# Regulatory Affairs Manager – CMC at Procter & Gamble

Procter & Gamble is hiring a Regulatory Affairs Manager – CMC. Level rates it Little AI ●○○○; you can [apply on Procter & Gamble](https://jobsbylevel.com/go/a0c468eb-ef83-4dfc-86b6-063a3d404ea1?utm_medium=ai-agent).

AI Level 1, AI centrality 37 out of 100. MEXICO CITY GENERAL OFFICE.

## Details

- Company: [Procter & Gamble](https://jobsbylevel.com/companies/procter-gamble)
- AI level: AI Level 1 (score 37 out of 100)
- Location: MEXICO CITY GENERAL OFFICE
- Posted: November 11, 2026
- Apply: https://jobsbylevel.com/go/a0c468eb-ef83-4dfc-86b6-063a3d404ea1?utm_medium=ai-agent
- Free CV review for this job: https://jobsbylevel.com/cv-review?job=regulatory-affairs-manager-cmc-at-procter-gamble-caae9a

## Description

Job Location MEXICO CITY GENERAL OFFICE Job Description Important Note for Candidates: Accommodations: At P&G, we are committed to ensuring an inclusive recruitment, assessment, and selection process. If you have a disability and require any adjustments or accommodations for our assessments or any stage of the process, you will have the opportunity to briefly describe your needs when applying for the vacancy. Please note, it is important that you do not complete any assessments until we have contacted you to assist with any accommodation required. Before submitting your application, we strongly encourage you to review the following material: Hiring Process and Assessment Information . Familiarizing yourself with this content will help you be better prepared for the online assessments and enhance your chances of success. As a CMC Expert Scientist , you will lead the preparation, review, and approval of technical regulatory documentation supporting product renewals, variations, new registrations, and rollouts across Latin America . You will primarily support the Base Business portfolio, while also having the opportunity to contribute to innovation projects as needed. Working closely with Regulatory Affairs, Product Development, Analytical, Stability, Quality Assurance, and other multifunctional teams, you will help ensure high-quality dossiers, regulatory compliance, and continuity of supply across the region. Key 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. Partner with regional and global multifunctional teams to address regulatory requirements, assess risks and issues, and drive timely resolution. Manage multiple deliverables and priorities, developing clear plans and ensuring execution against agreed timelines. Support continuous improvement initiatives related to dossier quality, regulatory processes, and complex supply chains. Job Qualifications Top Qualifications University degree in Pharmacy, Pharmaceutical Sciences, Chemistry, Life Sciences , or another relevant scientific field. Experience working in a regulatory or technical environment , such as Regulatory Affairs, Quality Assurance, CMC, Product Development, or a related function. Experience preparing, reviewing, or supporting technical/regulatory documentation for medicinal products and/or food supplements. Working knowledge of CTD guidelines , particularly documentation associated with Modules 2.3 and 3 . Understanding of regulatory requirements and guidelines applicable to medicinal products and/or food supplements . Strong project management and organizational skills, with the ability to manage multiple priorities, timelines, and stakeholders . Strong collaboration and influencing skills, including the ability to work effectively across functions and regions. Ability to clearly and assertively communicate technical risks, issues, and recommended actions . Excellent written and verbal communication skills in English. Nice to Have Knowledge of Latin American regulatory requirements for medicinal products and/or food supplements. Previous experience with marketing authorizations, product registrations, renewals, or variations . Experience with Veeva RIM or similar regulatory/document management systems. Experience working with regional or global

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Source: https://jobsbylevel.com/jobs/regulatory-affairs-manager-cmc-at-procter-gamble-caae9a

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