Promotional Regulatory Affairs Specialist, Europe
hace 2 días
Cornellà de Llobregat
Promotional Regulatory Affairs Specialist – Europe (Barcelona, Spain) Compruebe a continuación si tiene lo necesario para esta oportunidad y, si es así, envíe su solicitud lo antes posible. 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 global 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 escalations., • 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, PromoMats, 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. xcskxlj, • Access to a comprehensive benefits package, ongoing training, and continuous development opportunities. #J-18808-Ljbffr