What you'll be doing
- Contribute to device design and development, risk management, and human factors engineering activities according to relevant regulations and industry standards, including 21 CFR 820, ISO 13485, EU Medical Device Regulation, ISO 14971, and IEC 62366.
- Support medical device and combination product development on internal programs and activities with external device suppliers and development partners.
- Develop and qualify device test methods and author SOPs.
- Perform drug-device compatibility studies and device safety and functionality testing to support device feasibility studies, engineering assessments, and design verification.
- Author technical protocols and reports, including documents for project Design History Files.
- It is imperative that REGENXBIO employees embody our core values by working collaboratively, building strong relationships, and using clear communication to meet shared objectives.
- This role requires travel up to 10% of the time.
We set our employees up for success. To be successful in this role and help us achieve our goals, we are looking for someone with the following skills and qualifications:
- The ideal candidate will have a Bachelor’s or Master’s degree in a relevant engineering/scientific discipline.
- For Device Engineer I, the ideal candidate will have a Bachelor’s degree and up to 2 years of direct, relevant experience.
- For Device Engineer II, the ideal candidate will have a Bachelor’s degree with 2 to 5 years of direct, relevant experience or a Master’s degree and up to 2 years of direct, relevant experience.
- For Device Engineer III, the ideal candidate will have a Bachelor’s degree with 5 to 8 years, or a Master’s Degree with 2 to 5 years of direct, relevant experience.
- Able to independently plan and perform experiments that support scientific/engineering activities and project goals.
- Able to interpret data, draw conclusions, and recommend next steps.
- Able to effectively communicate information and results in the appropriate format (i.e., lab notebooks, presentations, reports, etc.).
- Familiarity with Design Controls, Risk Management, and Human Factors Engineering for medical devices and combination products is preferred.
- Ideally has an understanding of drug-device interactions.
- Must be able to work collaboratively and effectively as part of a team.
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What We Do
REGENXBIO is a leading biotechnology company focused on the development, commercialization and licensing of recombinant adeno‐associated virus (AAV) gene therapy. REGENXBIO's NAV® Technology Platform, a proprietary AAV gene delivery platform, consists of exclusive rights to more than 100 novel AAV vectors, including AAV7, AAV8, AAV9 and AAVrh10. REGENXBIO's mission is to transform the lives of patients suffering from severe diseases with significant unmet medical need by developing and commercializing in vivo gene therapy products based on REGENXBIO's NAV Technology Platform. REGENXBIO seeks to accomplish this mission through a combination of internal development efforts and third‐party NAV Technology Platform licensees.


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