Evergen

About the Company

Evergen is a leading Contract Development and Manufacturing Organization (CDMO) pushing the boundaries of innovation and tissue engineering to meet patient needs in regenerative medicine. We are expert partners to Original Equipment Manufacturers (OEMs), working with them to identify clinical problems and develop customized solutions that promote healing, accelerate recovery, and help prevent complications. Using our extensive portfolio of biological materials, we focus on specialized clinical segments, including plastic and reconstructive surgery, sports medicine and orthopedics, cardiac, and neurosurgery. Our Mission is to enhance patients' lives by creating the best clinical outcomes through innovative, high-quality medical solutions.

Listed Jobs

Company Name

Evergen

Job Title

Intern - Research & Development

Job Description

Job Title: Intern – Research & Development **Role Summary** Assists the R&D team in designing, developing, and testing new and improved implant prototypes and processes. Conducts laboratory experiments, analyzes data, and prepares technical documentation and presentations. Supports process optimization and collaborates with cross‑functional teams to deliver high‑quality research outcomes. **Expectations** - Commit up to 20 hours per week during normal business hours. - Be a 3rd‑ or 4th‑year undergraduate student or a graduate student in Biomedical Engineering, Materials Science, or a related scientific/engineering discipline. - Exhibit strong initiative, meticulousness, and the ability to work independently and collaboratively. - Demonstrate willingness to learn surgical procedure basics and apply knowledge to innovative solutions. **Key Responsibilities** - Design and fabricate prototype implants and devise/improve processing methods. - Plan, execute, and troubleshoot laboratory experiments. - Collect and analyze experimental data using sound statistical techniques; draw scientifically valid conclusions. - Draft protocols, reports, SOPs, and other technical documents in accordance with Good Documentation Practices. - Consult with internal and external scientific communities to stay current on best practices. - Create or recommend tools and job aids to support new product manufacture. - Assist senior staff on routine scientific tasks that are integral to larger projects. - Participate in safety and quality protocols; lift up to 25 lb as needed. **Required Skills** - Ability to independently design, conduct, and analyze experiments. - Proficient written and verbal communication; capable of preparing clear technical documentation. - Strong organizational and time‑management skills. - Team player with interpersonal skills to collaborate across functions. - Problem‑solving skills; able to resolve technical issues within scope of academic knowledge. **Required Education & Certifications** - Pursuing a bachelor’s or master’s degree in Biomedical Engineering, Materials Science, or a related field; senior undergraduate or graduate student status. - No specific certifications required. ---

Alachua, United states

On site

Fresher

29-10-2025