Romania · Remote OK
Biomapas Group is looking for Senior Pharmacovigilance Specialists (Senior PVS) who will be responsible for an international pharmaceutical company for global operational delivery for assigned tasks on the project level.…
Skills: Pharmacovigilance, Audit Management, CAPA Management, KPI Management, PV Intelligence
Ukraine · Remote Solely
Biomapas Group is looking for Senior Pharmacovigilance Specialists (Senior PVS) who will be responsible for an international pharmaceutical company for global operational delivery for assigned tasks on the project level.…
Skills: Pharmacovigilance, CAPA Management, Audit Tracking, KPI Management, QMS
Greece · Remote OK
Join our Quality Assurance department as a Quality Assurance Manager. Quality Assurance Manager is responsible for supervision of quality management system within an organization, including its development, implementatio…
Skills: Quality Management System, GxP Auditing, SOP Development, Pharmacovigilance, Good Clinical Practice
Croatia · Remote OK
Join our Quality Assurance department as a Quality Assurance Manager. Quality Assurance Manager is responsible for supervision of quality management system within an organization, including its development, implementatio…
Skills: Quality Management System, GxP Auditing, SOP Development, Pharmacovigilance, Good Clinical Practice
Bulgaria · Remote OK
Join our Quality Assurance department as a Quality Assurance Manager. Quality Assurance Manager is responsible for supervision of quality management system within an organization, including its development, implementatio…
Skills: Quality Management System, GxP Auditing, SOP Development, Pharmacovigilance, Good Clinical Practice
Romania · Remote OK
Join our Quality Assurance department as a Quality Assurance Manager. Quality Assurance Manager is responsible for supervision of quality management system within an organization, including its development, implementatio…
Skills: Quality Management System, SOP Development, GxP Auditing, Pharmacovigilance, Good Clinical Practice
Poland · Remote OK
Join our Quality Assurance department as a Quality Assurance Manager. Quality Assurance Manager is responsible for supervision of quality management system within an organization, including its development, implementatio…
Skills: Quality Management System, GxP Auditing, SOP Development, Pharmacovigilance, Clinical Research
Lithuania · Remote OK
Join our Quality Assurance department as a Quality Assurance Manager. Quality Assurance Manager is responsible for supervision of quality management system within an organization, including its development, implementatio…
Skills: Quality Management System, GxP Auditing, SOP Development, Pharmacovigilance, Good Clinical Practice
Lithuania · Remote Solely
Join our global team as Clinical Lead. Clinical Lead is responsible for the clinical operations of a project within a defined regional/global level. Provides oversight of project deliverables, assigned Clinical Research …
Skills: Clinical Operations, Project Oversight, CRA Management, ICH-GCP Compliance, Monitoring Plan Development
Slovakia · Remote Solely
Join our global Pharmacovigilance team as a Medical/Clinical Safety Specialist. Medical/Clinical Safety Specialist is responsible for assuring compliance with the Quality Management System. Participating in the collectio…
Skills: Pharmacovigilance, Clinical Safety, ICSR Processing, MedDRA Coding, Regulatory Reporting
Czechia · Remote Solely
Join our global Pharmacovigilance team as a Medical/Clinical Safety Specialist. Medical/Clinical Safety Specialist is responsible for assuring compliance with the Quality Management System. Participating in the collectio…
Skills: Pharmacovigilance, Clinical Safety, ICSR Processing, MedDRA Coding, Veeva Vault Safety
Poland · Remote Solely
Join our global Pharmacovigilance team as a Medical/Clinical Safety Specialist. Medical/Clinical Safety Specialist is responsible for assuring compliance with the Quality Management System. Participating in the collectio…
Skills: Pharmacovigilance, Clinical Safety, ICSR Processing, MedDRA Coding, Safety Database Management
Bulgaria · Remote Solely
Join our global Pharmacovigilance team as a Medical/Clinical Safety Specialist. Medical/Clinical Safety Specialist is responsible for assuring compliance with the Quality Management System. Participating in the collectio…
Skills: Pharmacovigilance, Clinical Safety, ICSR Processing, MedDRA Coding, Regulatory Reporting
Croatia · Remote Solely
