Life Sciences Job at Recordati, France | Pharmacovigilance Data Analysis
If you are an experienced safety database analyst looking to apply your technical knowledge to global drug safety operations, this full-time position at Recordati is an exceptional opportunity. Located at the hub office in Puteaux, France, this on-site role embeds you directly within the core Pharmacovigilance Case Processing team. For detail-oriented data analysts searching for a high-impact Pharmacovigilance Job, this mid-senior position offers hands-on ownership of Argus database architecture, Individual Case Safety Report (ICSR) tracking, and cross-functional IT alignment. It serves as an elite launchpad for a long-term corporate trajectory and stands out as a premier Life Sciences Job for professionals seeking a rewarding Job in France.
- Job Position: Pharmacovigilance Data Analysis
- Job ID: 2644
- Location: Puteaux, FR
About The Company
Recordati is an international biopharmaceutical group with a century of history, dedicated to unlocking the full potential of life and keeping patients at the center of all discoveries. Operating across Europe, the Americas, Africa, and Asia, Recordati specializes in managing treatments for rare diseases alongside a robust consumer healthcare portfolio. The group’s culture is anchored by its core values: Better Together, Never Settle, and Always Deliver. Recordati proudly fosters an inclusive, equal-opportunity environment where employees are trusted, supported, and empowered to bring their whole selves to work.
Life Sciences Job – Key Responsibilities
As a PV Case Processing Associate, you will support the global pharmacovigilance department by managing safety data pipelines, streamlining automated workflows, and maintaining database configuration integrity.
Your day-to-day data, compliance, and operational duties will include:
- Argus Safety Operations: Executing day-to-day database administration tasks within Argus Safety, including product entries and clinical study tracking setups.
- Data Extraction & Analytics: Generating complex listings, aggregate data configurations, and custom safety reports directly from the database to advance this Pharmacovigilance Job.
- ICSR Workflow Monitoring: Managing the centralized pharmacovigilance mailboxes to ensure seamless collection, tracking, and reconciliation of incoming Individual Case Safety Reports (ICSRs).
- PV-IT Cross-Functional Bridge: Acting as the primary operational point of contact between global PV business units and IT teams to troubleshoot system integration bottlenecks.
- Audit & Inspection Readiness: Assisting with document preparation for regulatory health authority inspections, performing periodic Quality Control (QC) checks, and updating Standard Operating Procedures (SOPs) to secure a compliant Life Sciences Job.
- Vendor & Partner Liaison: Interacting daily with regional affiliates, external third-party service providers, and global partners to ensure absolute data consistency.
Qualifications & Profile Requirements For Life Sciences Job
This mid-senior vacancy is tailored for highly precise, rigorous data specialists who possess deep technical familiarity with standard pharmaceutical safety databases.
- Educational Foundation: A formal university Scientific Degree in Life Sciences, Biotechnology, or a related quantitative healthcare discipline.
- Industry Track Record: A minimum of 2 years of direct experience working in Pharmacovigilance (PV) operations or case processing units.
- Database Mastery: Proven, hands-on technical proficiency with the Argus Safety database platform, including tracking workflows and pulling database listings.
- Technical Competencies: Strong command of data management methodologies, automated data flows, and standard MS Office applications (specifically Advanced Excel).
- Linguistic Skills: Advanced written, spoken, and reading comprehension in English to operate efficiently within an international matrix environment.
- Core Behavioral Competencies:
- A collaborative mindset with a proven ability to work cross-functionally across different cultures.
- Strong organizational skills to manage competing case deadlines simultaneously.
- A proactive, solution-oriented approach with sharp attention to detail.
In short, the Pharmacovigilance Data Analysis role at Recordati is a definitive route to transitioning your technical database skills into a premium, corporate compliance asset. Securing this position allows you to step away from basic call-center data entry and actively manage the system configurations, data workflows, and quality control layers that guarantee international drug safety. If you are living in or willing to relocate to Puteaux, possess two years of verified Argus experience, and want to establish a career with a historic pharmaceutical leader, apply today to secure this premier Job in France.
