REGULATORY AFFAIRS ASSOCIATE MANAGER JOB DETAILS

No Relocation Assistance Offered #  - Warsaw, Mazovia, Poland Who We Are Colgate-Palmolive Company is a caring, innovative growth company that is reimagining a healthier future for all people, their pets and our planet.
Focused on Oral Care, Personal Care, Home Care and Pet Nutrition, we sell our products in more than 200 countries and territories under brands such as Colgate, Palmolive, elmex, hello, meridol, Sorriso, Tom’s of Maine, EltaMD, Filorga, Irish Spring, PCA SKIN, Protex, Sanex, Softsoap, Speed Stick, Ajax, Axion, Fabuloso, Soupline and Suavitel, as well as Hill’s Pet Nutrition.
We are recognised for our leadership and innovation in promoting sustainability and community wellbeing, including our achievements in decreasing plastic waste and promoting recyclability, saving water, conserving natural resources and improving children’s oral health.
If you want to work for a company that lives by their values, then give your career a reason to smile and join our global team!   Job Title.
Regulatory Affairs Specialist / Manager  - Medicinal Products Scope.
This regulatory position has European responsibilities on medicinal products for Europe.
Location.
Poland (Warsaw) Reporting.
This position reports to the Senior Regulatory Affairs Manager responsible for Oral Care Direct Reports.
None Travel.
<10%     Responsibilities.
Establish and maintain overview and exchange on current and evolving regulatory requirements in Europe, with primary focus on medicinal products.
Provide expert regulatory input to strategic decision making, and ensure that regulatory strategies and regulatory activities are effectively executed to meet the business objectives and legal requirements, in close collaboration with Regulatory Operations and other internal stakeholders.
Manage the maintenance activities potentially including Life Cycle Management strategy for  medicinal products in Europe, and in collaboration with the Regulatory Operations.
Ensure regulatory compliance and maintenance of all product registrations and licenses throughout the whole life-cycle of the products under his/her responsibility.
Ensure timely submission of high quality responses to queries raised by regulatory agencies and follow up on these requests.
Provide support to the Regulatory Affairs Managers in the hubs in topics related to medicinal products.
Write comprehensible, clear Regulatory Assessments and documents for internal and external stakeholders (eg.
Authorities and trade Associations).
Competencies Required.
Relevant Master degree in Pharmacy, Biology, Chemistry or equivalent Minimum 3-5 years of Regulatory Affairs experience in an international environment, FMCG preferred, in the field of Medicinal Products.
Fluency in English.
Additional European language is a plus.
Good analytical skills and technical/ scientific competence Strong organizational skills Attention to details and ability to appropriately assess the regulatory impact and formulate actionable strategy, including taking “the big picture” view on various options Effective communication, keeping people well informed of plans, goals and objectives, and sharing information openly Responds to day-to-day issues and problems with simple, timely and practical solutions.
Our Commitment to Sustainability With the Colgate brand in more homes than any other, we are presented with great opportunities and new challenges as we work to integrate sustainability into all aspects of our business and create positive social impact.
We are determined to position ourselves for further growth as we act on our Sustainability & Social Impact Strategy.
Our Commitment to Diversity, Equity & Inclusion Achieving our purpose starts with our people — ensuring our workforce represents the people and communities we serve —and creating an environment where our people feel they belong; where we can be our authentic selves, feel treated with respect and have the support of leadership to impact the business in a meaningful way.
Equal Opportunity Employer Colgate is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity, sexual orientation, national origin, ethnicity, age, disability, marital status, veteran status (United States positions), or any other characteristic protected by law.
Reasonable accommodation during the application process is available for persons with disabilities.
Please contact with the subject "Accommodation Request" should you require accommodation.
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