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Regulatory affairs consultant (hybrid) | (jzd-108)

San Miguel Topilejo, D.F.
ClinChoice
Publicada el 24 septiembre
Descripción

Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring? Our team says it’s the best of both worlds….

Clin Choice is searching for a Regulatory Affairs Consultant till Dec’2025 with (possibility of extension into 2026) to join one of our clients.

Hybrid Model: 2 days a week

Location: S.A. de C.V. Boulevard Adolfo Ruiz Cortines No. 3720, Torre 1 - Piso 3, Col. Jardines del Pedregal, C.P. 01900, Álvaro Obregón, Ciudad de México, México.

Responsibilities:

- Preparation, compilation, and coordination of high-quality regulatory submissions for new product launches, product updates, and throughout product lifecycle.
- Ensure that documents to be submitted to health authorities are ready by ensuring quality review is performed before forwarding to client regulatory personnel.
- Research, draft and assemble the documents required to secure export certificates, market specific product applications/ notification and health authority clearances
- Review of artwork changes and associated change controls, including tracking of deliverables.
- Monitoring of new and changing regulatory standards and dissemination of information.
- Support coordination of label change initiation, label reviews and changes in accordance with regional /country review system and procedure.
- Provide regulatory input, review and approval related to change control
- Support product portfolio through execution of legal document activities as required
- Coordination with cross functional teams, manufacturing site and local affiliates for the required information to process the documents
- Search different internal tools for the required information to process the documents.
- Develop and manage regulatory action item tables for country specific requirements
- Mapping, coordination of regulatory inputs and timing end to end for country requirements resulting from legal entity change e.g., documentation required, timelines for registrations/notifications and phase-in of changes to meet compliance requirements
- Communicate internally and monitoring deliverables ensuring country requirements are met by specified timeframes
- Record and publish meeting notes. Incorporate follow-up items to project deliverable tracking, ongoing monitoring, and issue escalation to client local managers.
- Manage regulatory action item (task) tables including mapping, coordination of regulatory inputs, and timing
- Work with client regulatory managers to develop project implementation plans
- Support client regulatory managers in their registration procedure
- Complete market impact assessments
- Generation of databases and checklists for project monitoring
- Support in the creation of product history and archives
- Company systems update

Deliverables:

- Provision of weekly updates (at a minimum) to relevant client regulatory managers
- Ensure regulatory standards and timelines are met
- Plan and track the status of ongoing regulatory projects
- Regulatory action item tables for country specific requirements and importation/ exportation needs for change in legal entity
- Presentation materials for management updates
- Ensuring documents for health authority are submission-ready
- Supporting coordination of label change initiation, label reviews and changes in accordance with regional /country review system and procedure.
- Regulatory input, review and approval related to Change Control

Experience/Qualifications:

- Regulatory professional with formal college or higher education in science related discipline
- Relevant work experience with minimum 2+ years in regulatory affairs
- Individuals must have fluency of English and local language.
- Good understanding of local regulations for OTC,Cosmetics and Medical devices
- Strong working knowledge of Microsoft Word, Excel, Power Point
- Good communication and follow up skills with country regulatory liaisons for clear understanding of country specific needs for registrations, license updates and import/export requirements.

📌 Regulatory Affairs Consultant (Hybrid)
🏢 ClinChoice
📍 San Miguel Topilejo

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