Regulatory Affairs Manager, Se

4 settimane fa


Roma, Italia Colgate-Palmolive A tempo pieno

No Relocation Assistance Offered
Job Number #164255 - Roma, Lazio, Italy

**Who We Are**

Colgate-Palmolive Company is a global consumer products company operating in over 200 countries specializing in Oral Care, Personal Care, Home Care, Skin Care, and Pet Nutrition. Our products are trusted in more households than any other brand in the world, making us a household name

Join Colgate-Palmolive, a caring, innovative growth company reimagining a healthier future for people, their pets, and our planet. Guided by our core values—Caring, Inclusive, and Courageous—we foster a culture that inspires our people to achieve common goals. Together, let's build a brighter, healthier future for all.

**The Regulatory Affairs function plays a crucial role in ensuring that Company's products comply with all the relevant regulations in the selling markets; preparing, reviewing, and submitting regulatory documentation to the local competent authorities/agencies; acting as the primary point of contact between the Company and regulatory authorities; keeping abreast of changes in regulatory legislation and guidelines that may affect the Company’s products and advising other departments on the implications of these changes.**

**The Regulatory Affairs Manager SE**reports direct to the Senior Regulatory Affairs Manager, here below**

**the main r**esponsibilities**:

- ** Stay abreast of the current and the incoming European / National (i.e. Italy, Spain, Portugal, Greece and Cyprus) regulatory framework relevant to Colgate’s portfolio (detergents, biocides, cosmetics, medicinal products and medical devices) with a primary focus on personal care cosmetic products.**:

- ** Represent Colgate’s interests in the local / EU Trade Associations and Consortia in alignment with the defined strategies.**
- ** Maintain key business partners constantly informed on the current and the evolving regulatory requirements relevant to Colgate’s portfolio in a well-structured, straightforward and comprehensive manner.**
- ** Support in the provision of expert regulatory assessments and inputs to strategic decision making and ensure that regulatory strategies and activities are effectively executed to meet the business objectives and legal requirements, in close collaboration with internal stakeholders.**
- ** Provide regulatory support on day-to-day issues, new initiatives and developments (eg. revision of the EU Cosmetic Products Regulation), including training to internal stakeholders in topics related to the products and projects under his/her responsibility**
- ** Write comprehensible, clear Regulatory Assessments and documents for internal and external stakeholders (eg. Authorities and Trade Associations).**
- ** Ensure regulatory compliance and maintenance of all product registrations and licenses throughout the whole life-cycle of the products under his/her responsibility.**
- ** Establish strong relationships within the European Division, Regulatory Operations and Global Partners on a cross-functional basis including Marketing, Legal, Technical, Supply Chain, R&D, Regulatory and Product Safety, to ensure alignment and synchronization between Regulatory strategies and Business goals.**
- ** Provide assistance to authority inspections in the matters under Regulatory responsibility.**
- ** Ensure the review and approval of artworks for products and territories under his/her responsibility.**
- ** Provide input for budget preparation and reviews.**
- ** Collaborate in regional and global regulatory projects and act as a project manager in the projects assigned to him/her.**
- ** Contribute to an effective use of the network of regulatory consultants, including coordination with procurement and legal for contract negotiations and FCPA and Due Diligence processes.**

**Requirements**:

- ** Bachelor or Masters in science, pharmacy, medicine, or law.**
- ** Preferred: Advanced degree (PhD, PharmD) in science, pharmacy, medicine, or law.**
- ** A minimum of 4-5 years in regulatory affairs and/or regulatory intelligence and experience in managing regulatory policy activities is ideal (i.e. within industry, professional organization or trade associations). Specific experience on personal care products portfolio will be considered a plus**
- ** Languages: Fluent in Italian language and fluent in English language. Will be considered a plus the**knowledge of Spanish, Portuguese or Greek.**

**Competencies Required**:

- ** Excellent working knowledge of the European markets and of the European regulators and other key associations and organizations (in the FMCG arena).**
- ** Successful track record demonstrating an ability to analyze new regulations or policies and assess the impact on the FMCG business or New Product Development programs.**
- ** Ability to work in collaborative, matrixed environments, across different businesses and cultures on a worldwide basis.**
- ** Strategic thinking, data and impact analysis, and excellent oral and written co



  • Roma, Italia Mantell Associates A tempo pieno

    Managing Associate - Clinical Research & Development | Biotech & Pharma at Mantell Associates Mantell Associates is partnered with a Cell & Gene Therapy organisation, who is seeking a CMC Regulatory Affairs Manager to join their growing team. CMC Regulatory Affairs Manager - Responsibilities: Help the team implement and manage CMC regulatory strategies...


