Pharmacovigilance Audit and Inspection Readiness Manager at Sanofi in Bridgewater, New Jersey

Job Description:

Job title: Pharmacovigilance Audit and Inspection Readiness Manager



Location: Bridgewater, NJ



About the Job



We deliver 4.3 billion healthcare solutions to people every year, thanks to the flawless planning and meticulous eye for detail of our Manufacturing & Supply teams. With your talent and ambition, we can do even more to protect people from infectious diseases and bring hope to patients and their families.



Main Responsibilities:



Reporting to the Medical/PV Audit and Inspection Readiness Head, the PV Audit and Inspection Readiness (AIR) Manager is responsible to ensure:

• Participation in the ongoing permanent inspection preparedness and readiness of Global Pharmacovigilance (Patient Safety Pharmacovigilance-PSPV)PSPV), Medical GBUs and country PV offices in anticipation of regulatory inspections and audits.
  
  


• Active involvement in the preparation, conduct and follow-up of GxP regulatory inspections impacting PV/Medical until closure.
  
  


• Active involvement in the organization of appropriate support for the preparation, conduct and follow-up of Global Quality audits impacting country GxP activities, global PV and Medical processes/tools, Global PV vendors or Business Partner PV audits, until closure.
  
  


• Follow-up of audit/inspections PV/Medical-related Corrective and Preventive Actions (CAPAs) to ensure timely completion and coordination of CAPA effectiveness reviews in collaboration with CAPA owners, as needed to prevent recurrence.
  
  


• Management of Business Partners PV Audits activity, in collaboration with external auditors and related PSPV.
  
  


• Support in external relations with Inspectorates / Agencies / Pharma associations / Inter-Company network to ensure surveillance of PV inspections regulations/practices and benchmark on recurrent PV findings.
  
  


• Support completion of Health Authorities and Business partners pharmacovigilance risk assessment questionnaires to facilitate risk-based PV inspection planning
  
  

About you:

• Bachelor's degree Pharmacy (BS, RPh, Pharm D) or nursing (BSN, BScN) or biological science discipline. Advanced degree preferred.
  
  


• 7+ years of experience in global pharmaceutical industry, including experience in both post-marketing and clinical development activities.
  
  

• 5+ years of experience in Pharmacovigilance or clinical field, preferably in quality management activities.
  
  


• Experience working in a global environment, across diverse cultures.
  
  

Soft Skill & Technical Skills: Strong communication, problem solving, and leadership skills



Languages: English required, Spanish a plus



Why choose us?

• This role provides the opportunity to work at the forefront of digital innovation in the pharmaceutical industry.
  
  

• Bring the miracles of science to life alongside a supportive, future-focused team.
  
  


• Discover endless opportunities to grow your talent and drive your career, whether it's through a promotion or lateral move, at home or internationally.
  
  


• Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.
  
  


• Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks' gender-neutral parental leave.
  
  

#GD-SG
#LI-GZ
#LI-Onsite
#vhd Apply Now