Abbott Posted October 15, 2026

Director Regulatory Affairs LATAM, EPD (m/f/d)

Sao Paulo, São Paulo, Brazil FULL_TIME
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Abbott is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

At Abbott, we're committed to helping people live their best possible life through the power of health. For more than 125 years, we've brought new products and technologies to the world in nutrition, diagnostics, medical devices and branded generic pharmaceuticals that create more possibilities for more people at all stages of life. Today, 114,000 of us are working to help people live not just longer, but better, in the more than 160 countries we serve.

Abbott’s Established Pharmaceuticals Division (EPD) is looking to recruit a:

Director Regulatory Affairs LATAM (m/f/d)

Based in Sao Paulo or Rio de Janeiro, Brazil

Primary Job Function:

Provide strategic leadership for Regulatory Affairs across LATAM, driving regulatory excellence and business growth through effective regulatory strategies, external influence, and strong organizational leadership.

Build and develop a high-performing matrix organization across affiliates and regional teams, fostering a culture of accountability, ownership, collaboration, and continuous improvement.

Act as a senior representative of Abbott with health authorities, industry associations, and key stakeholders, shaping the external regulatory environment while ensuring alignment between regulatory priorities and commercial objectives.

Core Job Responsibilities

Combined knowledge of scientific, regulatory and business issues to develop products to meet required regional and local regulatory requirements.

Develop a comprehensive regulatory external engagements stakeholder management strategy with leadership of regional heads and other key stakeholders of each of the business units of EPD in LATAM.

Coordinate and execute strategies related to regulatory intelligence and policy, advocating Abbot’s position with Regulatory Agencies and related policy influencer groups.

In collaboration with Development build advocacy positions with scientific / academic institutions and / or Regulatory Agencies to promote Abbott science.

Supervisory/Management Responsibilities:

Direct Reports: Up to 7 direct reports

Indirect Reports: Up to 20 indirect reports

Dotted line: Up to 11 dotted Line reports

Position Accountability/Scope:

Strategic leadership of regulatory activities across LATAM, including development, registration, and LCM for EPD products.

Sales Impact: Supports a commercial portfolio, ensuring regulatory continuity and enabling new launches.

Budget Responsibility: Oversees a regulatory budget, covering agency interactions, and compliance activities.

Representing the company in interactions with health authorities and industry associations to influence regulatory policy and harmonization efforts.

Minimum Education

Bachelor’s degree in related scientific discipline or Advanced degree (MS including MS RA, MEng, Ph.D.) in scientific discipline preferred.

Minimum Experience/Training Required:

Demonstrated strategic leadership capability in shaping and executing complex regulatory strategies across multiple markets, ensuring alignment with business priorities, growth objectives, and portfolio ambitions across LATAM.

Proven track record of influencing and engaging senior regulatory authorities, industry associations, and policy-shaping stakeholders, successfully advancing regulatory frameworks, policy positions, and business-critical initiatives.

Recognized leader with the ability to build organizational capability through a strong culture of accountability, ownership, performance excellence, and transparent decision-making, driving sustained results across geographically dispersed teams.

Demonstrated success in leading large, complex matrix organizations, aligning regional, affiliate, global, and cross-functional stakeholders behind common objectives while effectively managing competing priorities.

Strong ability to develop, coach, and empower affiliate regulatory leaders, creating high-performing teams and strengthening organizational capability across the region.

Proven experience establishing and maintaining influential partnerships with affiliate leadership, commercial organizations, medical affairs, quality, supply chain, and global regulatory functions to accelerate business outcomes.

Track record of successfully driving organizational transformation, fostering collaboration across countries and functions, and creating an environment where teams take ownership, proactively solve problems, and deliver with urgency.

Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity.

Connect with us at www.abbott.com , on Facebook at www.facebook.com/Abbott and on X @AbbottNews and @AbbottGlobal.

Job details

Seniority
Director
Function
Regulatory Affairs
Therapeutic area
Not listed
Location
Sao Paulo, São Paulo, Brazil
Employment type
FULL_TIME

How this role compares

Computed from every other active Regulatory Affairs role in our database, not just this employer's listings.

We currently track 98 comparable Director Regulatory Affairs roles across 40 biopharma companies.

98Comparable roles tracked
89Currently active
40Companies hiring similar roles
16Countries represented

Salary context

45 of 98 peers report a salary range (USD, annualized)

Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.

This roleSubject Not listed on this posting
Peer group range $119,000 – $322,900 (median $264,000)

Where these roles are based

Top locations among the 98 comparable roles

United States70
United Kingdom6
Ireland5
China2
Japan2
Spain2

+ 10 more countries

Seniority mix

98 of 98 peers have a known seniority level

Director67
Senior Director18
Principal13

Therapeutic area mix

16 of 98 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Oncology5
Rare Disease5
Vaccines & Infectious Disease2
Cardiovascular / CVRM2
Neuroscience1
Immunology1

Similar opportunities

The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

45%similar
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Notify me about similar jobs

Get an email when we spot other openings like this one – same job function, comparable seniority, roles you'd actually want to see.

How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

45%
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Function Therapeutic area Seniority Country
45%
Director, RA Global Regulatory Strategy
AbbVie · Florham Park, NJ · Director
Function Therapeutic area Seniority Country
45%
Director, Regulatory Strategist
Mylan Inc. · Washington, United States · Director
Function Therapeutic area Seniority Country
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Function Therapeutic area Seniority Country
Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.