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EMed Summer Internship - Quality & Regulatory Intern

Job in Miami, Miami-Dade County, Florida, 33132, USA
Listing for: eMed, LLC
Seasonal/Temporary, Apprenticeship/Internship position
Listed on 2026-02-17
Job specializations:
  • Healthcare
    Healthcare Compliance
Salary/Wage Range or Industry Benchmark: 15 USD Hourly USD 15.00 HOUR
Job Description & How to Apply Below
Position: 2026 eMed Summer Internship - Quality & Regulatory Intern

eMed is seeking a high-energy, detail-oriented Quality & Regulatory Intern to join our team. At eMed, we are redefining healthcare delivery through technology. This role offers a unique opportunity to learn how a digital health company maintains institutional-grade compliance while operating at the speed of a tech startup. You will support the team in ensuring our products, research, and clinical operations meet the highest standards of safety, privacy, and regulatory rigor.

Key Responsibilities
  • Quality Management System (QMS) Maintenance:
    Assist in the administration of the eMed QMS. This includes managing document control, updating Standard Operating Procedures (SOPs), and ensuring version history accuracy across all departments.
  • Regulatory Submissions & Tracking:
    Support the preparation and filing of regulatory submissions (IRB, FDA, or state-level licensing). Maintain a centralized "Regulatory Calendar" to track expiration dates and renewal milestones.
  • Audit Support & Internal Compliance:
    Assist in conducting internal "spot-check" audits to ensure departmental adherence to HIPAA, SOC2, and internal Quality policies.
  • Marketing & Communications Compliance:
    Review external-facing materials (ads, landing pages, and patient instructions) to ensure they align with approved regulatory claims and clinical protocols.
  • Regulatory Intelligence:
    Monitor and summarize updates from the FDA, FTC, and state medical boards. Help the team assess how new digital health guidelines impact eMed’s current and future product roadmap.
  • Documentation & Reporting:
    Help maintain the "Source of Truth" for all clinical and technical specifications, ensuring that product changes are reflected in our regulatory filings.
Required Qualifications
  • Currently pursuing a degree (Junior/Senior or Graduate level) in Regulatory Affairs, Healthcare Administration, Biomedical Engineering, Law, or a related field.
  • A foundational understanding of HIPAA and GCP (Good Clinical Practice) is preferred.
  • Meticulous attention to detail—you are the person who catches the typo in a 50-page document.
  • Strong communication skills with the ability to simplify complex regulatory requirements for non-technical stakeholders.
  • A "Swiss Army Knife" mindset:
    Comfortable moving between a legal document, a marketing review, and a data security audit.
What You’ll Learn
  • Healthcare Operations at Scale:
    How a telehealth company manages quality across thousands of monthly patient interactions.
  • Risk Management:

    How to identify and mitigate regulatory risks in a fast-evolving digital landscape.
  • Cross-Functional Collaboration:

    How Quality and Regulatory teams partner with Engineering, Marketing, and Clinical teams to launch new products safely.
  • Benefits

    • Competitive hourly pay: $15.00/hour

    • Onsite catered breakfast, lunch, and snacks

    • Real-world experience in a rapidly scaling health-tech organization

    • Exposure to executive leadership and cross-functional teams

    Position Requirements
    Less than 1 Year work experience
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