Regulatory Affairs Specialist

About this Position

We are looking for a motivated and experienced Regulatory

Affairs Specialist to join our team. This role will support regulatory

operations across key product categories throughout South America, ensuring

full compliance with local and regional regulations. The ideal candidate will

bring a strong understanding of regulatory frameworks in the region, preferably

within industries such as cosmetics, personal care, or pharmaceuticals, and

demonstrate the ability to optimize manual and operational processes using

technology and automation tools.

What you´ll do

Key

Responsibilities : Prepare,

compile, and submit regulatory dossiers in compliance with health

authorities across South America (e.g., INVIMA, ANVISA, DIGEMID, ISP).

Ensure

timely registration, renewal, and post-marketing maintenance of products

in multiple countries and categories.

Monitor

and interpret regulatory requirements in each country, keeping internal

stakeholders informed of relevant updates and changes.

Liaise

with internal departments such as R&D, marketing, and supply chain to

ensure regulatory strategies align with broader business objectives.

Support

product claims validation and labeling compliance in alignment with each

market’s regulations.

Assist

in implementing digital tools to streamline documentation, data

management, and submissions.

Contribute

to continuous improvement initiatives by identifying opportunities for

process automation and regulatory tech adoption.

What makes you a good fit

Bachelor’s

degree in Chemical Engineering, Pharmaceutical Chemistry, or a related

scientific discipline.

2+

years of experience in Regulatory Affairs, ideally within cosmetics,

personal care, pharmaceutical, or consumer goods industries.

Strong

knowledge of regulatory environments across South American countries,

including but not limited to Colombia (e.g., INVIMA), Brazil (e.g.,

ANVISA), and others.

Familiarity

with international regulations is an advantage.

Intermediate

to advanced English – must be able to hold conversations and communicate

clearly in both verbal and written form.

Proficiency

in Microsoft Office Suite (Excel, Word, PowerPoint); knowledge of digital

tools and AI technologies for process optimization is a plus.

Detail-oriented,

organized, and capable of managing multiple priorities in a dynamic,

multicultural environment.

Experience

in regulatory submissions using electronic systems or platforms.

Interest

or experience in digital transformation, AI tools, or process automation

for regulatory tasks.

Some perks of joining Henkel

• Flexible work scheme with flexible hours, hybrid work model, and work from anywhere policy for up to 30 days per year
• Diverse national and international growth opportunities
• Globally 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

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.