Fenixfarma is seeking a Regulatory Affairs Coordinator to join our team in Polanco, Mexico City. This full-time, on-site position and is available for immediate start. The Regulatory Affairs Coordinator will be responsible for preparing and maintaining regulatory documentation, ensuring compliance with local and international regulatory requirements, coordinating regulatory submissions, and collaborating with cross-functional teams to support regulatory needs. Experience in assembling drug product and medical device dossiers is essential for this role; experience with government tenders is a plus.
**Responsibilities**:
Prepare and maintain regulatory documentation, including assembling drug product and medical device dossiers
Ensure compliance with local and international regulatory requirements
Coordinate regulatory submissions to relevant health authorities
Collaborate with cross-functional teams to support regulatory needs
**Qualifications**:




Expertise in regulatory documentation, submissions, and compliance requirements
Proven experience in regulatory affairs
Strong attention to detail and organizational skills
Excellent written and verbal communication skills in Spanish and English
Bachelor’s degree in Pharmacy, Biology, Chemistry, or a related field
Ability to work independently and collaboratively
Experience assembling drug product and medical device dossiers (essential)
Experience with government tenders (a plus)
Pharmaceutical industry experience (a plus)
Pay: $10,000.00 - $15,000.00 per month
**Experience**:
- Regulatory Affairs : 1 year (preferred)
**Language**:
- English (preferred)
Work Location: In person
Expected Start Date: 11/05/2025

📌 Regulatory Affairs Coordinator (Full-time, On-site) (Polanco)
🏢 Fenixfarma Mexico City, Mexico
📍 Polanco