This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Regulatory Affairs and Patient Safety Talent Pool based in Brazil.

This opportunity is designed for experienced professionals in regulatory affairs and pharmacovigilance who are passionate about contributing to safer and more effective healthcare outcomes worldwide.
You will join a talent pool considered for multiple future roles across regulatory operations, labeling, safety, and compliance functions within global life sciences programs.
The scope spans diverse regulatory domains, including submissions, product labeling, safety monitoring, and interactions with health authorities.
You may be engaged in work that supports both strategic regulatory planning and operational execution across international markets.
The environment is highly collaborative and global, requiring close coordination with cross-functional clinical, regulatory, and safety teams.
This is an opportunity to apply your expertise to meaningful projects that directly impact patient safety and product quality.
You will contribute to advancing regulatory excellence and ensuring compliance across complex pharmaceutical development processes.

• Support regulatory affairs activities across multiple domains, including labeling operations, regulatory submissions, publishing, and compliance documentation.
• Contribute to regulatory strategy development for product labeling, advertising, promotion, and lifecycle management.
• Assist in Chemistry, Manufacturing, and Controls (CMC) activities, ensuring alignment with regulatory requirements and product quality standards.
• Participate in regulatory operations processes, including dossier preparation, submission tracking, and health authority interactions.
• Support patient safety activities, including monitoring, documenting, and analyzing safety events and adverse trends.
• Collaborate with global cross-functional teams to ensure compliance with international regulatory and pharmacovigilance standards.
• Ensure timely and accurate execution of regulatory and safety deliverables in alignment with global project requirements.

• Experience in Regulatory Affairs, Pharmacovigilance, or Patient Safety within the pharmaceutical or life sciences industry.
• Strong understanding of regulatory frameworks, submission processes, and/or safety reporting requirements.
• Knowledge of labeling, regulatory operations, CMC, or health authority interactions is highly valued depending on specialization.
• Familiarity with global regulatory environments and compliance standards.
• Strong analytical skills with attention to detail and ability to interpret complex regulatory information.
• Excellent communication and collaboration skills in a global, cross-functional environment.
• Ability to work independently in remote or hybrid environments while managing multiple priorities.
• Bachelor’s degree in life sciences, pharmacy, medicine, or related field preferred.

• Opportunity to be considered for multiple global regulatory and patient safety roles
• Remote-friendly opportunities depending on assignment
• Exposure to international regulatory frameworks and global healthcare projects
• Career development within regulatory affairs and pharmacovigilance functions
• Collaborative and mission-driven environment focused on improving patient outcomes
• Participation in high-impact pharmaceutical development programs
• Competitive compensation aligned with experience and role placement