Analista Documentação Técnica Regulatória Pleno (Sede: Itapevi/SP)
PfizerWhat You'll Do
Prepare and review documentation for product registrations and renewals for local and export products. Conduct evaluations related to post-registration changes and maintain compliance with regulatory requirements. Support during audits and inspections by regulatory bodies and ensure documentation is up-to-date.
What We're Looking For
Bachelor's degree in Pharmacy, Chemistry, or Chemical Engineering. 2 to 4 years of experience in Regulatory Affairs, Quality Assurance, or Quality Control. Advanced English proficiency and knowledge of pharmaceutical regulations.
Key Skills & Technologies
Additional Information
Experience Level
Mid-Level
Job Language
Portuguese
Employment Type
Full-time
Work Mode
On-site