Sr. QPPV Office (QPO) Specialist
BiomapasMaine, United States
Posted September 26, 2025
Full Time
About the Company
Biomapas is a functional and full outsourcing solution provider to the global life science industry. As a trusted partner for biopharmaceutical, medical device, cosmetics, and food supplement companies, we have one-stop-shop clinical research capabilities in high recruiting countries, delivering regulatory and pharmacovigilance excellence across Europe, CIS, MENA, and LATAM regions through the entire product lifecycle. Our in-house experience combined with a hands-on mindset allows for tailored solutions to complicated challenges that emerge on your path to commercialization. Our professionals execute your projects efficiently, cost-effectively and aspire to partner with you and become an integral part of your team from Early Development to Commercial success. We keep our promises. Always. Social media privacy policy: bit.ly/privacy-biomapas
Job Description
The Sr. QPPV Office (QPO) Specialist will focus on the development and oversight of pharmacovigilance systems and projects. This role involves ensuring compliance with regulations, representing the quality system, and collaborating with regulatory authorities. The position is located in Poland and requires a University degree in a Life Science field with at least 4 years of experience in pharmacovigilance.
Requirements
- University degree in Life Science field
- At least 4 years of experience in pharmacovigilance roles
- Expert knowledge of pharmacovigilance legislation
- Experience in regional QPPV role and risk minimization activities
- Experience in Pharmacovigilance Medical writing
- Strong computer literacy with intensive experience with safety databases
- Fluent English language
- Good knowledge of medical terminology
- Attention to detail, time-management and problem-solving skills
- Proficient knowledge in MS Office
- Ability to interpret and apply global drug safety regulations
- Good knowledge of medical terminology
- Fluent English language
- Good knowledge of medical terminology
- Attention to detail, time-management and problem-solving skills
- Proficient knowledge in MS Office
- Ability to interpret and apply global drug safety regulations
- Good knowledge of medical terminology
Benefits
- 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