What are the responsibilities and job description for the Research And Development Engineer position at Elutia?
Position Overview :
The R&D Engineer at Elutia is responsible for designing and developing biological-based medical devices, specializing in drug / device combination products according to industry standards. This role encompasses overseeing the entire development process, from initial concept through to commercialization. The R&D Engineer leads prototype and pilot production, develops and executes test methods, and collaborates with cross-functional teams to advance Elutia's product pipeline. They ensure seamless product development and facilitate tech transfer for successful clinical and commercial use by applying critical thinking skills to solve technical issues. Additionally, the R&D Engineer contributes to the intellectual property portfolio and ensures compliance with regulatory requirements to gain product approvals and support product lifecycle management.
The successful candidate will work onsite at the Company’s Gaithersburg, MD facility
Essential Duties & Responsibilities
- Designing and characterizing biological matrices (decellularized ECM, collage, polymer) and drug / device combination products according to industry standards.
- Developing drug coating and alternative drug delivery methods for sustained or extended release products.
- Developing and executing test methods to support exploratory research and introduce new techniques.
- Supporting prototype and pilot production of new products in collaboration with Manufacturing and Quality Control Systems.
- Applying critical thinking skills to product development and design, troubleshooting technical issues in the lab.
- Establishing testing plans and ensuring timely completion of technical deliverables.
- Leading project development and overseeing tech transfer to manufacturing for clinical and commercial use.
- Utilizing quantitative data analysis skills to inform decision-making processes and effectively communicate results.
- Contributing to the intellectual property portfolio through innovative solutions.
- Supporting a successful and efficient regulatory approval process, including 510(k) or PMA pathways, to ensure compliance with FDA requirements.
- Maintaining accurate and timely records of development activities as per written procedures.
- Collaborating across multiple functions, including Marketing, Regulatory Affairs, Quality, and Clinical Operation
Education & Experience
