Senior Biomedical Researcher

NeuroWave Systems Inc. is a pioneering medical device manufacturer of an advanced brain monitoring system for use in the operating room, and developer of an autopilot for delivery of anesthesia/sedation for military and civilian applications. Our goal is to revolutionize the standard of care in Anesthesia & Critical Care by providing next generation brain monitoring systems & automated drug-delivery devices to improve patient safety, outcomes and quality of life.

We are looking to fill an IMMEDIATE opening for a Senior Biomedical Researcher with a background in state-of-the-art signal processing techniques / analysis algorithms applied to physiologic signals. We are looking for someone with a strong background in algorithm development and MATLAB, good work ethics and interpersonal skills. The candidate must be detail-oriented, systematic, persistent, driven and willing to work hard. NeuroWave offers a strong salary, health benefits, 401(k) and outstanding personal growth potential.

Job Function:

To actively contribute to conception, development and execution of innovative R&D projects involving new medical devices via advanced signal processing and algorithm development, and to contribute in securing R&D grant funding.

Duties and Responsibilities:

  • Develop and implement novel signal processing / analysis algorithms in MATLAB for patient / subject monitoring and aid in diagnosis / therapy based on physiological signals such as electroencephalogram (EEG).
  • Execute / administer funded R&D programs, both independently and collaboratively. Interface as needed with funding agencies and program officials.
  • Assist in conceiving new ideas within Company’s mission statement and write grant proposals to the NIH, DOD and other funding agencies.
  • Assist with the design and implementation of clinical studies to acquire bio / physiological signals from human subjects for algorithm development and validation.
  • Develop and validate algorithms based on acquired human subjects / clinical data.
  • Perform statistical analysis of acquired and processed data.
  • Develop and maintain regulatory documentation for related clinical studies (Trial Master File and Study Site File) as per current Good Clinical Practice (cGCP).
  • Participate as needed in training, monitoring and audits of clinical sites.
  • Prepare scientific reports and publications. Present at scientific conferences.
  • Provide support for intellectual property protection.
  • Provide support for EU/FDA regulatory submissions.
  • Perform any other related duties as assigned.
  • Travel (incl. international) may be needed.

Education and Skills:

  • MS (or PhD) or equivalent, in biomedical engineering, electrical / computer engineering, or related fields.
  • Theoretical knowledge and practical experience in biomedical research, particularly in advanced signal processing / analysis.
  • Proven track record in conception and implementation of innovative algorithms for extraction of relevant information / features from signals / data.
  • Proficient in programming in MATLAB.
  • Excellent oral/verbal/written communication skills in English.
  • Experience with writing scientific publications.
  • Experience with statistical analysis of data is strongly desired.
  • Experience with writing grant proposals is desired.
  • Experience with analysis of bio / physiological signals is desired.
  • Experience in cGCP and medical device industry regulation is desired.

Please email your cover letter and resume (with salary requirements) to our HR Department at