Regulatory Affairs Associate

Cali - Colombia

Monthly Salary: Not Disclosed

Posted on: Yesterday

Vacancies: 1 Vacancy

Job Summary

No Relocation Assistance Offered
Job Number#170012 - Cali Valle del Cauca Colombia

Who We Are

Colgate-Palmolive Company is a global consumer products company operating in over 200 countries specialising 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 valuesCaring Inclusive and Courageouswe foster a culture that inspires our people to achieve common goals. Together lets build a brighter healthier future for all.

Position Purpose

The Regulatory Affairs Associate is responsible to support the implementation of regulatory strategies for the commercialization and regulatory compliance of products in Colombia according to the local regional and LatAm business plans as well as the maintenance of product compliance during the whole life-cycle. The role provides support for the registration of local and imported products in the Andean Region countries and those others that import products from CP Cali manufacturing site.

Key Responsibilities

Preparation of dossiers and submission according to Colgate Palmolive standards to ensure local and imported products registration and life-cycle maintenance at INVIMA.
Working cross-functionally with internal stakeholders at regional and local level to ensure business objectives are met through strong regulatory strategy and partnership.
Proactively identifying regulatory requirements and risks for product categories (medical devices cosmetics and household products) and developing plans for regulatory submissions and products compliance.
Review of artworks and other delivered documents to ensure regulatory product compliance through the different systems of the company.
Preparation of the core dossier and support to the registration of the local and imported products in Andean Region -Bolivia Ecuador and Peru - and also for those countries that import products from CP Cali manufacturing site.
Work closely with the LatAm Regulatory Team to receive the appropriate dossier requirements support and provide the projects status update and needed registration data for labeling and LatAm strategies.
Supporting the responses to regulatory assessments and elaborate regulatory alerts concerning Colombia. Support and backup in trade association activities.
Update and maintain registration and other databases so tracking tools.

Experience and qualifications

BS degree in Pharmaceutical Chemistry
Minimum of 2 years of regulatory affairs experience in the cosmetic or pharmaceutical industry with a track record of successful submissions. Experience with medical devices is desirable.
Minimal supervision to execute tasks in a timely manner
Attention to detail and sense of urgency able to prioritize tasks
Excellent communication and organizational skills
Solid interpersonal and relationship-building skills
Ability to collaborate with multiple stakeholders both internally and externally.
Effective regulatory writing skills
Fluent in English
Excellent digital literacy which includes working with databases software MS Office applications and Google applications/tools.

Our Commitment to Inclusion
Our journey begins with our peopledeveloping strong talent with diverse backgrounds and perspectives 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 colour 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.

#LI-On-site

Required Experience:

No Relocation Assistance OfferedJob Number#170012 - Cali Valle del Cauca ColombiaWho We AreColgate-Palmolive Company is a global consumer products company operating in over 200 countries specialising in Oral Care Personal Care Home Care Skin Care and Pet Nutrition. Our products are trusted in more h...

Position Purpose

Key Responsibilities

Preparation of dossiers and submission according to Colgate Palmolive standards to ensure local and imported products registration and life-cycle maintenance at INVIMA.
Working cross-functionally with internal stakeholders at regional and local level to ensure business objectives are met through strong regulatory strategy and partnership.
Proactively identifying regulatory requirements and risks for product categories (medical devices cosmetics and household products) and developing plans for regulatory submissions and products compliance.
Review of artworks and other delivered documents to ensure regulatory product compliance through the different systems of the company.
Preparation of the core dossier and support to the registration of the local and imported products in Andean Region -Bolivia Ecuador and Peru - and also for those countries that import products from CP Cali manufacturing site.
Work closely with the LatAm Regulatory Team to receive the appropriate dossier requirements support and provide the projects status update and needed registration data for labeling and LatAm strategies.
Supporting the responses to regulatory assessments and elaborate regulatory alerts concerning Colombia. Support and backup in trade association activities.
Update and maintain registration and other databases so tracking tools.

Experience and qualifications

BS degree in Pharmaceutical Chemistry
Minimum of 2 years of regulatory affairs experience in the cosmetic or pharmaceutical industry with a track record of successful submissions. Experience with medical devices is desirable.
Minimal supervision to execute tasks in a timely manner
Attention to detail and sense of urgency able to prioritize tasks
Excellent communication and organizational skills
Solid interpersonal and relationship-building skills
Ability to collaborate with multiple stakeholders both internally and externally.
Effective regulatory writing skills
Fluent in English
Excellent digital literacy which includes working with databases software MS Office applications and Google applications/tools.