Summer Internship - Biomedical Engineering

This position will be full time onsite at our Cambridge, MA office

Dates: June 9, 2025 – August 15, 2025 (10 weeks)

As a Vericel intern, you will be placed on project(s) under the guidance of an experienced professional, and work along subject matter experts who are invested in your career and academic growth.  We will ensure you have opportunities to build your network, learn about our organization and join us for fun events. 

The selected interns will present their final projects to the leadership team during their final week.

Process Comparison & Analysis Internship

This internship provides a unique opportunity to contribute to Vericel's cutting-edge cell therapy manufacturing processes. You will play a crucial role in analyzing and improving the alignment between our process control strategies, electronic batch records, and actual work practices. This analysis will help identify potential gaps and inconsistencies, ultimately enhancing the efficiency and quality of our cell therapy products.

Key Responsibilities

• Process Observation & Familiarization: Observe and actively engage with Operations in Epicel manufacturing and testing processes to gain a comprehensive understanding of current workflows.
• Data Collection & Analysis: Collaborate with R&D to develop a robust matrix comparing the Epicel Process Control Strategy (PCS) with electronic batch record process instructions (eBR PIs), contingency paper batch records, and observed work practices.
• Gap Identification & Documentation: Meticulously document and analyze findings, identifying any discrepancies or inconsistencies between the documented procedures and actual operations.
• Technical Report & Presentation: Prepare a comprehensive technical report summarizing your findings, including data analysis, observations, and recommendations for improvement. Deliver a concise and impactful presentation to share your insights with key stakeholders.
• Gowning Qualification: Successfully complete gowning qualification requirements for safe and compliant access to cleanroom environments.
• Continuous Improvement: Proactively identify areas for process optimization and contribute to the continuous improvement of manufacturing operations.

Qualifications:

• Impending Bachelor of Science degree in a relevant field (e.g., Biology, Chemistry/Biochemistry, Chemical Engineering, Biomedical Engineering)
• Rising Junior/Senior status
• Prior experience with mammalian cell culture or other biopharmaceutical manufacturing techniques is preferred
• Strong analytical and problem-solving skills, proficiency in data analysis and interpretation, strong attention to detail.
• Excellent written and verbal communication skills, ability to clearly and concisely present complex information to diverse audiences.
• Strong teamwork and collaboration skills, ability to work effectively with cross-functional teams (R&D, Operations, Quality).
• Currently enrolled in an accredited college or university
• Permanent U.S. Work Authorization