Regulatory & Market Access Intern
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At a glance
Requirements
Credentials this posting asks for.
Job overview
Avania is hiring a Regulatory & Market Access Intern. Avania seeks a Medical Device Regulatory Affairs & Quality Intern for a six‑month placement, offering hands‑on experience supporting consulting projects, client deliverables, and strategic marketing initiatives. The intern will work directly with senior consultants, gaining practical insight into medical device regulation, quality systems, and the consulting business while contributing to research, content creation, and internal processes.
Key focus areas include Generate leads and conduct market research, Research emerging medical device companies and consulting opportunities, and Support CRM data entry, client tracking, and outreach efforts.
Important skills include Research, Writing, Analytical Skills, Medical Device Regulation, ISO 13485, and FDA QSR/QMSR.
Skills & qualifications
Skills
Qualifications
Full job description
Avania are Hiring – Regulatory & Market Access Intern
We are seeking, Medical Device Regulatory Affairs & Quality Intern to join the Advisory team for a six-month placement. The roles offer hands-on experience supporting medical device consulting projects, client deliverables, and strategic marketing initiatives. You will work directly with senior consultants to gain practical insight into medical device regulation, quality systems, and the business of consulting.
Key Responsibilities
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Lead Generation & Market Research
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Research emerging medical device companies and consulting opportunities.
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Support CRM data entry, client tracking, and outreach efforts.
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Content Development
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Contribute to creation of medical device regulatory and quality-focused white papers, blogs, and marketing materials.
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Conduct medical device literature and regulatory research to support technical writing.
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Quality & Regulatory Support
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Assist consultants on client work including:
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Support data organization and report preparation for client deliverables.
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Internal Process Support
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Help maintain templates and knowledge management tools.
Qualifications
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Current Northeastern University Master of Science in Regulatory Affairs students with interest in medical devices.
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Strong research, writing, and analytical skills.
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Interest in medical device regulation, ISO 13485, FDA QSR/QMSR, and EU MDR/IVDR.
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Proficient in Microsoft Office and collaborative online tools (SharePoint, Teams, or similar).
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Detail-oriented, self-motivated, and eager to learn in a fast-paced consulting environment.
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Local to either Boston or Toronto campuses
What You’ll Gain
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Exposure to real-world regulatory and quality projects in the medical device industry.
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Experience collaborating with senior consultants and clients across global markets.
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Skill-building in regulatory strategy, QMS development, and technical writing.
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Opportunity to contribute to visible marketing and thought leadership initiatives.
Applicants must be legally authorized to work in the United States at the time of hire. This internship is intended to serve as a pathway to full-time employment. Candidates must have authorization to work in the United States that does not require current or future employer-sponsored visa sponsorship, as sponsorship is not available for this internship or subsequent full-time employment.
We look forward to receiving your application!
Avania - MedTech's trusted Champion
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