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Regulatory Affairs Analyst (Temporary)

Colgate-Palmolive Ā· Caracas, A, VE
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Caracas, A, VE
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No Relocation Assistance Offered
Job NumberĀ #175868 - Caracas, Distrito Federal, Venezuela

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.

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About the Role

Are you a detail-oriented regulatory professional eager to ensure seamless market entry for innovative consumer products? As our Regulatory Affairs Analyst, you will support end-to-end regulatory operations by compiling comprehensive product dossiers, maintaining accurate regulatory archives, and tracking project milestones. Acting as a vital connection between Regulatory Affairs, R&D, and International Marketing, you will streamline technical communication, document Standard Operating Procedures (SOPs), and ensure full alignment with local and international regulatory landscapes. If you bring strong organizational skills, cross-functional agility, and a passion for regulatory compliance in CPG, this role is a fantastic opportunity to advance your career!

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Core Responsibilities:

  • Dossier Management: Assemble, review, and compile comprehensive regulatory submission dossiers required for new product launches, line extensions, and market expansions.

  • Cross-Functional Collaboration: Partner closely with internal Regulatory, International Marketing, and R&D teams to streamline information flow and ensure technical alignment across project timelines.

  • Process & SOP Documentation: Assist in drafting, updating, and maintaining Standard Operating Procedures (SOPs) and Work Instructions for evolving regulatory processes to guarantee compliance and operational consistency.

  • Tracking & Archive Management: Maintain up-to-date product information archives, tracking tools, and regulatory databases to ensure full traceability and data integrity.

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Required Qualifications:

  • Bachelor’s degree in Pharmacy, Pharmaceutical Biological Chemistry (QFB), Chemical Engineering, or a closely related field.

  • Minimum 1 year of experience in Regulatory Affairs or similar regulatory roles (including internships).

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Preferred Qualifications:

  • Intermediate English proficiency.

  • Proficiency in Google Workspace tools and Microsoft Office Suite.

  • Experience within the Consumer Packaged Goods (CPG), cosmetics, personal care, or food manufacturing industries.

  • Strong background in regulatory data management, product archive tracking, and knowledge of the global/regional regulatory landscape.

  • Strong planning, prioritization, organization, and cross-functional communication skills.

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Note: This is a temporary position for a period of 6 months.


Our Commitment to Inclusion
Our journey begins with our people—developing strong talent with diverse backgrounds and perspectives Ā to best serve our consumers around the world and fostering an inclusive environment where everyone feels a true sense of belonging. We are dedicated to ensuring that each individual can be their authentic self, is treated with respect, and is empowered by leadership to contribute meaningfully to our business.



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 complete this request form should you require accommodation.

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