  • Roma, Lazio, Italia Meditrial A tempo pieno

    Industry: Lifescience Industry: Medtech, Digital HealthEmployment Type: Full-timeJob Functions: Regulatory AffairsLocation: Meditrial, Via Po 9 Rome, ItalyWorkplace: Office-based / availability to travelThe Regulatory Affairs Manager oversees the regulation process for products (Medical Device and Marketing Authorization) requiring governmental...


  • Roma, Lazio, Italia TN Italy A tempo pieno

    Company OverviewTN Italy is a leading pharmaceutical company with a strong presence in the European market.Our mission is to provide innovative solutions for patients and healthcare professionals.Job DescriptionAs a Regulatory Affairs Project Manager, you will be responsible for managing regulatory projects from start to finish.Responsibilities...


  • Roma, Lazio, Italia Meditrial A tempo pieno

    Job DescriptionAs a key member of the Meditrial team, the Regulatory Affairs Manager will oversee the regulation process for products requiring governmental approval. This includes filing necessary applications and handling government interactions to ensure compliance with regulatory requirements.Key Responsibilities:Collaborate on implementations of...


  • Roma, Italia PQE Group A tempo pieno

    Sei pronto per entrare a far parte di una società di consulenza leader mondiale nell'industria farmaceutica e dei Medical Device ? PQE Group è affermata in questo settore dal 1998 , garantendo una presenza internazionale grazie alle 45 filiali e i 2000 dipendenti in Europa, Asia e nelle Americhe. Lavorare in una realtà di consulenza come PQE Group...


  • Roma, Italia PQE Group A tempo pieno

    Sei pronto per entrare a far parte di una società di consulenza leader mondiale nell'industria farmaceutica e dei Medical Device ? PQE Group è affermata in questo settore dal 1998 , garantendo una presenza internazionale grazie alle 45 filiali e i 2000 dipendenti in Europa, Asia e nelle Americhe. Lavorare in una realtà di consulenza come PQE Group...


  • Roma, Italia PQE Group A tempo pieno

    Sei pronto per entrare a far parte di una società di consulenza leader mondiale nell'industria farmaceutica e dei Medical Device ? PQE Group è affermata in questo settore dal 1998 , garantendo una presenza internazionale grazie alle 45 filiali e i 2000 dipendenti in Europa, Asia e nelle Americhe. Lavorare in una realtà di consulenza come PQE Group...


  • Roma, Italia PQE Group A tempo pieno

    Sei pronto per entrare a far parte di una società di consulenza leader mondiale nell'industria farmaceutica e dei Medical Device ? PQE Group è affermata in questo settore dal 1998 , garantendo una presenza internazionale grazie alle 45 filiali e i 2000 dipendenti in Europa, Asia e nelle Americhe. Lavorare in una realtà di consulenza come PQE...


  • Roma, Lazio, Italia The Kraft Heinz Company A tempo pieno

    Job DescriptionWe have an exciting opportunity available for a Regulatory Affairs Manager in Italy.The position is based in Milan, where you will be working in an impactful team, alongside stakeholders that are always trying to reach the next level. You will be part of the Legal, Government and Regulatory Affairs department, reporting to the European...


  • Roma, Italia Meditrial Europe Ltd. A tempo pieno

    Meditrial is a full-service clinical research organization (CRO) dedicated to clinical trial conduct, medical education, regulatory affairs, and market access. Our offices are located in Germany, Italy, Switzerland, the UK, and the United States, and our teams rely on digital tools to work collaboratively to achieve shared goals. Since 2008, Meditrial...


