Senior Specialist Regulatory Affairs (Oncology)

MSD; Ciudad de México; Hybrid; MXN 1,000,000 - 1,800,000; Full time

Benefits offered by this job

Hybrid work arrangement

Job summary

MSD in Mexico City is seeking a Senior Specialist Regulatory Affairs (Oncology) to lead regulatory submissions, lifecycle management, and interactions with COFEPRIS. The role emphasizes strategic regulatory planning and strong collaboration with internal partners.

The ideal candidate will have 8+ years in regulatory affairs, oncology experience, and fluency in English. Hybrid work arrangements and a proactive, detail-oriented mindset are highly valued in this fast-paced environment.

Qualifications

• Degree in Pharmacy, Life Sciences, or related field.
• Minimum of 8 years of experience in a Registration Department or equivalent.
• Experience with COFEPRIS and local regulations.
• Excellent verbal and written communication skills.
• Experience in Oncology is required.
• Strong organizational and planning abilities.
• Ability to manage multiple priorities under tight deadlines.

Responsibilities

• Lead timely submission of New Marketing Authorization (MA) applications.
• Maintain and renew MA authorizations, variations, and post-approval changes.
• Coordinate CMC post-approval changes, labeling and lifecycle management.
• Provide regulatory guidance to cross-functional teams and stakeholders.
• Monitor regulatory requirements and implement SOPs to ensure compliance.
• Support labeling, artwork, and documentation processes for regulatory submissions.
• Collaborate with local teams and regulatory authorities (COFEPRIS).

Skills

Regulatory planning

English proficiency

Cross-functional collaboration

Regulatory strategy

Communication skills

Education

Pharmacy or Life Sciences degree

Job description

Senior Specialist Regulatory Affairs (Oncology)*This site uses cookies to provide you with an optimal user experience. The cookies include Strictly Necessary and Functional cookies to ensure the site operates as intended (language preference, time zone and workload balance). These cookies are first party cookies, end with the session and are exempted from consent. In addition, this site also uses a Google Analytics Cookie to measure and improve the performance of our site. All information these cookies collect is aggregated and therefore anonymous. By clicking on the ‘Accept Cookies’ button, you are accepting this Performance cookie. You may use this site if you click on the ‘Reject Cookies’ button. To revoke your consent of the Performance cookie, clear your cookies within your browser settings.*### Senior Specialist Regulatory Affairs (Oncology)Apply: Hybrid: MEX - Federal District - Mexico City: Full time: Posted Today: End Date: November 13, 2026 (16 days left to apply): R423991Job DescriptionWe 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. **Additional location(s) Compensation Information:****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**Preferred Skills:**Current Employees apply HERECurrent Contingent Workers apply HERE**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:**11/13/2026**\\*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.**Our company is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. The difference between potential and achievement lies in the spark that fuels innovation and inventiveness; this is the space where we have codified our legacy for over a century. Our success is backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare.