Job Description
Join our dynamic team as an Intern and contribute to vital projects within the organization focusing on government customers' quality standards. This internship offers a unique opportunity to gain hands-on experience in regulatory affairs, interact with industry professionals, and play a crucial role in ensuring compliance with government regulations.
Responsibilities:
Documentation: Track and document all correspondence, including calls and emails, from receipt to closure in the existing tracking system. Work in real-time to capture inquiry-specific information and maintain a comprehensive record.
Written Communication: Support the drafting of written responses to inquiries, coordinating with the FDA for review and approval. Learn effective communication and collaboration with government representatives to ensure appropriate and compliant responses.
Project Coordination: Assist in coordinating efforts with team members, maintaining accurate and timely information. Contribute to project planning, implementation, and issue resolution. Participate in the preparation of project policies and procedures.
Qualifications:
Currently enrolled in a Bachelor's or master’s program
Strong attention to detail and a commitment to accuracy.
Excellent written and verbal communication skills.
Ability to collaborate effectively in a team-oriented environment.
Familiarity with Microsoft Office or Google Workspace.
Interest in regulatory affairs, healthcare, or public health.
Benefits:
Practical experience in regulatory affairs within the healthcare industry.
Networking opportunities with industry professionals and government representatives.
Mentorship from experienced regulatory affairs professionals.
Duration and Compensation:
This is a 12-month internship position with the possibility of extension. Compensation will be provided based on qualifications and experience.