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<h3>Job Description</h3>
Job Description
About Blue Water Thinking
Guided by our principles of value generation, continuous innovation, customer-centricity, and vested collaboration, Blue Water Thinking proudly supports our Federal clients in achieving their Agency goals.
Founded by a decorated twenty-eight year Veteran of the United States Army, Blue Water Thinking understands and supports the mission of our Nation's war fighters, Veterans, their families and caretakers. 
Leveraging our executive team's military experience and private and public sector consulting expertise, Blue Water Thinking takes an integrated "one-team" approach and brings to bear best-fit solutions, thought leadership, and grit to meet our client's transformational needs.
Fueled by our values of integrity, respect, professionalism, stewardship and customer service, the Blue Water Thinking team understands the power of the human connection, collaboration, humility and loyalty to one another, our clients and industry partners.
Lastly, our formula for success is simple: Build something good, take care of our people, keep our clients satisfied, nurture our work ethic and reputation, build long-lasting partnerships, enjoy what we do and give back as much as possible.
Job Description
A Project Manager performs tasks requiring management of a small-scale project encompassing multiple tasks with a total life cycle budget and complexity comparable to the task order at hand. Tasks may include tracking and coordinating medical device and clinical system interfaces through the project lifecycle; formulating and defining system scope and objectives in accordance with the customer technical requirements; compiling and analyzing technical data; advising client management and customers on complex system projects and activities; working closely with customers to define communication systems and equipment requirements; providing instruction on and performing and documenting quality assurance reviews.
Qualifications
The Contractor personnel shall meet the following basic qualifications, regardless of role in the services provided under this contract:
<ul>
<li>Experience within a medical center and Biomedical Engineering department</li>
<li>Experience working in or with the Veterans Health Administration (VHA)</li>
<li>Understanding of VISN, VA medical center, and Biomedical Engineering department operations</li>
</ul>
Additional required qualifications:
<ul>
<li>A Bachelor's degree or higher in Engineering or Certification as a Clinical Engineer (CCE).</li>
<li>A minimum of three years of hospital or healthcare experience maintaining medical equipment or managing a hospital medical equipment program.</li>
<li>Must have proven experience working within the U.S. Department of Veteran's Affairs</li>
<li>Demonstrated knowledge of concepts related to computer based medical systems, networking protocols, and information security as it applies to medical technology within VHA.</li>
<li>Extensive experience designing, developing, and implementing clinical system interfaces with electronic health records, ensuring compliance with relevant standards and protocols (e.g., HL7, FHIR, DICOM).</li>
<li>Extensive experience in managing medical imaging systems, ensuring compliance with DICOM standards for image storage, retrieval, and transfer.</li>
<li>Proven ability to lead projects related to integrating biomedical devices and systems with Electronic Health Records (EHR) and Picture Archiving and Communication Systems (PACS) using HL7 and DICOM protocols.</li>
<li>Demonstrated skill in in communicating and working collaboratively with key stakeholders, including technical, clinical, and professional staff at various levels of the organization.</li>
<li>Understanding of regulatory agencies' requirements (TJC), industry regulatory requirements and International Standard Organization standards.</li>
</ul>
Eligibility:
<ul>
<li>Must be legally authorized to work in the United States without the need for employer sponsorship, now or at any time in the future</li>
<li>Must be able to obtain and maintain the required federal public trust clearance for this role</li>
</ul>
Compensation:
Salary for this position is determined by various factors, including but not limited to, location, the candidate's particular combination of knowledge, skills, competencies and experience, as well as contract specific affordability and organizational requirements. The proposed salary range for this position is outlined below.
Salary range: $90,000 - $115,000
Blue Water Thinking offers a comprehensive benefits package including health insurance (medical, dental and vision), paid time off, federal holidays, and matching 401K plan.
Our Commitment to Equal Employment Opportunity.
Blue Water Thinking, LLC (BWT) is committed to equal employment opportunity. We recruit, employ, train, compensate, and promote without regard to race, religion, color, national origin, age, sex, disability, protected veteran status, or any other basis protected by applicable federal, state, or local law.
Applying for this Job:
<ul>
<li>Resume must be submitted in word document format and must include dates in each section (experience, education, certifications...)</li>
<li>Candidates must fill out the below form to the best of their knowledge</li>
</ul>

