BSc Life Sciences Jobs in Regulatory Affairs at Colgate-Palmolive
Are you passionate about regulatory affairs and eager to build a rewarding career with a global leader? Colgate-Palmolive is hiring an Associate, Regulatory Affairs in Mumbai, India. This hybrid role offers you the opportunity to contribute to product compliance, collaborate with cross-functional teams, and ensure regulatory excellence across multiple categories. Join us in shaping a healthier, sustainable future while advancing your career in a world-renowned consumer products company.
- Job Title: Associate, Regulatory Affairs
- Location: Mumbai, Maharashtra, India
- Mode: Hybrid Mode
- Travel Required: Up to 10%
- Job Number: #169009
About Colgate-Palmolive
Colgate-Palmolive is a trusted global company operating in over 200 countries, specializing in Oral Care, Personal Care, Home Care, Skin Care, and Pet Nutrition. Our products are household favorites worldwide, and we are committed to reimagining a healthier future for people, pets, and the planet. Guided by our values—Caring, Inclusive, and Courageous—we empower our teams to drive innovation and growth.
Role Summary
As an Associate in Regulatory Affairs, you will manage product compliance throughout the entire lifecycle across multiple categories. Reporting to the Team Lead, Regulatory Operations, you will collaborate with R&D, legal, regulatory, and marketing teams to develop and review ingredient lists, ensuring accuracy, transparency, and compliance with global standards.
Key Responsibilities
- Develop and review ingredient lists while working with cross-functional teams.
- Track ingredient list status, changes, and requirements to ensure timely updates.
- Support the Regional Regulatory Affairs Department with new product registrations, renewals, notifications, and license applications.
- Compile documents for high-quality regulatory submissions and renewals.
- Maintain product registration dossiers, archives, and databases.
- Assist in artwork reviews, labeling compliance, and ingredient approvals.
- Conduct regulatory intelligence and advocacy by monitoring regulations and authority databases.
- Prepare and maintain SOPs and ensure timely revisions.
- Collaborate with global and third-party partners for dossier documentation.
Required Qualifications
- BS degree in Pharmacy or Life Sciences (advanced degree preferred).
- Minimum 1 year of experience in regulatory affairs, quality, or product development.
- Knowledge of Africa, Eurasian, and Asia Pacific regulatory requirements.
- Proficiency in Google Suite, MS Office, eCTD software, SAP, DMS, and regulatory databases.
- Strong organizational, planning, and communication skills.
- Fluency in English; additional languages are an advantage.
Preferred Skills
- Excellent interpersonal and teamwork abilities.
- Ability to work under pressure and meet deadlines.
- Strong documentation and compliance knowledge.
Why Join Us
At Colgate-Palmolive, inclusion and diversity are at the core of our culture. We value authenticity, respect, and collaboration, ensuring every team member feels empowered to contribute. As an equal opportunity employer, we provide reasonable accommodations during the application process for individuals with disabilities.
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