**Work Schedule**
Standard (Mon-Fri)
**Environmental Conditions**
Office
- Acts as liaison with internal stakeholders in the provision of these services.
- Works with the Regulatory Affairs Management to perform the day to day operational aspects of the Department such as: assessment of regulatory documents, preparation and assembly of general regulatory submissions, QC review of the final submission package.
- Interfaces with PPD project teams and Health Authorities regarding regulatory strategy/submission activities.
- Develops and maintains a cooperative working relationship with Project Managers and project team members for assigned projects.
- Advises and directs project team as to their responsibilities relative to regulatory strategy/submission activities.
- Acts as a key liaison between Regulatory Affairs Department and project team for assigned projects.
Education and Experience:
- Bachelor's Degree; degree in Pharmacy or Life Science is an advantage
- Previous regulatory experience, or combination of higher education/less experience or substitution of equivalent relevant work experience will be considered

📌 Regulatory Affairs Specialist Ii (México)
🏢 Thermo Fisher Scientific
📍 México