Regulatory Affairs Manager, Se Lazio

Regulatory Affairs Manager, Se
Roma
Lazio, Lazio

Established in 1806 as a small soap and candle business in New York City, Colgate-Palmolive is now a truly global company with products sold in over 200 countries and territories under such internationally recognized brand names as Colgate, Palmolive, Softsoap, and many more. Colgate-Palmolive is a leading consumer products company that serves hundreds of millions of consumers worldwide with brands and products across four core businesses – Oral Care, Personal Care, Home Care, and Pet Nutrition.

We are committed to offering products that make lives healthier and more enjoyable. Job Title: Regulatory Affairs Manager, SETravel Required: 25% of timeHybridNo Relocation Assistance OfferedJob Number: 164255 - Roma, Lazio, ItalyWho We AreColgate-Palmolive Company operates in over 200 countries specializing in Oral Care, Personal Care, Home Care, Skin Care, and Pet Nutrition.

Join us in reimagining a healthier future for people, their pets, and our planet. The Regulatory Affairs function plays a crucial role in ensuring that Company's products comply with all relevant regulations; preparing, reviewing, and submitting regulatory documentation to local authorities; and advising on changes in regulatory legislation. The Regulatory Affairs Manager SE reports directly to the Senior Regulatory Affairs Manager.

The main responsibilities include:Stay abreast of the current and incoming European/National regulatory framework relevant to Colgate's portfolio, focusing on personal care cosmetic products. Represent Colgate's interests in local/EU Trade Associations and Consortia. Maintain key partners informed on evolving regulatory requirements relevant to Colgate's portfolio. Support expert regulatory assessments and ensure effective execution of regulatory strategies. Provide regulatory support on day-to-day issues and training to internal stakeholders. Write clear Regulatory Assessments and documents for stakeholders. Ensure regulatory compliance and maintenance of product registrations throughout the product life-cycle. Establish strong relationships within the European Division and with Global Partners. Provide assistance to authority inspections. Ensure the review and approval of artworks for products. Provide input for budget preparation and reviews. Collaborate in regional and global regulatory projects. Contribute to the effective use of the network of regulatory consultants. Requirements:Bachelor or Master's in science, pharmacy, medicine, or law.

Preferred: Advanced degree (PhD, PharmD). A minimum of 4-5 years in regulatory affairs and/or regulatory intelligence. Languages: Fluent in Italian and English; knowledge of Spanish, Portuguese, or Greek is a plus. Excellent working knowledge of the European markets and regulators. Ability to analyze new regulations and assess their impact. Ability to work collaboratively across different businesses and cultures. Strong organizational skills and attention to detail. Team player, proactive, quick learner, and independent worker. Location: RomeVISA NOT SPONSOREDOur Commitment to Diversity, Equity & InclusionWe ensure our workforce represents the communities we serve and create an environment where our people feel they belong. Equal Opportunity EmployerColgate is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to any characteristic protected by law.

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