Senior Specialist Regulatory Affairs (Oncology)

MSD LATAM; México; Hybride; MXN 900 000 - 1 500 000; Plein temps

Avantages offerts par ce poste

Hybrid work arrangement

Résumé du poste

MSD LATAM in Mexico City is seeking a Regulatory Affairs Manager (Senior Specialist) to lead regulatory submissions, lifecycle management, and compliance for our pharmaceutical products.

The role requires strong expertise in COFEPRIS processes, cross-functional collaboration, and a proactive regulatory strategy to support timely approvals and product launches. You will coordinate with local teams, maintain regulatory files, and drive continuous improvement across the regulatory lifecycle.

Qualifications

• Degree in Pharmacy, Life Sciences, or related field.
• Minimum of 8 years in a Registration Department or equivalent with COFEPRIS experience.
• Strong knowledge of local legislation and guidelines for pharma products.
• Excellent verbal and written communication skills.

Responsabilités

• Lead timely submission of new Marketing Authorization applications and manage regulatory queries.
• Develop and execute local action plans to support authorization, launch, and lifecycle management.
• Ensure approvals are compliant; manage variations, renewals, and post-approval changes.
• Collaborate with cross-functional teams on regulatory activities including QNs, GMP inspections, and annual product reviews.

Connaissances

Regulatory affairs management

Regulatory submissions

Project management

Pharma regulatory affairs

English proficiency

GMP inspections

Quality notifications

COFEPRIS

Regulatory strategy development

Stakeholder management

Formation

Bachelor's degree in Pharmacy / Life Sciences

Outils

Regulatory databases

Artwork Management System

Description du poste

Job Description

We are looking for a Regulatory Affairs Manager (Senior Specialist) to join our Regulatory Team in Mexico.

Position Overview

The Regulatory Affairs Manager will be responsible for ensuring the timely preparation, submission, and follow-up of new Marketing Authorization applications with the Health Authority. This role also ensures the maintenance of the regulatory status of assigned products through the timely submission of variations, renewals, and post-approval changes.

The successful candidate will stay current on pipeline submissions, applicable local regulations, and evolving guidelines, proactively developing and implementing regulatory strategies as needed. In addition, this role requires building and maintaining strong collaborative relationships with internal and external stakeholders, including regional functions and regulatory authority ( Cofepris) .

Key Responsibilities

New Marketing Authorization (MA) Applications

• Ensure the timely and high-quality submission of new MA applications.
• Lead the approval process by managing regulatory authority queries related to product registrations and major indications, and proactively negotiate to achieve optimal regulatory outcomes.
• Develop and execute local action plans to support the successful authorization, launch, and lifecycle integration of newly approved products.

Maintenance of Marketing Authorizations

• Ensure assigned marketing authorizations remain compliant with regulatory requirements by executing variations, renewals, and related activities within established timelines and standards.
• Communicate approval updates to relevant stakeholders through appropriate channels.
• For major indications, design and implement local action plans aligned with the process for new MA applications.
• CMC Post Approval Changes, variations, renewals, labelling and in general Product Life cycle management regulatory applications.

Compliance

• Provide internal stakeholders with accurate and up-to-date information on the regulatory status of assigned products.
• Ensure proper use of the Artwork Management System to support efficient artwork creation and revision processes.
• Implement and maintain regulatory databases and systems in compliance with local requirements and internal standards.
• Maintain complete, accurate, and up-to-date regulatory files and archives.
• Contribute to the development, implementation, and continuous improvement of SOPs to ensure compliance with applicable regulations.
• Support the implementation of updated regulatory documentation in alignment with agency requirements and internal policies.
• Address regulatory process-related issues, ensuring timely resolution.
• Conduct investigations in accordance with our company standards and local procedures.
• Collaborate closely with local teams on key regulatory activities, including Quality Notifications, GMP inspections, vaccine release documentation, and Annual Product Reviews.

Labeling and Artwork

• Ensure the timely availability of packaging materials, including package leaflets and other artwork, in compliance with Artwork Management procedures and established timelines.

Cross-functional Activities

• Coordinate timely and appropriate actions related to deletions, divestitures, and acquisitions.
• Participate in subsidiary product and launch teams, providing regulatory guidance.

Regulatory Policy & Environment

• Monitor and evaluate new and emerging regulations, as well as proposed changes, assessing their potential impact on business and operations.
• As required, Represent the company in task forces organized by the pharmaceutical industry and regulatory agencies, contributing to policy discussions and regulatory strategy.

Qualifications, Skills & Experience

• Degree in Pharmacy, Life Sciences, or a related field, or equivalent qualification.
• Minimum of 8 years of experience in a Registration Department or equivalent role, including interactions with COFEPRIS.
• Strong knowledge of local legislation, procedures, and guidelines governing pharmaceutical products.
• Excellent verbal and written communication skills.
• Strong organizational and planning abilities.
• Experience in Oncology is required, Biological, Biotechnological, small molecules, etc.
• High attention to detail, adaptability, and the ability to manage multiple priorities under tight deadlines.
• Disciplined, proactive, and able to coordinate tasks effectively across teams.
• Ability to navigate complex regulatory environments with diplomacy and assertiveness when engaging with internal and external stakeholders.
• Proficiency in English.
• Client-oriented mindset aligned with our company´s leadership vision.
• Focus on results, strategic planning, accountability, and execution excellence.

Required Skills

• Adaptability
• Audits Compliance
• Detail-Oriented
• Drug Regulatory Affairs
• Employee Training Programs
• Global Communications
• Pharmaceutical Regulatory Affairs
• Pharmacovigilance
• Process Improvements
• Project Management
• Regulatory Affairs Management
• Regulatory Compliance
• Regulatory Operations
• Regulatory Strategy Development
• Regulatory Submissions

Search Firm Representatives Please Read Carefully

Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.

Employee Status

Regular

Relocation

No relocation

VISA Sponsorship

No

Travel Requirements

No Travel Required

Flexible Work Arrangements

Hybrid

Shift

Not Indicated

Valid Driving License

No

Hazardous Material(s)

na

Job Posting End Date

• A job posting is effective until 11 59 59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.

Requisition ID R423991