More jobs:
Sr. QPPV Office; QPO Specialist
Job in
Town of Poland, Jamestown, Chautauqua County, New York, 14701, USA
Listed on 2026-02-04
Listing for:
Biomapas
Full Time
position Listed on 2026-02-04
Job specializations:
-
Healthcare
Pharmacy Technician, Pharmacy
Job Description & How to Apply Below
Location: Town of Poland
Join our global Pharmacovigilance team as a Sr. QPPV Office (QPO) Specialist.
Sr. QPPV Office (QPO) Specialist is responsible for the development of pharmacovigilance systems, and the oversight of end-to-end pharmacovigilance activities and projects' compliance with Quality Management System as well as the reporting and exchanging of safety and pharmacovigilance information for medicinal products.
Position is in any EU country.
Responsibilities- Manage full Pharmacovigilance systems and projects (or part of them)
- Promote, maintain, improve compliance with Pharmacovigilance (PV) tasks and responsibilities
- May act as Regional QPPV or deputy
- Influence the performance of the quality system and PV activities
- Develop, update, and review standard operating procedures for global pharmacovigilance processes, and implement changes to fulfill requirements
- Supervise, prepare and submit PSURs, Risk Management Plans and risk minimization activities
- Be the primary point of contact for PV-related matter; ensure oversight of the contractual partner safety data exchange agreements
- Ensure the survey and monitoring of European (including UK) level pharmacovigilance regulations
- Provide Pharmacovigilance trainings
- Ensure continuous safety profile monitoring, detection of new signals and evaluation
- Communication with Competent Authorities
- Participate in related inspection and/or audits
- University degree in Life Science field
- At least 4 years of experience in pharmacovigilance roles, including in-depth, demonstrated experience in most areas pertaining to pharmacovigilance, and expert knowledge of pharmacovigilance legislation
- Experience in regional QPPV role and risk minimization activities will be considered as an asset
- Experience in Pharmacovigilance Medical writing
- Strong computer literacy with intensive experience with safety databases
- Ability to interpret and apply global drug safety regulations
- Fluent English language
- Good knowledge of medical terminology
- Attention to detail, time-management and problem-solving skills
- Proficient knowledge in MS Office
- Professional growth and career opportunities
- International team and environment
- Bonus based on annual performance
- Personal accident and business trip insurance
- Influenza vaccines
- Rewarding referral policy
- Workplace establishment allowance
- Flexible working hours
- Team building, global meetings, B active events
To View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
Search for further Jobs Here:
×