About the job
Cresilon® is an innovative biotechnology company located in Brooklyn, dedicated to developing, manufacturing, and marketing advanced hemostatic medical devices powered by our proprietary hydrogel technology. Our groundbreaking plant-based solutions have transformed the standard of care by effectively halting traumatic and surgical bleeding within seconds, eliminating the need for prolonged manual pressure. Our product lines cater to both veterinary and human medical applications, aiming to save lives across various domains. Discover more about us at www.cresilon.com.
This summer, Cresilon is excited to welcome interns from diverse academic backgrounds to provide them with invaluable industry exposure.
We offer both technical and non-technical internship opportunities, each centered around specific projects. All interns will gain insights into various aspects of the biotechnology industry, regardless of their specific focus. The internship spans 10 weeks onsite, commencing on June 1, 2026. Interns will receive a fixed compensation of $30.00 per hour for 40 hours a week, with part-time positions also available. The application window closes on February 27, 2026.
We have ten distinct internship categories available. Please indicate your Top 2 choices in your cover letter:
1. Manufacturing Operations and Supply Chain
Interns will assist with optimization in supply chain processes, production planning, logistics, and the development of Standard Operating Procedures (SOPs) and batch records. Opportunities for compensated travel to industry conferences may be available.
2. Quality Assurance
Interns will contribute to establishing the Quality Management System, crucial for meeting Cresilon's quality and regulatory standards. They will help maintain the central document control system and ensure compliance with OSHA requirements. Compensated travel to conferences may also be available.
3. Quality Operations & Compliance
Interns will support the Quality Operations and Compliance department by helping to maintain and enhance the Quality Management System (QMS). This will provide valuable exposure to ISO 13485 and FDA 21 CFR 820 requirements, while assisting with daily compliance tasks and improving departmental efficiency.

