Promotional Regulatory Affairs Specialist – Europe (Barcelona, Spain)Alcon is a global eye‑care leader that values inclusion and innovation.

We seek a specialist to manage the review of promotional and advertising assets across Europe, ensuring alignment with regulatory requirements and internal compliance.

Responsibilities- Manage promotional and advertising asset projects across Spain, France, the Nordics, and the UK/Ireland, ensuring documents are reviewed, routed, and finalized through the integral process.- Review promotional, marketing, medical, and scientific materials for compliance risks such as unsupported claims, off‑label promotion, and label misalignment.- Lead MAP meetings and collaborate with Marketing, Medical, Legal, Regulatory, Franchise, and Commercial stakeholders to support decisions and prevent Assist regional teams in Spain, France, the Nordics, and the UK/Ireland, applying written English, French, and Spanish proficiency to review documents and support local commercial efforts.- Drive process adoption and continuous improvement for promotional review workflows, maintaining documentation discipline and compliance with SOPs, GxP expectations, and regulatory standards.

Qualifications- Bachelor’s degree in Life Sciences,



Regulatory Affairs, Pharmacy, Communications, Marketing, Business, or a related field (equivalent experience considered).- Minimum four years of experience in regulatory affairs, promotional/advertising review, medical/legal/regulatory review, compliance operations, medical writing, or a similar Life Sciences environment.- Knowledge of European regulatory market requirements and experience supporting cross‑functional regional stakeholders.- Fluency in Spanish, French, and English; proficiency in Portuguese is a plus.- Strong attention to detail, regulatory judgment, stakeholder management, collaboration, accountability, and an ability to identify compliant alternatives that move the business forward.

Preferred- Experience with Veeva, Promo

Mats, MAP or MLR workflows, quality/process/project management, process improvement, SOPs, and GxP.- Knowledge of ophthalmology or ophthalmic products.

Benefits- Work in a collaborative, international environment with exposure to cross‑functional teams.- Access to a comprehensive benefits package, ongoing training, and continuous development opportunities.#J-18808-Ljbffr

📌 Promotional Regulatory Affairs Specialist, Europe (España)
🏢 Alcon Mx
📍 España