Associate, Regulatory Affairs

Requisition ID **169532** - Posted **10/06/2025** - **Research & Development** - **India** - **Maharashtra** - **Mumbai** - **Colgate-Palmolive** - **Travel - up to 10% of time** - **On-site**

- Relocation Assistance Offered Within Country
169532 - Mumbai, Maharashtra, India

**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 recognized 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

**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.
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