Promotional Regulatory Affairs Specialist, LATAM

• • Bachelor’s degree in Life Sciences, Regulatory Affairs, Pharmacy, Communications, Marketing, Business, or a related field; equivalent relevant experience may be considered.
• • Minimum 4 years of relevant experience in regulatory affairs, promotional/advertising review, medical/legal/regulatory review, compliance operations, regulated content workflows, medical writing, or a related Life Sciences environment.
• • Knowledge of LATAM regulatory market requirements and experience supporting cross-functional regional stakeholders; experience with Brazil-related asset review is highly valuable.
• • Spanish fluency, upper-intermediate to advanced English, and Portuguese sufficient to review written documents and promotional assets; spoken Portuguese is a plus.
• • Strong attention to detail, sound regulatory judgment, stakeholder management, collaboration, accountability, and the ability to find compliant alternatives that help the business move forward.
• • Preferred: experience with Veeva, PromoMats, MAP or MLR workflows, quality/process/project management, SOPs, GxP, ophthalmology, or ophthalmic products.
   

• • Join a new LATAM-focused role with the opportunity to bring the regional market into a global promotional review process and help shape how work gets done.
• • Work in a collaborative, international environment with exposure to Marketing, Medical, Legal, Regulatory, Commercial, and global stakeholders.
• • Access a comprehensive benefits package, ongoing training, and continuous development as part of a high-performing leader in ophthalmology.
   

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