigned responsibility for ensuring appropriate implementation and oversight of Risk Minimization Measures and Additional Risk Minimization Measures locally as per department policy and local legislations. 8. Prepare/maintain/submit local RMPs to the local HA (as applicable). 9. May be responsible for managing and performing local literature screening and assessment in accordance with company procedure and local requirements (as applicable). 10. Support local implementation of applicable business continuity plans 11. Responsible for filing, storage and archiving of safety-related documentation in accordance with company policies and local requirements. 12. Serves as local Subject Matter Expert on relevant PV regulations, processes, and procedures. 13. Translates or QCs translation of applicable PV documents. 14. Supports PV Lead in maintaining the local PV Training matrix and onboarding plans. 15. May be responsible for reviewing, providing input and approving local initiatives (e.g., digital interfaces, marketing initiatives/ patient programs, organized data collection systems, etc.), and other programs to ensure compliance with PV requirements, as applicable 16. May be responsible for Health Authority Website Monitoring for potential safety issues, safety alerts, and new/revised PV requirements in compliance with company procedures and local legislation (as applicable). 17. Liaises with the local business units to keep them apprised of safety activities and provides input on strategic decisions. 18. Represents PV in cross-functional organizational and alliance partner forums as needed. 19. Participates on local company committees and councils for matters impacting PV as assigned. 20. Participates in special projects or rotational assignments within or outside of IPV as part of their professional development. 21. Responsible for completing all required/applicable trainings assigned at time of hire and after hire, by the due dates and before performing the activity. Current Employees apply Current Contingent Workers apply Search Firm Representatives Please Read Carefully Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails. Employee Status: Project Temps (Fixed Term) Relocation: VISA Sponsorship: Travel Requirements: Flexible Work Arrangements: Hybrid Shift: Valid Driving License: Hazardous Material(s): Required Skills: Adaptability, Adverse Event Report, Applied Engineering, Clinical Trial Management, Communication, Complaint Management, Compliance Investigations, Data Analysis, Data Management, Detail-Oriented, Drug Safety Surveillance, Employee Training, Management Process, Pharmacovigilance, Regulatory Communications, Regulatory Compliance, Risk Management, Veterinary Products Preferred Skills: Job Posting End Date: 08/15/2025 *A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.