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1–2 jobs· newest first

Regulatory Affairs Manager – CMCNew
Procter & Gamble · Mexico City, Mexico
On-site · Full-time · Manager
Regulatory Affairs Manager – CMCNew
Procter & Gamble · Huixquilucan, Mexico+1 more
Full-time

+10K new in the last hour

Regulatory Affairs Manager – CMC

Procter & Gamble · Posted Nov 11, 2026

Mexico City, Mexico City, Mexico
On-site
Full-time · Manager

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AI

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Lead the preparation, review, and approval of technical regulatory documentation supporting product renewals, variations, new registrations, and rollouts across Latin America.

Responsibilities

Plan, author, coordinate, and review submission-ready CMC technical documentation for medicinal products and food supplements, including CTD Modules 2.3 and 3 and Food Supplement Master Dossiers.
Ensure technical documents are accurate, complete, consistent, scientifically sound, and compliant with applicable CTD standards and regulatory requirements.
Maintain alignment between submission documentation, manufacturers' information, and supporting technical/raw data.
Upload and maintain regulatory documentation in Veeva RIM or applicable document management systems and coordinate stakeholder review and approval.
Serve as the primary point of contact for questions and feedback related to assigned technical documents, including content and formatting.

Requirements

University degree in Pharmacy, Pharmaceutical Sciences, Chemistry, Life Sciences, or another relevant scientific field
Nice to have: Latin American regulatory requirements knowledge
Nice to have: Marketing authorizations experience
Nice to have: Veeva RIM experience
Nice to have: Spanish language proficiency

Skills

Regulatory Affairs CMC CTD guidelines Project management Communication Veeva RIM

Benefits

Continuous mentorship
Formal training
Agility and work/life balance
Competitive salary and benefits' package

See full job description

Regulatory Affairs Manager – CMC

Procter & Gamble · Posted Nov 11, 2026

Huixquilucan, México, Mexico +1 more
Full-time

Apply with RefersoAI Apply on careers page

Lead the preparation, review, and approval of technical regulatory documentation supporting product renewals, variations, new registrations, and rollouts across Latin America.

Locations (2)

Huixquilucan, México, Mexico
Mexico City, Mexico City, Mexico

Compensation

We will give you a competitive salary and benefits' package.

Responsibilities

Plan, author, coordinate, and review submission-ready CMC technical documentation for medicinal products and food supplements
Ensure technical documents are accurate, complete, consistent, scientifically sound, and compliant with applicable CTD standards and regulatory requirements
Maintain alignment between submission documentation, manufacturers' information, and supporting technical/raw data
Upload and maintain regulatory documentation in Veeva RIM or applicable document management systems and coordinate stakeholder review and approval
Serve as the primary point of contact for questions and feedback related to assigned technical documents

Requirements

University degree in Pharmacy, Pharmaceutical Sciences, Chemistry, Life Sciences, or another relevant scientific field
Nice to have: Knowledge of Latin American regulatory requirements
Nice to have: Experience with marketing authorizations
Nice to have: Experience supporting innovation projects
Nice to have: Spanish language proficiency

Skills

Regulatory Affairs Quality Assurance CMC Product Development CTD guidelines Project management Stakeholder management Technical documentation Veeva RIM document management systems

Benefits

Mentorship
Flexible work schedule
Work/life balance
Competitive salary and benefits package

See full job description