Associate, Regulatory Affairs

Relocation Assistance Offered Within Country
Job Number #169009 - Mumbai, Maharashtra, India

**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.

**Brief introduction - Role Summary/Purpose**:
- This position will manage and maintain product compliance during the whole life-cycle, for any category of products. This position will report to the Team Lead, Regulatory Operations.Engage proactively with diverse cross-functional teams, including R&D, legal, regulatory, and marketing departments, to meticulously develop and rigorously review all ingredient lists. This collaborative effort is crucial to guarantee the utmost accuracy and comprehensiveness of each list, ensuring full compliance with all relevant regulations and internal company standards. The objective is to achieve complete alignment across all stakeholders, from initial concept to final product launch, preventing discrepancies and ensuring transparency.

**Responsibilities**:
- Responsible for developing/reviewing accurate and comprehensive ingredient lists while collaborating closely with cross-functional stakeholders to ensure alignment and timely updates. Manage and maintain a detailed tracking system to monitor ingredient list status, changes and requirements, facilitating smooth communication and efficient project progress.-
- Support the regulatory strategy defined at Regional and/or Global level, and report regularly the progress to the Regional Regulatory Affairs Department with relevant KPIs, particularly in terms of timelines, status of supportive data required from other functions and dossier preparation.- Compile documents and information required for high quality and successful submissions, license renewals and annual registrations, and maintenance of product registration dossiers for Authorities and Notified Bodies.- Keep track of outstanding documentation and open queries from Authorities, and notify the relevant Regional Regulatory Affairs manager in a timely manner.- Update and maintain product registration and ingredients archives, databases and tracking tools.- Upload and maintain as required by the Regional RA team any documentation supporting the placing of the market of other categories of products eg cosmetics, home care, consumer goods.- Work closely with Global and third party business partners to obtain the relevant documents and information for product dossiers.- Assist in the preparation of Regulatory Standard Operation Procedures, and in keeping track of revision dates.- Manage the distribution lists of SOP and the archiving in the documentation system.

Artwork Approval:
- Assist the Regional Regulatory Affairs managers in the review of list of ingredients for labeling purposes (e.g. INCI and INDI).- Assist the Regional Regulatory Affairs managers with artwork review and approval

Regulatory intelligence and product advocacy activities:
- Understand current regulations, guidelines and standards relevant to ensure compliance to the applicable regulatory and corporate standards/requirements (medicinal products, medical devices, cosmetic products, biocides, detergents, consumer goods).- Ensure that the content, organization and overall quality of all regulatory documents are adequate and compliant with local/regional regulatory requirements, commitments and agreements.- Track Competent Authority websites and databases for news related to new product registrations.- Assist Regional Regulatory team to deliver and manage Regulatory Assessment

**Required Qualifications**:
- BS degree in Pharmacy or Life Sciences or relevant education. Advanced degree preferred.- Minimum 1 year of relevant experience in regulatory affairs, quality or product development in the pharmaceutical, medical devices or similar FMCG industries.- Understanding of registration and regulatory requirements in Africa Eurasian and Asia Pacific countries.- Knowledge of industry practices, techniques and standards.**Preferred Qualifications**:
- Good written and verbal communicator with excellent interpersonal skills.- Good planning and organizing skills.- Ability to work under stress and meet deadlines.- Fluency in spoken and written English is mandatory.- Fluency in languages is advantageous.

CPIL #LI-AP1

**Our Commitment to Inclusion**
Our journey begins with our people—developing strong talent with diverse backgrounds and perspectives to best serve our consumers around the world and fosterin