About The Position
Avania is hiring a Medical Device Regulatory Affairs & Quality Intern to join the Advisory team for a six-month placement. This role offers hands-on experience supporting medical device consulting projects, client deliverables, and strategic marketing initiatives. The intern will work directly with senior consultants to gain practical insight into medical device regulation, quality systems, and the business of consulting.
Requirements
- Currently pursuing a degree in a relevant field (e.g., Regulatory Affairs, Quality Assurance, Biomedical Engineering, Business, Marketing).
- Strong research and analytical skills.
- Excellent written and verbal communication skills.
- Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint).
- Ability to work independently and as part of a team.
- Detail-oriented with strong organizational skills.
Nice To Haves
- Previous internship experience in the medical device industry.
- Familiarity with CRM software.
- Knowledge of medical device regulations (e.g., FDA, EU MDR).
- Experience with content creation or technical writing.
Responsibilities
- Research emerging medical device companies and consulting opportunities.
- Support CRM data entry, client tracking, and outreach efforts.
- Contribute to the creation of medical device regulatory and quality-focused white papers, blogs, and marketing materials.
- Conduct medical device literature and regulatory research to support technical writing.
- Assist consultants on client work including data organization and report preparation for client deliverables.
- Help maintain templates and knowledge management tools.
Benefits
- Hands-on experience in medical device consulting.
- Direct mentorship from senior consultants.
- Exposure to medical device regulation, quality systems, and business consulting.
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What This Job Offers
Career Level
Intern
Education Level
No Education Listed
