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
Open Positions
QPO (QPPV office) Specialist
Bachelor's degree in Life Science. 2+ years pharmacovigilance experience. Knowledge of international regulations & PV databases
QPO (QPPV office) Specialist
BS degree in Life Science. 2+ yrs Pharmacovigilance experience. Knowledge of international regulations like ICH & EU GVP
Sr. QPPV Office (QPO) Specialist
Bachelor's degree in Life Science. 4+ years in pharmacovigilance experience. Expertise in pharmacovigilance legislation & compliance
Sr. QPPV Office (QPO) Specialist
Bachelor's degree in Life Science, 4+ years experience in pharmacovigilance. Experience with regional QPPV and risk minimization required. Expert knowledge of drug safety legislation and regulations is a must
QPO (QPPV office) Specialist
Bachelor's degree in Life Science. 2+ years of Pharmacovigilance experience. Knowledge of international regulations & experience with PV databases
QPO (QPPV office) Specialist
Bachelor’s degree in Life Sciences, 2+ years Pharmacovigilance experience, and knowledge of international regulations and databases. Strong computer skills and medical information experience preferred
Sr. QPPV Office (QPO) Specialist
Bachelor's degree in Life Science. 4+ years of experience in pharmacovigilance. Expert knowledge of pharmacovigilance legislation and regulations
QPO (QPPV office) Specialist
Bachelor's degree in Life Science. 2+ years experience in Pharmacovigilance. Knowledge of international regulations
Sr. QPPV Office (QPO) Specialist
Bachelor's degree in Life Science. 4+ years experience in pharmacovigilance. Knowledge of pharmacovigilance legislation and European drug safety regulations
Sr. QPPV Office (QPO) Specialist
Bachelor's in life science degree with 4+ yrs exp in pharmacovigilance & expertise in regulation. Strong computer skills & fluency in English are also required
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