Interfaces Project Manager - Biomedical Engineering

<h3>Job Description</h3>
Job Description
POSITION SUMMARY:
The Healthcare Imaging Engineer is responsible for the installation, maintenance, calibration, troubleshooting, and repair of medical imaging equipment, ensuring that all devices operate safely, reliably, and in compliance with manufacturer specifications and regulatory standards. This role works closely with radiology, cardiology, and other clinical departments to minimize downtime, enhance patient care, and optimize imaging system performance.
KEY RESPONSIBILITIES:
<ul>
<li> Install, configure, and test medical imaging systems (e.g., MRI, CT, X-ray, Ultrasound, PET, Nuclear Medicine, PACS).</li>
<li> Perform preventive and corrective maintenance in accordance with manufacturer guidelines, hospital policies, and applicable regulations (e.g., Joint Commission, FDA, state).</li>
<li> Troubleshoot and diagnose equipment malfunctions, coordinate with vendors and service providers when necessary.</li>
<li> Maintain accurate service records, work orders, and equipment histories in the CMMS.</li>
<li> Support imaging-related software, networks, and integration with hospital IT systems.</li>
<li> Ensure compliance with radiation safety protocols, electrical safety standards, and infection control policies.</li>
<li> Provide technical guidance and training clinical staff on proper use and care of imaging equipment.</li>
<li> Participate in capital equipment planning, procurement evaluations, and acceptance testing of new systems.</li>
<li> Stay current on emerging technologies, regulatory changes, and manufacturer updates.</li>
<li> Assist in on-call coverage and emergency response for imaging equipment failures.</li>
<li> Occasional after-hours or weekend work for urgent repairs and preventive maintenance.</li>
</ul>
REQUIRED KNOWLEDGE &amp; SKILLS:
<ul>
<li> Ability to read and interpret schematics, service manuals, and technical documentation.</li>
<li> Excellent problem-solving skills and ability to work under pressure.</li>
<li> Strong communication and customer service skills to interact effectively with clinical and technical staff.</li>
<li> Commitment to patient safety and confidentiality.</li>
</ul>
EDUCATION/EXPERIENCE/LICENSURE/TECHNICAL/OTHER:
<ul>
<li> Associate's or Bachelor's degree in Biomedical Engineering, Electrical Engineering, Electronics, or related field (or equivalent military or technical training).</li>
<li> Minimum 3-5 years' experience servicing complex imaging systems in a healthcare environment.</li>
<li> Strong knowledge of diagnostic imaging modalities and associated technologies.</li>
<li> Familiarity with DICOM standards, PACS/RIS integration, and networking principles.</li>
<li> Manufacturer certifications (e.g., GE, Siemens, Philips, Canon) preferred.</li>
</ul>
 
Must clear background and drug test required.

Healthcare Imaging Engineer, Biomedical Engineering, Full Time, Flex Shift, Job ID 1569550

Healthcare Imaging Engineer, Biomedical Engineering, Full Time, Flex Shift, Job ID 1569547

<h3>Job Description</h3>
Job Description
 
See yourself as a MoFe Engineer at Sightpath Medical!!
In addition to learning the latest innovations in the ophthalmic industry, Sightpath Medical offers a challenging and rewarding environment where you'll work with smart, fun and energetic people.
 &nbsp;• Sightpath Medical is the premier cataract and LASIK mobile services provider in the U.S. &nbsp;• We provide an independent working atmosphere &nbsp;• We provide on the job training to help you become an expert in our area of expertise &nbsp;• Salary position with quarterly bonus eligibility &nbsp;• 401(k) plan &nbsp;• Medical Benefits including medical, dental, vision, health savings account, short term disability, long term disability &nbsp;• Health and Wellness Program &nbsp; &nbsp;Responsibilities: &nbsp;• Requires the ability to install/de-install and operate transportable lasers and related equipment on one business unit at&nbsp;&nbsp;&nbsp; customer sites. &nbsp;• Responsible for calibration and programming of equipment for surgeon's approval prior to surgery being performed. &nbsp;• Responsible for the operation of both lasers when they are both required. &nbsp;• Provide routine preventative maintenance and repairs on the laser systems to maximize usage and minimize downtime. &nbsp;• Ability to troubleshoot, remove and replace components of the laser and calibrate to vendor specifications. &nbsp;• Responsible for maintaining all company assets in good working order. &nbsp;• Adherence to company standard operating procedures that meet/exceed standard of care. &nbsp;• Ability to complete Annual and Semi-Annual Preventative Maintenance checks and services on all assigned equipment. Successfully completes all PM paperwork during &nbsp;and at the end of PM. &nbsp;• Understands and adheres to proper sterile technique. &nbsp;• Other duties as required &nbsp; &nbsp;Qualifications: &nbsp;• Degree in Laser Electro-optics, Biomedical Electronics, Electronics or military training equivalent. &nbsp;• Proficiency with basic electronics and associated test equipment. &nbsp;• Able to work a varied work schedule and travel. &nbsp;• Able to work in a team environment. &nbsp;• Valid Driver's License &nbsp;• Ability to pass company administered road test. &nbsp;• Ability to occasionally lift 50 lbs. &nbsp;• Ability to stand for extended periods of time. &nbsp;• Able to work a varied work schedule and travel. &nbsp;• Great customer service skills.
 
