Regulatory Affairs Trainee: Launch Your Compliance Career

Haleon plc.; Ciudad de México; Sur place; MXN 180 000 - 240 000; Plein temps

Résumé du poste

Haleon plc invites applications for a Regulatory Affairs Trainee to execute and coordinate activities related to regulatory submissions for medicines, medical devices, cosmetics and dietary supplements. You will liaise with multiple business units such as Pharmacovigilance, Manufacturing, Marketing and Supply to ensure timely submissions to COFEPRIS and accurate record-keeping.

The role emphasizes data management, report generation, and metric tracking.

Qualifications

• Entry-level role suitable for recent graduates
• Bachelor's degree in chemistry, pharmacy, biology or related scientific field
• Strong problem-solving and attention to detail
• Clear communication across multiple areas and stakeholders
• Good command of Excel, Word and PowerPoint; intermediate-advanced English

Responsabilités

• Coordinate submissions and receptions of regulatory processes with COFEPRIS and relevant areas
• Support drafting dossiers for advertising and modifications for medical devices, pharmaceuticals, dietary supplements, cosmetics
• Assist in internal corrections for devices and drugs
• Maintain regulatory databases and product registrations
• Support review of artwork and updates on platforms like Veeva Regulatory/Promotion
• Prepare regulatory reports and metrics
• Handle procurement orders for regulatory services and follow up on invoices
• Follow up with pharmaceutical chambers on regulatory filings

Connaissances

Entry Level

Science degree

Chemist

Pharmacist

Biologist

Microbiologist

Excel

Word

PowerPoint

English

Formation

Bachelor's degree in a scientific field

Outils

Veeva

Description du poste

Haleon plc invites applications for a Regulatory Affairs Trainee to execute and coordinate activities related to regulatory submissions for medicines, medical devices, cosmetics and dietary supplements. You will liaise with multiple business units such as Pharmacovigilance, Manufacturing, Marketing and Supply to ensure timely submissions to COFEPRIS and accurate record-keeping.

The role emphasizes data management, report generation, and metric tracking.