We use cookies. Find out more about it here. By continuing to browse this site you are agreeing to our use of cookies.
#alert
Back to search results
New

Senior Staff Consultant (BME)

Engineering Systems, Inc. (ESI)
95000.00 To 130000.00 (USD) Annually
life insurance, paid time off, paid holidays, flex time, 401(k)
United States, Georgia, Norcross
Dec 23, 2025

Compensation will be made up of a competitive base salary as well as bonus potential determined by your own individual performance and the performance of the organization overall.

About ESi

Engineering Systems Inc. (ESi) is an engineering and scientific investigation and failure analysis firm. We primarily work with law firms, insurance companies, and manufacturers on small to large-scale projects to answer any technical questions they have. Our projects can entail investigating major transportation accidents, equipment failures, personal injury claims, and damage to residential or commercial structures. The variety and depth of our project work creates a variety of fulfilling roles at ESi.

Some of the benefits we can offer you!

  • Professional Development investment
  • Medical, Dental & Vision
  • Life Insurance/Voluntary Life Insurance/Universal Life Insurance
  • 401k with employer match
  • Merit Bonus
  • Annual Bonus
  • Competitive Salary
  • Flexible Time Off (FTO) - encouraged to take at least 20 days of paid time off/year
  • Career Growth
  • Pet Insurance
  • Work/Life Balance
  • 10 paid holidays (9 standard holidays and 1 floating holiday)
  • Access to Wellbeats - on-demand fitness & well-being videos
  • Wellness Reimbursement
  • 30-minute fitness break available in addition to 1-hour lunch break
  • Business casual dress code and positive working environment
  • Continuing education opportunities

About this Role

Responsible for supporting the planning, directing, and coordinating activities of client projects and assisting senior technical staff to ensure that goals and objectives of the project(s) are accomplished within the prescribed time frame and funding parameters by performing the following duties personally and in coordination with other technical staff.

Key Responsibilities:

  • Conduct field investigations/inspections as assigned.
  • Participate in forensic investigations supporting product liability litigation matters.
  • Assist industrial clients on matters related to medical devices.
  • Perform engineering analysis calculations, testing, and research and apply cutting-edge imaging, experimental, and analytical methods to assess biomaterials, surgical equipment, and medical devices.
  • Assist clients with their new product development endeavors or as part of failure analysis studies, safety and functionality evaluations, or scientific marketing campaigns when their devices are in clinical use.
  • Assist in marketing the group's technical capabilities to clients and the scientific community.
  • Investigate, examine, and simulate the relationships between people and medical devices in specialized fields such as orthopaedics, spine, cardiology, neurology, ophthalmology, biology, and combination devices.
  • Promote the group's technical capabilities to clients and the scientific community, develop new skills, and increase industry exposure through specialization in technical consulting.
  • Assist in writing technical reports, perform research, and present technical material clearly and concisely to clients and team members.
  • Assist in preparing well-developed technical presentations and delivering them clearly and concisely to clients and team members.
  • Master and apply project management best practices to establish, review, and adapt assigned portions of project scopes, schedules, and budgets.
  • Ensure individual project responsibilities are resourced and managed to efficiently and effectively achieve overall project milestones and deliverables within budget constraints.
  • Confer with project leader and personnel to resolve roadblocks on assigned project responsibilities.

Education Requirements:

  • Ph.D. in Bioengineering, Biomedical Engineering, Mechanical Engineering, Electrical Engineering, Materials Science, Polymer Science, or a related field from an accredited university and up to 3 years of relevant work experience; or a Master's in Bioengineering, Biomedical Engineering, Mechanical Engineering, Electrical Engineering, Materials Science, Polymer Science, or a related field from an accredited university and 5+ years of relevant subject matter work experience; or a Bachelor's in Bioengineering, Biomedical Engineering, Mechanical Engineering, Electrical Engineering, Materials Science, Polymer Science, or a related field from an accredited university and 10+ years of relevant subject matter specific work experience

Experience Requirements:

  • Willingness to become a testifying subject matter expert
  • Significant professional experience working within the medical device industry. 15+ years of experience in the industry preferred.
  • Experience and familiarity with Quality System Regulation 21 CFR Part 820 and ISO 13485.
  • Experience with risk management processes for medical devices, including experience with ISO 14971.
  • Experience and familiarity with FDA regulations. Experience with FDA audits/inspections preferred.
  • Experience and familiarity with laboratory procedures and testing, as well as the ability to execute and report on high-quality laboratory work.
  • Experience in forensic engineering of medical device failures. Knowledge of analytical techniques related to the failure of metals, alloys, composites, polymers, and glasses.
  • R&D and product development experience applicable to medical devices is highly desirable. Experience with product launch is preferred.
  • Hands-on experience in test method development, design of custom laboratory fixtures, data acquisition, and measurement system integration.
  • Demonstrated ability to decompose complex problems into actionable task lists by applying technical and critical thinking skills.

Skills Required:

  • Excellent written and oral communication skills.
  • A team player actively engaging others in accomplishing project work and office goals within their home office and across offices and other technical disciplines throughout ESI.
  • Demonstrated ability to work cross-functionally and effectively integrate with diverse subject matter experts.
  • Demonstrated project management skills.
  • Ability and desire to market ESi and grow the Biomedical Engineering specialty in the local and national markets.
  • Ability and desire to drive toward eventually becoming a Principal consultant within the firm.
  • Ability to interact with coworkers and clients professionally and desire to develop business internally and externally.
  • Demonstrated leadership ability and desire to mentor more junior staff.

Certifications:

  • Professional Engineer Licensure, RAC, PMP certifications are a plus.

Computer Skills Required:

  • Intermediate/advanced skills in Excel
  • Intermediate/advanced skills Word
  • Intermediate expertise in the use of engineering tools for testing, data analysis, and systems modeling (LabView, R, MATLAB, PYTHON, Abaqus, ANSYS, COMSOL, STAR-CCM+, Fluent, LMS Amesim, Analyze 14.0, FiJi/imageJ, etc.)
  • Knowledge of fundamental computational methods (Finite Element Analysis and Computational Fluid Dynamics).

Physical Demands:

The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is occasionally required to stand; walk and sit. Employee move be able to climb and crawl to perform investigations. Capable of working outside given range of ambient conditions. Ability to lift up to 50 pounds.

Work Environment:

The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. The noise level in the work environment is usually moderate.

To all recruitment agencies:ESi does not accept unsolicited resumes from search firms or agencies. Any resume submitted to any employee of ESi without a prior written search agreement will be considered unsolicited and the property of ESi. Please, no phone calls or emails.

It is the policy of ESI, as an equal opportunity employer, to attract and retain the best qualified individuals available, without regard to race/ethnicity, color, religion, national origin, gender, sexual orientation, age, disability, or veteran status. ESI is committed to recruiting, hiring, and promoting people with disabilities, as well as veterans. If you need assistance with completing the electronic application, please email your request to employment @ engsys.com

Applied = 0

(web-df9ddb7dc-vp9p8)