ppAt Perrigo, we are driven by our mission to Makes Lives Better Through Trusted Health and Wellness Solutions, Accessible to All. We are proud to be a Top 10 player in the European Consumer Self-Care market and the largest U.S. store brand provider of over the counter and infant formula. Dedicated to providing The Best Self-Care for Everyone, we are the people behind the brands you trust. We are Opill®, Compeed®, Solpadeine®, NiQuitin®, and many more. We Are Perrigo. We are committed to enhancing the wellbeing of our colleagues and consumers alike. We pride ourselves on fostering an inclusive, collaborative culture where each person can experience a sense of belonging. /p h3Description Overview /h3 pIn this role you will support Category Innovation Growth projects by delivering defined regulatory activities for Cosmetic products and either Medical Device/Medicines products. /p h3Scope of the Role /h3 pYou will Support regulatory strategy development and perform regulatory activities in support of integral innovation and growth projects for assigned portfolio and/or projects in a specific Category. /p h3Key Responsibilities /h3 ul liProvide regulatory input to new product development, geo-expansion and existing product innovation for assigned product portfolio. /li liContribute to regulatory strategy development for innovation projects for all markets in scope (gathering and drafting requirements, identifying pathways to market and supportable claims). /li liPrepare technical documentation components for submissions, PIFs and labelling in line with document management processes. /li liSupport master label and artwork development and claims review. /li liSupport registration/notification procedures for certification of new products and may communicate with Notified Bodies and regulatory authorities as needed.



/li liResponsible for managing central Cosmetic Product Notifications. /li liSupport due diligence activities and gap analysis assessments. /li liSupport smooth handover/transition to LCM following initial launch. /li liBuild regulatory knowledge via regulatory intelligence, training and networking. /li /ul h3Experience Required /h3 ul liBachelor’s Degree in Life Sciences or relevant scientific/technical discipline. /li liMinimum 3 years in Regulatory Affairs – position dependant on experience. /li liExpertise in Cosmetic Product Regulation and a demonstrated practical experience of regulatory affairs for medical device or medicines products within consumer healthcare or self-care in EU, US or other markets. /li liFluent in English. /li /ul h3Benefits /h3 pWe believe our people are our greatest asset. Alongside competitive compensation, we offer benefits tailored to supporting you and your family, as well as career development opportunities to ensure you feel valued and supported, both professionally and personally. /p pFind out more about Total Rewards at Perrigo. /p h3Hybrid Working Approach /h3 pWe love our offices and the setting they provide for in-person collaboration and celebration. But we also appreciate the opportunity to work remotely can energise you too, so we promote flexibility with the ability to work two days a week from home in many roles. /p pWe are proud to be included in the Forbes list of "America's Best Employers by State 2024". Find out more. /p pWe are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or other characteristics protected by law. #weareperrigo /p /p #J-18808-Ljbffr

📌 Regulatory Affairs Strategist (San Cugat del Vallés)
🏢 Perrigo Company
📍 San Cugat del Vallés