Product Safety & Regulatory Affairs LATAM Analyst

Henkel; Región Centro; On-site; MXN 320,000 - 520,000; Full time

Benefits offered by this job

Global wellbeing standards

Parental leave

Employee Share Plan

Flexible Benefits

Canteen

Savings Fund

Job summary

Henkel is seeking a PSRA Specialist to ensure regulatory compliance and support the registration, maintenance, and commercialization of cosmetics across LATAM. You will partner with Marketing, R&D, Quality, Supply Chain, Manufacturing, and external authorities to manage registrations and submissions.

You will review formulas, labeling, and artwork for LATAM compliance, maintain dossiers and certificates, and guide internal teams through the product lifecycle.

Qualifications

• Bachelor's degree or higher in a scientific field with emphasis on regulatory affairs.

Responsibilities

• Manage the preparation, submission, and maintenance of cosmetic product registrations and notifications across LATAM markets.
• Coordinate regulatory activities to support product launches, reformulations, line extensions, renewals, and discontinuations.
• Review product formulas, claims, artwork, and labeling for LATAM regulatory compliance.
• Maintain regulatory documentation, technical dossiers, certificates, and data for health authorities and databases.
• Provide regulatory guidance to internal stakeholders throughout the product lifecycle.
• Support regulatory projects related to compliance improvements and process optimization.
• Communicate regulatory risks, opportunities, and project status to stakeholders.

Skills

Fluent English

Spanish

Project management

Stakeholder management

Education

Bachelor's degree in Pharmaceutical Biochemistry Sciences or a related scientific field

Tools

Regulatory databases

Microsoft Office

Job description

About this Position

The PSRA Specialist is responsible for ensuring regulatory compliance and supporting the successful registration, maintenance, and commercialization of cosmetic products across Latin America.

This role partners closely with cross-functional teams including Marketing, R&D, Quality, Supply Chain, Manufacturing, and external authorities to manage product registrations, regulatory submissions, label compliance, and post-approval changes.

The position plays a key role in enabling business growth by ensuring products meet applicable regulatory requirements while supporting innovation, portfolio expansion, and operational excellence.

What you´ll do

• Manage the preparation, submission, and maintenance of cosmetic product registrations and notifications across LATAM markets.


• Coordinate regulatory activities to support new product launches, reformulations, line extensions, renewals, and product discontinuations.


• Review and assess product formulas, claims, artwork, labels, to ensure compliance with LATAM region regulatory requirements.


• Maintain regulatory documentation, technical dossiers, certificates, and supporting data required by health authorities, and databases


• Provide regulatory guidance to internal stakeholders, ensuring compliance throughout the product lifecycle.


• Support implementation of regulatory projects related to compliance improvements, digitalization initiatives, and process optimization.


• Ensure timely communication of regulatory risks, opportunities, and project status to stakeholders.

What makes you a good fit

• Education:Bachelor's degree in Pharmaceutical Biochemistry Sciences or a related scientific field.


• Professional Experience:6 - 12 months of experience in Regulatory Affairs, Product Safety, or Compliance within the cosmetics, personal care, pharmaceutical, consumer health, or related industries.


• Experience managing product registrations and regulatory submissions across multiple Latin American countries.


• Knowledge of cosmetic regulations, labeling requirements, and product compliance processes.


• Experience working with cross-functional and regional teams.


• Technical Skills:Strong understanding of cosmetic regulatory frameworks and product lifecycle management.


• Experience reviewing product formulas, claims substantiation, artwork, and labeling.


• Proficiency in Microsoft Office applications, particularly Excel, PowerPoint, and Teams.


• Experience with regulatory databases and document management systems is preferred.


• Ability to analyze regulatory requirements and translate them into practical business actions.


• Soft Skills:Strong project management and organizational skills.


• Excellent attention to detail and accuracy.


• Ability to manage multiple priorities in a fast-paced environment.


• Effective communication and stakeholder management skills.


• Strong problem-solving and critical-thinking capabilities.


• Ability to work independently while maintaining strong collaboration across teams.


• Results-oriented mindset with a continuous improvement approach.


• Language Requirements:Fluent English (written and spoken).Spanish required.

Some perks of joining Henkel

• Global wellbeing standards with health and preventive care programs


• Gender-neutral parental leave for a minimum of 8 weeks


• Employee Share Plan with voluntary investment and Henkel matching shares


• Flexible Benefits


• Canteen


• Savings Fund

At Henkel, we come from a broad range of backgrounds, perspectives, and life experiences. We believe the uniqueness of all our employees is the power in us. Become part of the team and bring your uniqueness to us! We welcome all applications across different genders, origins, cultures, religions, sexual orientations, disabilities, and generations.