Manufacturing & Quality Assurance Intern

Manufacturing & Quality Assurance Intern

📍 Location: Holliston, MA → In-Person
⏳ Duration: May 12th - August 22nd, 2025 (Full-Time, 9 AM - 5 PM)
💰 Compensation: Summer Stipend - ($2-4k based on time and performance). 

About the Role:

NeuroSync is seeking a Manufacturing & Quality Assurance Intern to assist in building and testing new medical device units while supporting data collection and report generation for our clinical comprehensive and general wellness reports. This internship offers hands-on experience in medical device manufacturing, quality control, and data analysis, providing valuable exposure to a fast-paced med-tech environment.

Key Responsibilities:

• Assist in the manufacturing and assembly of new medical device units, ensuring quality and precision.
• Support quality assurance testing, including functional and performance checks.
• Collect and analyze clinical and operational data to contribute to our comprehensive and general wellness reports.
• Help develop standard operating procedures (SOPs) for manufacturing and quality control.
• Assist in troubleshooting and resolving manufacturing defects or inconsistencies.
• Maintain detailed documentation of production processes, test results, and quality control measures.
• Collaborate with R&D, regulatory, and clinical teams to improve product design and ensure compliance with FDA, ISO, and other regulatory standards.
• Contribute to process improvement initiatives to enhance efficiency and product reliability.

Required Skills & Qualifications:

✅ Currently pursuing a Bachelor’s degree in Mechanical Engineering, Biomedical Engineering, Manufacturing Engineering, or a related field.
✅ Hands-on experience with mechanical assembly, technical troubleshooting, or laboratory testing (through coursework, projects, or prior internships).
✅ Strong analytical skills with proficiency in data collection, statistical analysis, and report generation (Excel, Python, Power BI, or similar tools preferred).
✅ Understanding of quality control principles and regulatory standards (ISO 13485, FDA guidelines a plus).
✅ Ability to read and interpret technical drawings, schematics, and product specifications.
✅ Detail-oriented with strong problem-solving and organizational skills.
✅ Excellent communication and documentation skills.

What You’ll Gain:

• Hands-on experience in medical device manufacturing and quality assurance.
• Exposure to clinical data analysis and reporting in a med-tech environment.
• Mentorship and collaboration with industry professionals in engineering and regulatory affairs.
• The opportunity to work on cutting-edge technology that advances neurological care.