Pharmacovigilance associate **ID**:1425 **Date of Posting**:Jun 14, 2025 **Business Area**:Pharmacovigilance **Job Type**:Direct Employee **On site / Remote / Hybrid**:Hybrid **Location**:Puteaux, FR **Territory**:
**Full-Time or Part-Time**:Tempo pieno **Seniority**:Entry level
- With its beginnings in a family run pharmacy in Correggio, Italy in the 1920s, Recordati is now a global pharmaceutical company, listed on the Italian stock exchange, with over 4,500 employees and turnover of over Euro 2bn._
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- We are a group of like-minded, passionate individuals who go to extraordinary lengths for our patients, customers, partners, investors and the people across the globe who we serve. We develop and commercialise medicines to serve people living with common diseases, as well as those living with some of the rarest, in around 150 countries._
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- At Recordati, our mantra is simple. We’ve always believed that health, and the opportunity to live life to the fullest, is a right, not a privilege. Whether that is for common diseases or the rarest - we want to give people the opportunity to be the best version of themselves._
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- This drive will never stop. Together, we will always be reimagining tomorrow - with new ideas, new technologies and new innovations to fight diseases._
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- Recordati. Unlocking the full potential of life._ **Job Purpose**
Corporate Pharmacovigilance Associate in the safety profile evaluation group / charge de pharmacovigilance surveillance du profil de securité- **Key Responsibilities**
- The pharmacovigilance associate is responsible for the assigned products with the support of a vendor
- medical assessement at case level
- literature review
- signal detection activities ( detection,



assessement, action takens ) / monitoring the implementation of CCDS change in the local product information
- Safety analysis authoring
- Answer to health authority questions during registration renewal...
- PBRER strategy coordinate the authoring
- RMP with associated risk minimization activities
- ensure process update with corresponding procedure for the assigned process
- participate to inspection and audits **Required Education**
Pharm D, Physician, Scientific profileMaster in pharmacovigilance or strong PV experience in the safety assessment profile> 2 years experience required in similar position**Required Skills and Experience**
organized, rigorus, accountable, committed,proactivity, synthetic mindset**Technical Competencies**
critical thinking,case analysis synthesis and case assessementmedical writing skillsproject managementSafety profile regulations and guidance knowledge#LI-KL1**Required Behaviours and Competencies**
accountabilityfocus on the targetteam spiritcreative and proactivityflexible**Required Languages**
fluent in english.**Travel required in %**
very few- At Recordati we believe in people! Inspired by our purpose - unlocking the full potential of life - we are committed to creating a diverse environment and cultivating a culture of inclusion. We strive to continually lead with our values and beliefs, enabling our employees to bring their whole selves to work and develop their potential._
- We are proud to be an equal opportunity employer. We recruit, develop and reward without regard to, amongst others, gender, sexual orientation, gender identity or expression, national origin, age, physical or mental ability, race, ethnicity, political or religious belief._

📌 Pharmacovigilance Associate (Provincia di Frosinone)
🏢 Recordati
📍 Provincia di Frosinone