Experienced RA Professional Lifecycle Submissions LATAM

7425-Janssen Cilag Farmaceutica S.A. Legal Entity; Ciudad de Mendoza; Presencial; ARS 90.873.000 - 136.310.000; Jornada completa

Descripción de la vacante

Johnson & Johnson in Argentina is seeking an Experienced Regulatory Affairs Professional for LATAM lifecycle submissions. You will manage end-to-end post-registration activities across multiple LATAM countries, ensuring compliance and timely updates in variations.

Responsibilities include dossier preparation, submission tracking, and interaction with Health Authorities, while coordinating with RA, Supply, CQ, and other stakeholders in a dynamic, global team.

Formación

• Bachelor’s degree in Pharmacy or Biological Sciences is required.
• Approximately 3–4 years of regulatory experience in pharmaceuticals.
• Spanish proficient; English advanced.
• Experience with biological products and labeling updates.

Responsabilidades

• Prepare submission-ready dossiers based on local requirements and J&J standards.
• Ensure timely assessment, submission and approval of life cycle variations.
• Monitor regulatory submissions and approvals.
• Be first point of contact for LCM with local RA colleagues.
• Handle Health Authority queries for LCM submissions with stakeholders.
• Communicate and align with local teams across scope countries.
• Maintain RA databases related to LCM and archive documents.
• Participate in meetings with departments and contribute knowledge.
• Assess impacts of new legislation and implement plans.

Conocimientos

Analytical Reasoning

Brand Research

Business Behavior

Design Thinking

Detail‑Oriented

Industry Analysis

Market Research

Package and Labeling Regulations

Problem Solving

Process Oriented

Product Packaging Design

Project Management

Project Support

Proof Reading Software

Quality Assurance (QA)

Regulatory Affairs Management

Regulatory Compliance

Risk Assessments

Safety‑Oriented

Educación

Bachelor’s degree in Pharmacy or Biological Sciences

Herramientas

RA systems

Descripción del empleo

At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.Learn more at jnj.com. As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.

Job Details

Job Function: Regulatory Affairs Group

Job Sub Function: Regulatory Affairs

Job Category: Professional

All Job Posting Locations: Buenos Aires, Argentina, Las Condes, Santiago, Region Metropolitana de Santiago, Chile, Mexico City, Mexico

Job Description

Johnson & Johnson is recruiting for a Experienced RA Professional Lifecycle Submissions LATAM, to work in Cross‑Regional Operations & Strategy Support (C‑ROSS).

Position summary: This is a Regulatory Affairs professional with local/regional responsibility. The role purpose is to be responsible for the end‑to‑end process execution of regulatory lifecycle management (LCM) in Chile, Argentina, Uruguay, Paraguay, Bolivia, and other LATAM countries, focused on post‑registration process.

Accountability: Execution of the complete LCM regulatory process related to post‑registration (variations) updates. This includes ensuring the accuracy of assessments, dossier preparation, timely submission, and securing approvals, while maintaining compliance with all relevant regulations.

Key Responsibilities

• Prepare submission‑ready dossier based on local requirements and J&J standards and procedures.
• Ensure assessment, submission and approval of life cycle variations in a timely manner.
• Monitoring of Company regulatory submissions/approvals.
• Be first point of contact for LCM with the local Regulatory Affairs colleagues.
• Handle any Health Authority query for LCM submissions with applicable stakeholders, ensuring the robustness of the response.
• Continuous communication, integration and alignment with local team (i.e. RA, Supply, CQ, AW responsible, etc) of the countries in scope.
• Responsible for RA databases related to LCM.
• Archiving all relevant documents from submissions and approvals.
• Participate in meetings with different departments, contributing and adding knowledge.
• Assessment of the impacts of new legislation, risks and opportunities and develop a robust plan for implementing new legislation.

Qualifications

Education: Bachelor’s degree in Pharmacy or Biological Sciences is required.

Competencies

• Strong focus on execution and compliance on submissions/approvals.
• Adaptability to adjust to regulatory changes.
• Effective Communication.
• Analytical and data driven decision making (preferably without supervision).
• One team culture and Collaboration within C‑ROSS and all stakeholders.
• Innovation and Continuous Improvement: skills in problem‑solving, critical analysis, and the ability to identify and implement process improvements.
• Agility and curiosity for continuous learning: Eagerness to learn and expand regulatory knowledge for other countries/clusters

Accountability Experience and Skills

• Required: Approximately of 3-4 years of regulatory experience in pharmaceuticals industry.
• Proactive team player, able to take charge and follow‑through.
• Achievement‑oriented with a high degree of flexibility and ability to adapt to a changing regulatory environment.
• Experience of working in a virtual team and/or global organization.
• Strong in data gathering, and interpretation with proficient use of technology including RA systems.
• Previous experience with biological products and labeling updates is required.

Language

Proficient in Spanish; Advanced English is required.

Required Skills

• Analytical Reasoning
• Brand Research
• Business Behavior
• Design ThinkingDetail‑Oriented
• Industry Analysis
• Market Research
• Package and Labeling Regulations
• Problem Solving
• Process Oriented
• Product Packaging Design
• Project Management
• Project Support
• Proof Reading Software
• Quality Assurance (QA)
• Regulatory Affairs Management
• Regulatory Compliance
• Risk Assessments
• Safety‑Oriented

Preferred Skills

• Analytical Reasoning
• Brand Research
• Business Behavior
• Design Thinking
• Detail‑Oriented
• Industry Analysis
• Market Research
• Package and Labeling Regulations
• Problem Solving
• Process Oriented
• Product Packaging Design
• Project Management
• Project Support
• Proof Reading Software
• Quality Assurance (QA)
• Regulatory Affairs Management
• Regulatory Compliance
• Risk Assessments
• Safety‑Oriented