Life Sciences Job at ProductLife Group, Romania | Pharmacovigilance Officer | Apply Now
If you are an experienced drug safety professional or a life sciences graduate looking to take full operational ownership of localized safety reporting, this position at ProductLife Group (PLG) is an exceptional opportunity. Located in Bucharest, Romania, this role positions you as the primary regulatory anchor for all regional pharmacovigilance operations. For detail-oriented specialists searching for a high-impact Life Sciences job, this position offers total ownership of adverse event tracking, local literature reviews, and audit readiness. It serves as an elite operational launchpad for a long-term Pharmacovigilance Job and stands out as a premier choices for professionals looking to secure an advanced corporate Job in Romania within a top-tier international life sciences firm.
- Job Position: Pharmacovigilance Officer
- Location: Bucharest, Bucharest, Romania
About The Company
ProductLife Group (PLG) is a highly respected, global life sciences outsourcing and consulting partner dedicated to helping pharmaceutical, biotech, and cosmetic companies safely navigate complex regulatory landscapes. Headquartered in Paris, France, the group operates an expansive international network across North America, Europe, and the Asia-Pacific (APAC) region, delivering expert services in regulatory affairs, quality assurance, and comprehensive drug safety management.
Life Sciences Job – Key Responsibilities
The Local Pharmacovigilance Officer assumes full, end-to-end responsibility for executing and safeguarding all regional pharmacovigilance (PV) operations in strict alignment with Good Pharmacovigilance Practices (GVP).
Your primary tracking, regulatory compliance, and client liaison duties include:
- Adverse Event & PV Reporting: Collecting, documenting, evaluating, and processing localized pharmacovigilance reports and adverse events, ensuring accurate entry into international safety databases.
- Inquiry Management: Hosting and managing local safety calls, addressing incoming drug safety questions, and drafting formal technical replies for regional stakeholders.
- Regulatory Intelligence Analysis: Monitoring, analyzing, and reporting on changing local safety guidelines, decrees, and legislative shifts across Romania to ensure continuous product compliance.
- Local Literature Support: Conducting regular, systematic screenings of localized medical and scientific literature to identify, flag, and log potential unlisted adverse drug reactions to advance this Life Sciences job.
- Direct Client Coordination: Acting as the primary operational point of contact for pharmaceutical clients, capturing specific business conventions, and aligning day-to-day operations with their strategic needs.
- Audit & Inspection Readiness: Participating actively in internal quality audits and external health authority inspections, preparing documentation packages to protect this Pharmacovigilance Job environment.
- Cross-Functional Training: Designing and delivering training modules for other client team members to ensure total institutional alignment regarding safety reporting protocols.
Qualifications & Profile Requirements For Life Sciences Job
ProductLife Group seeks an independent, highly organized life scientist who exhibits exceptional emotional intelligence and the cross-functional capability to communicate complex medical concepts with absolute clarity.
- Required Academic & Experience Criteria:
- Educational Foundation: A formal University degree in a relevant Life Science discipline to support this Job in Romania.
- Professional Track Record: A minimum of 1 to 2 years of direct experience operating within a pharmacovigilance department for service providers (CROs) or pharmaceutical operating companies.
- Linguistic Mastery: Absolute native or professional proficiency in the Romanian language is mandatory for reviewing local literature and handling regulatory texts, paired with strong English communication skills.
- Technical Skills & Competencies:
- Complete, functional understanding of European Union pharmacovigilance directives, local Romanian regulations, and international GVP guidelines related to medicinal or cosmetic safety.
- Practical, hands-on experience navigating specialized Safety Databases (e.g., Argus, ArisGlobal, or similar tracking software).
- High proficiency across the Microsoft Office Suite (Word, Excel, PowerPoint) for documenting compliance metrics.
- Strong analytical capabilities, excellent organizational habits, and the professional agility to deliver constructive feedback to matrixed teams.
In short, the Pharmacovigilance Officer position at ProductLife Group is a definitive route to transitioning your pharmaceutical or life sciences degree into a highly sought-after drug safety asset. Securing this appointment allows you to move past secondary administrative processing and take autonomous charge of the literature screenings, safety database workflows, and regulatory filings that protect patient health across Europe. If you reside in Bucharest, possess a pharmacy or science background, and meet the 1-2 year pharmacovigilance threshold, apply today to secure this premier Life Sciences job, launch a highly rewarding Pharmacovigilance Job, and lock in this outstanding corporate Job in Romania.
