Specialist Drug Safety (vet profile)
Location :
HybridType :
Full-timeThe QbD Group supports life sciences companies worldwide from idea to patient. QbD’s team offers knowledge & tailored (software) solutions in development, clinical, regulatory & compliance, production and distribution for companies active in ATMP, Biotech, Medical Devices, In Vitro Diagnostics, Digital Health and Pharma.QbD has affiliates in 8 different countries and can count on the expertise of more than 500 life science professionals and growing.What’s in it for you?
Make a real impact:
Contribute to shaping the future of the Life Sciences industry by supporting innovative projects and clients across pharma, biotech and medical devicesGrow within a community of experts:
Benefit from knowledge-sharing, mentoring, and exposure to diverse, challenging assignments that broaden your expertise.Build a meaningful career:
As an ambitious and pioneering company, we want to offer you the best possible environment to thrive within the life sciences.A fair, competitive package:
We offer tailored, transparent compensation aligned with your expertise, preferences, and local market regulations — because your contribution deserves to be valued.
What you’ll be doing:
Project Managing:
Acting as the primary contact point for project-related matters for the client and internally.Maintaining good client relations and ensuring a consistently high quality of work.Preparing project scope and objectives based on signed agreement between the client and QbD Group.Project activity planning, including meeting deadlines and interim milestonesReporting for the client and QbD Group management e.G. preparation of Monthly reports, serving as basis for invoicing.Develop and review Pharmacovigilance Standard Operating Procedures (SOPs/WI) for clients.Cases management controlData entry and quality control of PV cases in post-marketing and clinical trials, or related to medicinal products, medical devices and cosmetics.PV Assessment of any case of suspected adverse reaction.Direct contact with HCP and patients/consumers.Perform any follow-up activities required.Submission of cases to Eudravigilance, MHRA or any other Competent Authority.Perform bibliographic research in local scientific journals, international journals, MLM service and any other type of search.Management of medical information and answering queries.Review and control of Safety Regulatory intelligenceReview and control of Pharmacovigilance agreementsReview and control of Pharmacovigilance quality systemSupport in PV audits and inspections of clientsPharmacovigilance trainingPerform and manage PV metrics and KPIs linked to projects in charge.Participation in preparation of PV aggregate reports under supervision of Senior Drug Safety Officer)Client Support in Pharmacovigilance inspections and audits for services provided.Elaboration, follow-up and evaluation of the CAPA plan applicable to the project.Act as a Qualified Person Responsible for Pharmacovigilance on behalf of the different clients, at local level (Local-QPPV), acting as back-up (Deputy).What you bring
Required:
Bachelor's degree in Life Sciences or relatedMaster's degree in Pharmacovigilance, Pharmaceutical Industry or related. Desirable.High level of English. Must.Advanced informatic skills - knowledge of MS Office. Desirable.Experience in project management. DesirableKnowledge of Good European Pharmacovigilance Practices (GVPs)At least 2 years of experience in Pharmacovigilance, having been involved in:
cases management and signal detectionQuality knowledge regarding the management of deviations / CAPAs. DesirableKnowledge regarding Eudravigilance requirements for Marketing Authorization Holders (clients) and the processes with the Health Competent Authorities. Desirable.Experience in Pharmacovigilance audits. DesirablePersonal skills:
Good teamwork skills and high learning capacityParticipative and proactive in work groupsAttention to detailSkills and/or experience in the writing of scientific texts. DesirableOrganization ability and task prioritizationManagement of bibliographic research???? Who you are
Our culture is driven by values If this sounds like you, you’ll fit right in:
You’re
resilient
and tackle challenges with a positive mindsetYou’re
curious
and always up for learning something newYou have a
no non-sense approach
honest, clear, respectfulYou’re
innovative
and bring ideas, not just opinionsAnd above all, you’re
serious about your work, but not too serious about yourselfAbout us
We support life sciences companies from idea to patient — offering tailored solutions in development, clinical, regulatory, compliance, production, and distribution. With 500+ experts across 8 countries, we help drive innovation in ATMP, biotech, medical devices, diagnostics, digital health, and pharma.We believe in
JPEG :
Joy. Partnership. Going the Extra Mile. Getting Things Done.You won’t just be taking a job — you’ll be joining a community where people grow, laugh, build, and contribute to something bigger.Interested? Let’s talk.Send us your CV and motivation letter. You could be the next one to join the QbD family.
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