Sr Pharmacovigilance Analyst
Sr Pharmacovigilance Analyst
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Job Description
Com um legado nico em dermatologia e dcadas de inovao de ponta a Galderma a lder emergente na categoria de dermatologia presente em aproximadamente 90 pases. Oferecemos um portflio inovador baseado na cincia de marcas premium e servios que abrangem todo o espectro do mercado de dermatologia em rpido crescimento atravs de Esttica Injetvel Cuidados Dermatolgicos e Dermatologia Teraputica. Desde a nossa fundao em 1981 dedicamos nossa ateno e paixo ao maior rgo do corpo humano - a pele - atendendo s necessidades individuais de consumidores e pacientes com resultados superiores em parceria com profissionais de sade. Porque entendemos que a pele em que estamos molda nossas vidas estamos avanando na dermatologia para cada histria de pele.
Procuramos pessoas que se concentrem em obter resultados abracem a aprendizagem e tragam uma energia positiva. Eles devem combinar iniciativa com um senso de trabalho em equipe e colaborao. Acima de tudo devem estar apaixonados por fazer algo significativo para os consumidores pacientes e profissionais de sade que atendemos todos os dias. Nosso objetivo capacitar cada funcionrio e promover seu crescimento pessoal garantindo ao mesmo tempo que as necessidades comerciais sejam atendidas agora e no futuro. Em toda a nossa empresa abraamos a diversidade e respeitamos a dignidade a privacidade e os direitos pessoais de cada funcionrio.
Na Galderma damos ativamente s nossas equipes motivos para acreditar em nossa ousada ambio de nos tornarmos a principal empresa de dermatologia do a gente voc tem a oportunidade definitiva de adquirir novas e desafiadoras experincias de trabalho e criar um impacto direto incomparvel.
About Galderma
Galderma is the leading company in the category dedicated to dermatology present in approximately 90 countries. We provide an innovative science-based portfolio of premium brands and services that span the full spectrum of the rapidly growing dermatology market through Injectable Aesthetics Dermocosmetics and Therapeutic Dermatology. Since our founding in 1981 weve dedicated our focus and passion to the largest organ in the human body the skin meeting the individual needs of consumers and patients with superior outcomes in partnership with healthcare professionals. Were advancing dermatology for every skin story because we understand that the skin were in shapes our life stories.
Work at Galderma
At Galderma you will have the ultimate opportunity to gain life-changing work experiences. We are committed to meeting the individual needs of consumers and patients with superior outcomes in partnership with healthcare professionals.
At our company we embrace differences and respect diversity privacy and the personal rights of every employee. We are committed to keeping our workplace respectful and inclusive. We are proud of our dedication to diversity and inclusion and want to ensure that the people we do business with know share and respect our standards.
If you seek to put your ideas into practice make a difference and exercise your purpose your place is here.
Opportunity Main Responsibilities
What will you do:
Ensure quality management of all procedures implementation of the audit findings and Pharmacovigilance improvement projects in Latin America participating in the constant mapping of the implemented processes and review control of the documents and direct line of communication with the responsible by Pharmacovigilance of Europe (EU-QPPV) aiming the continuity of compliance with Latin America regulations local regional and international legislations and global pharmacovigilance policies.
Ensure that any request from the Health Authorities regarding safety information necessary to assess risk-benefit for Galderma products being available 24/7 in order to send complete answer and in accordance with regulatory deadlines in current legislation.
Operate the vigilance routine actions of Galderma Latin America post-marketing surveillance through review and submit to Global Pharmacovigilance (Corporate) the adverse event reports in order to ensure the compliance with national regional global legal and contractual rules.
Implement elaborate review and approve the procedures related to Latin America Pharmacovigilance and keep them updated through periodic search of pharmacovigilance regulations of Latin American and global procedures aiming the notifications quality of adverse events with Galderma products in accordance with current legislation and related good practice guides.
Review and ensure the implementation of pharmacovigilance training post-marketing Surveillance to all employees of Galderma Brazil Latin America LSOs and Regional PV Staff through periodic Pharmacovigilance actions according to the presential and conference call/web meeting scheduled trainings in order that all employees of Galderma America Latin be able to identify and report any adverse events related to Galderma products.
Elaborate and review the documentation for periodic Pharmacovigilance reports Pharmacovigilance Plan and Risk Minimization Plan when necessary in order to ensure the monitoring of Galderma products safety profile.
Notify and review the spontaneous reports of drug adverse events to all Health Authorities in Latin America with Galderma Affiliate through an electronic form on the regulatory agency website in order to comply the current legislation.
Ensure that all files related to the Pharmacovigilance and Customer Service areas will be manage following Good Practice of Pharmacovigilance through periodic and continuous document reviews in order to guarantee traceability according to the current legislation.
Participate in meetings with national entities public authorities organizations and associations of Pharmacovigilance and Customer Service aiming alignment with market actions and anticipation of regulatory and legal needs.
Elaborate and control of compliance metrics in Pharmacovigilance through KPIs management aiming the improvement of quality processes.
Support the execution of corporate audits at Galderma Affiliates in Latin America Countries and execute audits at Distributors under LATAM Regional responsibilities aiming ensure the Good Pharmacovigilance Practices.
Knowledge and Skills:
Strong verbal and written communication skills
Strong relationship problem-solving & negotiating skills.
Fluent in English and Spanish
Work Experience: Between 5 and 7 years in Pharmacovigilance
Conduct of Pharmacovigilance legislation Technovigilance NOTIVISA and CVS
Education:
- Professional education in the area of health with experience in Pharmacovigilance
Required Experience:
Senior IC
Employment Type
Full-Time
