Regulatory Affairs Intern/Co-op

About Us: Pramand, LLC, is a medical device company based in Bedford, MA, focused primarily on PMA as well as 510(k) products. We develop implantable medical devices from novel, proprietary hydrogel materials that improve patient outcomes while lowering the cost of therapy. We self-fund our projects through preclinical development and work with financial partners for clinical development and commercialization. Our portfolio of hydrogel technology positions us to be the leader in creating new hydrogel based medical devices to address unmet medical needs in a range of surgical interventions. We have launched over ten medical device companies based on this unique technology. These companies have generated over $4B in value and have helped over 5 million patients worldwide achieve better outcomes.

Role Title: Regulatory Affairs Intern/Co-op

Hours: Full-time, 40 hours per week, Monday through Friday from 9am-5pm (or 8am-4pm)

Work mode: On-site 4 days a week, Monday-Thursday with flexibility to work remotely on Fridays depending on business needs

Onsite Location(s):  Bedford, MA

Classification: Hourly, Non-Exempt

Employment Type: Internship/Co-op (this is a temporary position is for students only)

Pramand, LLC is looking for a regulatory affairs intern/co-op student interested in medical devices and combination products to work with the regulatory team.

This position could run for the summer or for both summer and fall 2026 depending on student availability.

This role involves assisting in the preliminary review of regulatory documents, supporting submission work (annual reports, supplements and FDA responses) and maintaining up-to-date knowledge of relevant regulations and requirements. 

This internship opportunity is designed to provide hands-on experience and mentorship for an undergraduate or graduate student enrolled in a relevant field of study. This is an onsite position in Bedford, MA reporting to the Principal Regulatory Affairs Specialist. 

Qualifications – Skills and Requirements

• Currently pursuing a degree in a health or scientific discipline, such as PharmD, Pharmacy, Chemistry, Biology, Engineering, or Regulatory Affairs 
• Familiarity with applicable regulations and guidance (US) is a plus but not required 
• Strong attention to detail and ability to review and compile documents for regulatory submissions
• Ability to read, understand, and summarize technical and scientific information
• Excellent computer skills including Microsoft Office applications 
• Ability to work with people at all levels
• Excellent written and verbal communication skills
• Strong organization and time management skills
• Must be able to commute to the office in Bedford, MA