Device Engineer I/II/III

REGENXBIO; Rockville (MD); On-site; USD 73,000 - 140,000; Full time

Benefits offered by this job

Market-competitive base salary

Annual performance-based bonus program

Stock grants at all levels

Health, dental, and vision insurance

Retirement plan with 401(k) match

Summer hours

Job summary

REGENXBIO is searching for a Device Engineer to join their team focused on developing drug delivery systems for AAV gene therapy products. The role involves design and development, risk assessments, and ensuring compliance with regulations while collaborating with cross-functional teams. Successful candidates will have a strong engineering background, effective communication skills, and the ability to tackle complex problems independently.

Qualifications

• Relevant engineering/scientific degree required.
• Experience ranges from 0-8 years depending on the level.
• Familiarity with Design Controls and Risk Management preferred.

Responsibilities

• Contribute to device design, feasibility, and human factors engineering.
• Conduct drug-device compatibility studies for feasibility and verification.
• Author technical documents including design history files.

Skills

Ability to independently plan and perform experiments

Data interpretation and recommendation skills

Collaborative teamwork

Clear communication

Understanding of drug-device interactions

Education

Bachelor’s or Master’s degree in relevant engineering/scientific discipline

Job description

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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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