Promotional Regulatory Affairs Specialist, Europe

• 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 European regulatory market requirements and experience supporting cross-functional regional stakeholders
• Spanish fluency, French Fluency and English Fluency, (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, process improvement, SOPs, GxP,
• Nice to have knowledge of ophthalmology, or ophthalmic products.
   

• Join a new Europe-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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