  • Roma, Italia ProductLife Group A tempo pieno

    Intexo, parte del Gruppo PLG, è alla ricerca di un/una Regulatory Affairs Officer con almeno due anni di esperienza nel ruolo, da inserire nella propria sede di Roma. Chi siamo Intexo Società Benefit, una realtà di consulenza del gruppo Product Life, opera nel settore healthcare con l’obiettivo di garantire un accesso rapido, trasparente e...


  • Roma, Italia ProductLife Group A tempo pieno

    Intexo, parte del Gruppo PLG, è alla ricerca di un/una Regulatory Affairs Officer con almeno due anni di esperienza nel ruolo, da inserire nella propria sede di Roma. Chi siamo Intexo Società Benefit, una realtà di consulenza del gruppo Product Life, opera nel settore healthcare con l’obiettivo di garantire un accesso rapido, trasparente e...


  • Roma, Italia ProductLife Group A tempo pieno

    Intexo, parte del Gruppo PLG, è alla ricerca di un/una Regulatory Affairs Officer con almeno due anni di esperienza nel ruolo, da inserire nella propria sede di Roma. Chi siamo Intexo Società Benefit, una realtà di consulenza del gruppo Product Life, opera nel settore healthcare con l’obiettivo di garantire un accesso rapido, trasparente e...


  • Roma, Italia ProductLife Group A tempo pieno

    Intexo, parte del Gruppo PLG, è alla ricerca di un/una Regulatory Affairs Officer con almeno due anni di esperienza nel ruolo, da inserire nella propria sede di Roma. Chi siamo Intexo Società Benefit, una realtà di consulenza del gruppo Product Life, opera nel settore healthcare con l’obiettivo di garantire un accesso rapido, trasparente e sostenibile...


  • Roma, Lazio, Italia JR Italy A tempo pieno

    As a regulatory affairs specialist with JR Italy, you will play a vital role in supporting the company's growth and success in the Italian market. We are looking for a highly motivated and organized individual to manage regulatory activities for our portfolio of products.Key Responsibilities:Contribute to local regulatory affairs activities for ItalyManage...


  • Roma, Italia Pharma D&S A tempo pieno

    Regulatory Affairs Consultant Pharma D&S ricerca, per la sede di Roma, un/una Regulatory Affairs Consultant con almeno 2/3 anni di esperienza nel ruolo: La risorsa selezionata si occuperà di: - Collaborare alla definizione della strategia regolatoria - Preparare la documentazione di Qualità (Modulo 3 e 2.3) - Preparare la domanda di deposito di un Master...


  • Roma, Italia Pharma D&S A tempo pieno

    Regulatory Affairs Consultant Pharma D&S ricerca, per la sede di Roma, un/una Regulatory Affairs Consultant con almeno 2/3 anni di esperienza nel ruolo: La risorsa selezionata si occuperà di: - Collaborare alla definizione della strategia regolatoria - Preparare la documentazione di Qualità (Modulo 3 e 2.3) - Preparare la domanda di deposito di un Master...


  • Roma, Italia Meditrial Europe Ltd. A tempo pieno

    Meditrial is a full-service clinical research organization (CRO) dedicated to clinical trial conduct, medical education, regulatory affairs and market access. Our offices are located in Germany, Italy, Switzerland, UK, United States and our teams rely on digital tools to work collaboratively to achieve shared goals. Since 2008, Meditrial delivers...


  • Roma, Italia Colgate A tempo pieno

    Job Title: Regulatory Affairs Manager, SETravel Required?: Travel - 25% of timeDate: Feb 20, 2025HybridNo Relocation Assistance OfferedJob Number#164255 - Roma, Lazio, ItalyWho We AreColgate-Palmolive Company is a global consumer products company operating in over 200 countries specializing in Oral Care, Personal Care, Home Care, Skin Care, and Pet...


  • Roma, Italia ProductLife Group A tempo pieno

    Intexo, parte del Gruppo PLG, è alla ricerca di un/una Regulatory Affairs Officer con almeno due anni di esperienza nel ruolo, da inserire nella propria sede di Roma. Chi siamo Intexo Società Benefit, una realtà di consulenza del gruppo ProductLife, opera nel settore healthcare con l’obiettivo di garantire un accesso rapido, trasparente e...