Sanofi Group Pharmacovigilance Quality Documentation and Training Associate - VIE Contract (W/M) in Bridgewater, New Jersey

#LI-DNI

iMove, the Sanofi VIE Program, is available to citizens of the European Economic Area (EU + Norway, Liechtenstein and Iceland) aged between 18 and 28.

PLEASE NOTE that since this program is primarily an international development program, candidates cannot apply to a VIE assignment in their own country of citizenship.

PLEASE NOTE that applications that are only submitted in French cannot be considered by our non-French speaking partners at Sanofi worldwide.

Therefore, only applications that are submitted in English will be considered.

At Sanofi diversity and inclusion is foundational to how we operate and is embedded in our Core Values. We respect the diversity of our people, their backgrounds and experiences. We recognize to truly tap into the richness diversity brings we must lead with inclusion and have a workplace where those differences can thrive and be leveraged to empower the lives of our employees, patients and customers.

We are looking for a candidate for a VIE mission of:

Pharmacovigilance Quality Documentation and Training Associate - VIE Contract (W/M)

Responsabilities:

  • Contributing to the development and maintenance of the Pharmacovigilance Quality system

  • Supporting the Global Pharmacovigilance (GPV) quality documentation (QD) and its related training

  • Contributing QDs e-learning modules development for distribution to the pharmacovigilance network

  • Supporting the activities linked to the Electronic Data Management System (EDMS)

  • Supporting the activities linked to the company Learning Management System (LMS)

  • Promoting harmonization of quality standards

  • Contributing to the preparation of metrics and Key Performance Indicators

  • Supporting GxP (good practice) inspections and audits impacting PV training and quality documentation activities

  • Participating to specific projects related to PV (Pharmacovigilance) or quality process or tools improvements

  • Ensuring that customer requests are answered on due time

Candidate:

  • Master Degree in Pharmacy (BS, RPh, Pharm D) or Nursing or Biological Science discipline (Biology, Health Sciences…)

  • 1-2 years of experience in pharmacovigilance or quality

  • Excellent communication skills (oral and written)

  • Excellent organizational and planning capabilities

  • Ability to work in transversal/cross functional teams

  • Excellent teamwork and interpersonal skills

  • Ability to take initiative and to overcome challenges

  • Capability to work under pressure

  • Knowledge of International (ICH - International Conference on Harmonisation/CIOMS - The Council for International Organizations of Medical Sciences), EU (Good PV practices) and FDA (Food and Drug Administration) regulations in the domain of Pharmacovigilance.

  • Knowledge of electronic data management system would be a plus

  • English fluent

Sanofi is dedicated to supporting people through their health challenges. We are a global biopharmaceutical company focused on human health. We prevent illness with vaccines, provide innovative treatments to fight pain and ease suffering. We stand by the few who suffer from rare diseases and the millions with long-term chronic conditions.

With more than 100,000 people in 100 countries, Sanofi is transforming scientific innovation into healthcare solutions around the globe.

Sanofi, Empowering Life

Sanofi is dedicated to supporting people through their health challenges. We are a global biopharmaceutical company focused on human health. We prevent illness with vaccines, provide innovative treatments to fight pain and ease suffering. We stand by the few who suffer from rare diseases and the millions with long-term chronic conditions.

With more than 100,000 people in 100 countries, Sanofi is transforming scientific innovation into healthcare solutions around the globe.

Sanofi, Empowering Life