Device Engineer I/II/III
regenxbioDerwood, MD
$75,000 per year
Apply nowDevice Engineer I/II/III
L5
regenxbioDerwood, MDyesterday
$75,000 per year
Industries
Research and Development in Biotechnology (except Nanobiotechnology)Electromedical and Electrotherapeutic Apparatus ManufacturingSurgical and Medical Instrument ManufacturingGet AI-powered advice on this job and more exclusive features.
Who We Are:
REGENXBIO is an exceptional place to work. You'll have the opportunity to collaborate with some of the best and the brightest people, touch amazing science, and be a part of extraordinary plans. Our core values: Trust, Accountability, Perseverance, and Innovation drive everything we do. We aim to bring these values to life every day with all that we do, and we believe that what we do matters - to patients, to their families, and to their communities. As our Device Engineer, you will be part of a team responsible for the development of drug delivery systems for recombinant adeno-associated virus (AAV) gene therapy products. You will support a portfolio containing delivery technologies intended for localized delivery, including ocular and intrathecal routes of administration, and for systemic intravenous delivery. In this role, you will contribute to device feasibility evaluations, design and development, risk management, and human factors engineering. You will work independently and as a part of cross-functional teams on assigned projects, prioritize projects to meet departmental and organizational goals, and communicate results in technical reports and presentations.
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 Why You Should Apply By joining REGENXBIO, you will have the opportunity to be a part of a growing company and incredible team passionate about developing novel AAV gene therapy products to our patients. In addition, professional development is important to us. By joining our team, you’ll have the opportunity to be exposed to challenging projects and development resources to help you grow personally and professionally. We are proud to offer a comprehensive rewards package which includes a market-competitive base salary, an annual performance-based bonus program, stock grants at all levels, and benefits such as health, dental, and vision insurance, retirement plan with 401(k) match, summer hours, and more! The estimated compensation range for this role is $73,000 to $140,000 annually, depending on level. The actual salary offered to the final candidate depends on a number of factors such as relevant work experience, skills, education, and years of experience.
Seniority level Seniority level Not Applicable
Employment type Employment type Full-time
Job function Job function Quality Assurance
Industries Hospitality, Food and Beverage Services, and Retail
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Level
SeniorL5
Salary
$75,000 per year
Location
Derwood, MD
Occupation
Bioengineers and Biomedical Engineers
Industry
Research and Development in Biotechnology (except Nanobiotechnology)
Posted
yesterday
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