Regulatory Affairs Specialist- Temporal (1 year)

Novartis; Ciudad de México; Presencial; MXN 750,000 - 1,000,000; Jornada completa

Descripción de la vacante

A leading pharmaceutical company in Mexico City is seeking a professional to manage global regulatory submission projects. The role includes ensuring compliance with regulatory requirements, maintaining documentation systems, and providing strategic input for global products. Candidates should possess strong skills in data analysis, documentation management, and clinical studies. Experience in regulatory compliance is essential, along with the ability to work across diverse teams.

Formación

• Experience in managing global regulatory submission projects.
• Strong understanding of regulatory agency requirements.
• Ability to communicate and enforce documentation standards.

Responsabilidades

• Manage global regulatory submission projects.
• Provide technical and regulatory strategy support.
• Ensure adherence to company policies and guidelines.

Conocimientos

Clinical Study Reports

Data Analysis

Documentation Management

Lifesciences

Operational Excellence

Regulatory Compliance

Descripción del empleo

Job Description Summary

Ensures a controlled documentation system, record retention, and information services including electronic records retention processes in accordance with regulatory requirements. Ensures compliance to the requirements from regulatory agencies. Maintains the technical and non-technical documentation change system. Assures procedures are in place to classify and maintain records. Interprets & enforces all documentation formatting, standards, policies, and operating procedure requirements. May identify submission components, communicate documentation standards and coordinate assembly of regulatory dossiers. May analyze and evaluate data, extract pertinent information, prepare information abstracts and executive summaries of material searched. May maintain extensive knowledge of product information and continuous contacts with local, regional, and divisional customers.

Job Description

Major accountabilities

• Manages medium to small level global regulatory submission projects.
• Provide submission and contribute to the technical related regulatory strategy, intelligence and knowledge required to develop, register, and maintain global products.
• Contribute to strategic and technical input /support to drive implementation of global systems, tools and processes to support global development projects and/or marketed products.
• Frequent internal company and external contacts.
• Represents organization on specific projects -Works on problems of moderate scope where analysis of situations or data requires a review of a variety of factors.
• Reporting of technical complaints / adverse events / special case scenarios related to Novartis products within 24 hours of receipt -Distribution of marketing samples (where applicable)

Key performance indicators

• Adherence to Novartis policy and guidelines -Project & stakeholder feedback

Work Experience

• Cross Cultural Experience.
• Functional Breadth.
• Collaborating across boundaries.
• Operations Management and Execution.
• Project Management.

Skills

• Clinical Study Reports.
• Data Analysis.
• Documentation Management.
• Lifesciences.
• Operational Excellence.
• Regulatory Compliance.

Languages

• English.

Skills Desired

Clinical Study Reports, Data Analysis, Documentation Management, Lifesciences, Operational Excellence, Regulatory Compliance