Join our global Pharmacovigilance team as a Medical/Clinical Safety Specialist. Medical/Clinical Safety Specialist is responsible for assuring compliance with the Quality Management System. Participating in the collectio…
Skills: Pharmacovigilance, Clinical Safety, ICSR Processing, MedDRA Coding, Regulatory Reporting
Hungary · Remote Solely
Join our global Pharmacovigilance team as a Medical/Clinical Safety Specialist. Medical/Clinical Safety Specialist is responsible for assuring compliance with the Quality Management System. Participating in the collectio…
Skills: Pharmacovigilance, Clinical Safety, ICSR Processing, MedDRA Coding, Regulatory Reporting
Lithuania · Remote Solely
$2k–$2k/mo
Join our global Pharmacovigilance team as a Pharmacovigilance Specialist in Lithuania. Pharmacovigilance Specialist is responsible for assuring compliance with local and regional Quality Management System and interact, e…
Skills: Pharmacovigilance, Compliance, Safety Information Processing, Medical Information Handling, Literature Review
Hungary · Remote Solely
Join our global team as a Pharmacovigilance Specialist (Japanese Speaking) (Remote/home based). You will be mainly responsible for conducting global and local literature screening and assuring compliance with local and r…
Skills: Pharmacovigilance, Literature Screening, Compliance, Safety Information, Quality Management System
Ireland · Remote Solely
Join our global team as a Pharmacovigilance Specialist (Japanese Speaking) (Remote/home based). You will be mainly responsible for conducting global and local literature screening and assuring compliance with local and r…
Skills: Literature Screening, Pharmacovigilance, Japanese Fluency, English Fluency, MS Office
Spain · Remote Solely
Join our global team as a Pharmacovigilance Specialist (Japanese Speaking) (Remote/home based). You will be mainly responsible for conducting global and local literature screening and assuring compliance with local and r…
Skills: Literature Screening, Pharmacovigilance, Japanese Fluency, English Fluency, MS Office
Netherlands · Remote Solely
Join our global team as a Pharmacovigilance Specialist (Japanese Speaking) (Remote/home based). You will be mainly responsible for conducting global and local literature screening and assuring compliance with local and r…
Skills: Pharmacovigilance, Literature Screening, Compliance, Safety Information, Quality Management System
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The role involves operational and administrative coordination of Pharmacovigilance audits, CAPA management, and KPI tracking for an international pharmaceutical company. Responsibilities include maintaining audit tracking files, managing workflows in the Global QMS, and coordinating deliverables from CAPA owners.
Candidates must have a Pharmacy degree or life science background with at least one year of Pharmacovigilance experience. Proficiency in English and strong analytical skills are required, while experience in audit and CAPA management is an advantage.
Biomapas Group is looking for Senior Pharmacovigilance Specialists (Senior PVS) who will be responsible for an international pharmaceutical company for global operational delivery for assigned tasks on the project level. Senior PVS will act as the employee of international pharma company for the project. The person will report to Pharmacovigilance Manager of international company and there will be responsibilities under audit and CAPA management. This role provides operational and administrative coordination for Pharmacovigilance audit, CAPA, KPI management and PV Intelligence activities. Final quality assessment, CAPA approval, effectiveness review, and CAPA closure remain under the responsibility of the Quality Oversight team.
ResponsibilitiesA complete spectrum of Clinical Research, Regulatory Affairs, Pharmacovigilance and Medical Information solutions.
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
Offices: K. Donelaicio str. 60, Kaunas, LT – 44248, LT · 16 Pirogova, Almaty, 050040, KZ · 3 Route de la Corniche, Biopole, Lausanne, Epalinges 1066 , CH · Zemlyanoi val str., № 9, Moscow, Moscow City 105064, RU · Ilia Chavchavadze avenue, N 60b, floor 8, flat N 28, Tbilisi, - 0162, GE
A complete spectrum of Clinical Research, Regulatory Affairs, Pharmacovigilance and Medical Information solutions.
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
Offices: K. Donelaicio str. 60, Kaunas, LT – 44248, LT · 16 Pirogova, Almaty, 050040, KZ · 3 Route de la Corniche, Biopole, Lausanne, Epalinges 1066 , CH · Zemlyanoi val str., № 9, Moscow, Moscow City 105064, RU · Ilia Chavchavadze avenue, N 60b, floor 8, flat N 28, Tbilisi, - 0162, GE
