Logo

Please Verify You're Human

Person

Jeisson Lopes

Assuntos regulatórios | industri...

Slough, United Kingdom

Nolea, linkedin, talent search
Profile Privacy
Jeisson's email
Engage via Email--
Jeisson's phone number
Engage via Phone --
Description

My professional journey in the pharmaceutical industry began after obtaining a solid education in biochemical pharmacy from the Fundação Educacional de Fernandópolis (FEF), followed by a postgraduate degree in Regulatory Affairs from the Institute of Science, Technology, and Quality (ICTQ). At Drogal Pharmacy Store, I worked as a Pharmacist Sub-manager, carrying out activities related to pharmaceutical care, sales, team management, and inventory control, adhering to principles such as Good Dispensing Practices. Upon joining EMS, a renowned pharmaceutical company, I joined the Quality Assurance department, focusing on Production Process Validation. In this role, I had the opportunity to oversee the production chain of medications and various pharmaceutical forms, including tablets, capsules, syrups, ointments, creams, eye drops, and oncology products, applying validation protocols according to guidelines set by regulatory bodies. Following the completion of my postgraduate studies, I transitioned to the Regulatory Affairs department at EMS, specifically to the Post-Marketing sector for pharmaceuticals. Here, I managed changes of both high and low complexity, including alterations in manufacturing site, formulation, packaging, and analytical methods, while ensuring compliance with regulations established by the regulatory authority ANVISA. I also monitored annual change histories and controlled alterations in leaflets and labelling as per regulatory requirements. At Eurofarma Pharmaceutical Industry, I began my international regulatory affairs career, working with the team to submit documents for drug registration in different Latin American countries, adhering to local laws and specific requirements of each country. Later, in the Post-Marketing team, I was responsible for managing changes and change control for the company's medications, including modifications to leaflets and labelling, renewal of Good Manufacturing Practice Certificates (GMP), and Operating Authorisations, ensuring the continuity of operations in compliance with national regulatory standards.

nmc

Profile Summary

Hire quickly, next hire, Nolea health

Your Next Hire Awaits!

Sign In to access millions of vetted professional health workers

Other members also viewed

instagram logo
X logo
linkedin logo
youtube logo