Systems Engineer

Posted 12 Days Ago
Be an Early Applicant
San Diego, CA
118K-151K Annually
5-7 Years Experience
Biotech
The Role
The Systems Engineer at INOVIO will lead the design and development activities for medical devices, ensuring compliance with FDA and MDDR regulations. Responsibilities include creating user needs requirements, managing system input requirements, maintaining traceability matrix, updating risk management files, V&V planning, ensuring compliance to standards, and collaborating with cross-functional teams. Minimum qualifications include a B.S. degree in an engineering-related field, 5 years of medical device experience, and knowledge of various quality and safety standards.
Summary Generated by Built In

About INOVIO
INOVIO is a biotechnology company focused on developing and commercializing DNA medicines to help treat and protect people from HPV-related diseases, cancer, and infectious diseases. INOVIO’s technology optimizes the design and delivery of innovative DNA medicines that teach the body to manufacture its own disease-fighting tools. For more information, visit www.inovio.com.
Job summary
The Systems Engineer will plan and lead the overall design and development activities relating to the medical device. Define the concept of the device and the design using appropriate standards and input from cross functional teams.
Essential job functions and duties

  • Work with marketing to create the User’s Needs Requirements
  • Create and manage System level input requirements
  • Maintain the Traceability matrix
  • Manage and update the Risk Management File such as System Hazard, DFMEA, SW RISK and URRA analysis
  • Manage the device user manual
  • V&V planning and manage execution
  • Update and maintain the Device Master Record (DMR)
  • Ensure compliance to FDA and MDDR regulations
  • Maintain the device standards list
  • Manage external contractors such as Software vendors
  • Review software documentation
  • Collaborate with cross-functional teams to establish agreement on design implementations
  • Work with legal and quality to bring new external vendors on-board
  • Complete other engineering duties as assigned.

Minimum requirements

  • B.S. degree in Engineering related field.
  • Minimum 5 years of medical device experience.
  • Thorough understanding of ISO13485 quality control and documentation or equivalent standards from other regulated industries.
  • Understanding of Risk Management based on IEC 14971
  • Understanding of IEC 62304 Software life cycle process
  • Understanding of Safety standards such as IEC 60601-1 and ISO 11608 for Needle-based injection systems
  • Solid understanding of design control based on 21CFR820.11

INOVIO offers a variety of competitive compensation & benefits to regular full time INOVIO employees including:

  • 401(K) retirement plan with Corporate Matching
  • Annual Incentives 
  • Medical, Dental, and Vision
  • Generous Paid-time off program and company holidays
  • Hybrid work environment (Depending on the nature of your employment with INOVIO)
  • Physical, Mental, & Financial Wellness Program
  • Company-paid Life Insurance plans
  • Long & Short-Term Disability
  • Flexible Spending accounts for medical and dependent care expenses
  • Employee Discount Perks and so much more…

The annualized base salary range for this role is $118,123 to $150,612 and is bonus eligible. Individual pay decisions ultimately depend on various factors including, but not limited to, relevant experience, knowledge, skills, education, geography, internal equity and alignment with external market data.

Disclaimer

INOVIO Pharmaceuticals, Inc. is committed to a policy of equal employment opportunity. In keeping with our policy, INOVIO will recruit, hire, train and promote into all job titles the most qualified individuals, without regard to race, color, creed, gender, gender identity and expression, religion, marital status, registered domestic partner status, age, national origin or ancestry, military or veteran status, physical or mental disability, medical condition including genetic characteristics, sexual orientation, or any other consideration made unlawful by federal, state, or local laws.

A current US work authorization is required. The above statements are intended to describe the general nature and level of work being performed by people assigned to this job. They are not to be construed as an exhaustive list of all responsibilities, duties, and skills required of personnel so classified. All personnel may be required to perform duties outside of their normal responsibilities from time to time, as needed. INOVIO offers an attractive benefits package and is an equal opportunity employer. 

Important notice to employment businesses/agencies

INOVIO does not accept referrals from employment agencies unless written authorization from the INOVIO Human Resources department has been provided. In the absence of written authorization, any actions undertaken by employment agencies shall be deemed to have been performed without our consent and therefore INOVIO will not be liable for any fees arising from employment agency referrals in respect to current or future position vacancies at INOVIO.

The Company
Plymouth Meeting, PA
298 Employees
On-site Workplace
Year Founded: 1979

What We Do

Inovio is a biotechnology company focused on rapidly bringing to market precisely designed DNA medicines to treat, cure, and protect people from diseases associated with HPV, cancer, and infectious diseases. Inovio is the first and only company to have clinically demonstrated that a DNA medicine can be delivered directly into cells in the body via a proprietary smart device to safely produce a robust immune response to destroy and clear high-risk HPV 16 and 18, which are responsible for 70% of cervical cancer, 90% of anal cancer and 69% of vulvar cancer. In addition to HPV, Inovio’s optimized plasmid design and delivery technology have been demonstrated to consistently activate robust and fully functional T cell and antibody responses against targeted cancers and pathogens. Inovio’s most advanced clinical program, VGX-3100, is in Phase 3 development for the treatment of HPV-related cervical pre-cancer. Also in development are Phase 2 immuno-oncology programs targeting HPV-related cancers, GBM, and prostate cancer, as well as externally funded vaccine development programs in Zika, MERS, Lassa, HIV, and COVID-19. Partners and collaborators include Advaccine, ApolloBio Corporation, AstraZeneca, The Bill & Melinda Gates Foundation, Coalition for Epidemic Preparedness Innovations (CEPI), Defense Advanced Research Projects Agency, GeneOne Life Science, HIV Vaccines Trial Network, Medical CBRN Defense Consortium (MCDC), National Cancer Institute, National Institutes of Health, National Institute of Allergy and Infectious Diseases, Plumbline Life Sciences, Regeneron, Roche/Genentech, University of Pennsylvania, Walter Reed Army Institute of Research, and The Wistar Institute. Inovio also is a proud recipient of 2020 Women on Boards “W” designation recognizing companies with more than 20% women on their board of directors.

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