Regulatory Affairs Analyst, Junior
Captativa
full-time
Posted on:
Location Type: Hybrid
Location: São Paulo • Brazil
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Job Level
About the role
- Prepare, review and update SOPs and other documents within the Quality Management System, ensuring compliance with national and international regulatory requirements;
- Responsible for transportation validation reports, ensuring that storage and distribution conditions maintain product integrity and quality;
- Support the management and control of regulatory documentation, audits, investigations of deviations and non-conformities, procedure training, and Good Manufacturing Practices.
Requirements
- Bachelor's degree in Pharmacy or a related field.
- Experience in regulatory affairs within the pharmaceutical industry.
- Fluent English, able to conduct meetings in English.
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
SOP preparationregulatory documentation managementtransportation validationauditinginvestigation of deviationsGood Manufacturing Practicesquality management system
Soft Skills
communicationmeeting facilitation
Certifications
Bachelor's degree in Pharmacy