Summer Intern – Combination Product Development

About the role

At Insmed, every moment and every patient counts — and so does every person who joins in. As a global biopharmaceutical company dedicated to transforming the lives of patients with serious and rare diseases, you’ll be part of a community that prioritizes the human experience, celebrates curiosity, and values every person’s contributions to meaningful progress. That commitment has earned us recognition as Science magazine’s No. 1 Top Employer for five consecutive years, certification as a Great Place to Work® in the U.S., and a place on The Sunday Times Best Places to Work list in the UK. For patients, for each other, and for the future of science, we’re in. Are you? We’re looking for a Combination Product Development Intern on the Manufacturing team to help us expand what’s possible for patients with serious diseases. The Insmed Summer Internship Program is designed to give you more than just a glimpse into the pharmaceutical industry—it’s a chance to make a real impact. Over the course of the summer, you’ll gain hands-on experience, contribute to meaningful team projects, and learn directly from skilled professionals who are invested in your growth. Our 2027 Summer Intern program is a full-time (40 hours per week), 12-week, paid internship. The internship may present opportunities for rotational assignments within the function, and the intern will be assigned goals and objectives that will support the strategic business plan of the company. This is a hybrid role based out of our Bridgewater, New Jersey office. You’ll work remotely most of the time, with in-person collaboration when it matters most.

Responsibilities

• Gain hands-on experience working across multiple combination product programs at different stages of the product development lifecycle, making direct contributions to deliverables that help bring life-changing therapies to patients with serious diseases.
• Assist with Design Verification activities in support of regulatory submissions.
• Provide support in Risk Management and Design Controls, assisting with design control activities and associated deliverables across relevant project areas.
• Apply systematic problem-solving methodologies to identify, communicate, and resolve quality issues.
• Support Post-Market Surveillance activities, including complaint handling, investigation, and root cause analysis.
• Participate in potential rotational assignments within the function.

Requirements

You must be a current student pursuing a Bachelor’s or Master’s degree in Biomedical, Mechanical, or Chemical Engineering.

Qualifications

Nice to have (but not required): experience in medical devices, testing, data analysis, and technical writing.

Skills

• Detail-oriented with strong organizational and time management skills
• Effective written and verbal communication skills
• Able to analyze data, identify trends, and summarize key takeaways
• Comfortable working with digital tools and platforms
• Eager to work collaboratively in a team environment

Benefits

• Paid company holidays
• Hands-on learning in real-world projects
• Networking opportunities with leaders and social events with peers
• Mentorship and professional development
• A final presentation to celebrate your contributions
• Access to office amenities for those who are not remote

Pay

Pay range: $20.00‑35.00 per hour.

Schedule

Full‑time (40 hours per week), 12‑week internship.