Regulatory Affairs Specialist 2

As a Regulatory Affairs Specialist, you will be integral to our mission of facilitating the timely approval and distribution of critical medical products.

Your key responsibilities will include:

• Coordinating and documenting internal regulatory processes such as document inspections, license renewals, and registrations.
• Compiling and preparing submission materials for customers and regulatory agencies.
• Managing document preparation, information management, and file maintenance.
• Collaborating across multiple departments to create comprehensive submission dossiers for product licensing and registration in various countries.
• Establishing direct contact with customers to ensure seamless communication and compliance.

Important eligibility and role requirements:

• This role is not eligible for visa sponsorship and does not include a relocation package.
• Prospects must be currently located in Mexico, Central America and Puerto Rico.
• Must be fluent in English and Spanish

1. Make an Impact: Contribute to the global distribution of life-saving products and improve health outcomes worldwide.

2. Professional Growth: Benefit from continuous training and development opportunities to advance your career in regulatory affairs.

3. Collaborative Culture: Work in a supportive and inclusive environment that values diversity and teamwork.

4. Innovation: Be part of a forward-thinking company that embraces innovation to stay ahead in the regulatory field.

5. Competitive Benefits: Enjoy a comprehensive benefits package, including health insurance, retirement plans, and flexible working hours.

You can submit your resume here using our form or send it directly to careers@rebexa.com.

For a detailed job description, click the link below to view a PDF version.

Rebexa Group is an equal-opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employee