 
PM25
 
Compensation details: 65000-70000 Yearly Salary
 
PI29ebf642656d-25405-38089402

MoFe Engineer I

<h3>Job Description</h3>
Job Description
 
We are seeking an Electrical engineer with embedded software &amp; electrical systems development experience to lead the design and integration of advanced digital visualization and illumination systems for next-generation flexible endoscopic devices. This is a highly technical, design-focused role centered on embedding miniature CMOS image sensors, fiber optic bundles, and LED illumination into millimeter-scale surgical instruments.
 
The Electrical Engineer will serve as the internal subject matter expert on imaging and illumination integration, working closely with electrical, mechanical, and firmware teams to ensure seamless performance and manufacturability of visualization subsystems. This person will play a key role in defining how the device captures and transmits images from inside the body, enabling life-saving endoscopic procedures.
This is an exciting opportunity to join a rapidly growing medical device startup and help pioneer novel visualization technologies that improve patient outcomes and empower physicians worldwide.
 
Day-to-Day
 
<ul>
<li>Lead the design, development, and integration of CMOS image sensors into flexible endoscopic platforms and subsystems.</li>
<li>Design, prototype, and optimize fiber optic and LED illumination assemblies for small-form-factor visualization systems.</li>
<li>Apply DFMA principles to optical and electronic subassemblies at the millimeter scale, ensuring manufacturability and reliability.</li>
<li>Develop and layout custom PCBs for imaging and illumination control using tools such as Altium, KiCAD, or Eagle.</li>
<li>Create precision CAD models and design mechanical fixturing, enclosures, and alignment hardware for optical/electronic components.</li>
<li>Collaborate cross-functionally with firmware, mechanical, clinical, regulatory, and manufacturing teams to achieve seamless integration and design control compliance.</li>
<li>Partner with OEMs and suppliers to source, validate, and qualify imaging and illumination components.</li>
<li>Support verification and characterization testing for imaging performance and system reliability.</li>
<li>Contribute to risk management (FMEA), design reviews, and design history documentation within an ISO 13485-compliant environment.</li>
<li>Serve as a technical mentor and thought leader within the visualization domain as the team scales.</li>
</ul>
 
Requirements / Qualifications
 
Required:
<ul>
<li>Bachelor’s or Master’s degree in Electrical, Optical, Biomedical, or Mechatronics Engineering (or related field).</li>
<li>7+ years of engineering experience, ideally in medical devices, imaging systems, or other highly regulated industries.</li>
<li>Proven hands-on experience integrating CMOS image sensors and fiber optic imaging systems.</li>
<li>Strong understanding of embedded electronics, firmware interfaces, and signal transmission.</li>
<li>Demonstrated experience with LED integration, optical coupling, and miniature illumination systems.</li>
<li>Proficiency with PCB design software (Altium, KiCAD, or Eagle).</li>
<li>Proficiency with CAD tools (SolidWorks preferred) for mechanical design and integration.</li>
<li>Deep experience applying design-for-manufacture/assembly (DFMA) principles to small-scale electro-optical assemblies.</li>
<li>Strong analytical, organizational, and communication skills, with the ability to thrive in a fast-paced startup environment.</li>
</ul>
 
Preferred:
<ul>
<li>Knowledge of ISO 13485, ISO 14971, and FDA QSR design control requirements.</li>
<li>Familiarity with IEC 60601 or other medical device safety standards.</li>
<li>Experience with image signal processing or embedded system design.</li>
<li>Background in fiber optics, medical imaging, or surgical visualization systems.</li>
<li>Prior experience in a startup or rapid product development environment.</li>
</ul>

Electrical Engineer

<h3>Job Description</h3>
Job Description
Are you an innovative Field Service Engineer with a passion for cutting-edge technology? Join Sightpath Medical, the premier provider of mobile cataract and LASIK services in the U.S. You’ll have the unique opportunity to work with advanced ophthalmic equipment while supporting top surgeons in a fast-paced and rewarding environment. Whether you’re an entry-level candidate or bring years of experience, we offer knowledge, collaboration, and a shared commitment to excellence.
 
Why Sightpath Medical?
<ul>
<li>Comprehensive Training: Gain hands-on experience with the latest in ophthalmic laser technology. We provide all the training you need to excel in the field.</li>
<li>Independent Work Environment: You’ll have the autonomy to manage your work effectively while being part of an expert team.</li>
<li>Travel: You will have ownership of an assigned territory you will manage with a company provided vehicle and equipment. Every day is different. You will move from facility to facility providing expert service to our customers.</li>
<li>Work-life balance: With 8-10 case days per month, enjoy flexibility on non-case days when working from home or while traveling.</li>
<li>Medical benefits including health, dental, vision, short/long-term disability, and health savings account.</li>
<li>401(k) plan with employer contribution.</li>
<li>Health and Wellness Program to support your well-being.</li>
</ul>
 
What You’ll Do:
<ul>
<li>Technical Expertise: Install, de-install, calibrate, and operate transportable lasers and related equipment at customer sites.</li>
<li>Surgical Support: Ensure all equipment is programmed and calibrated to surgeon specifications prior to surgeries. You will also support the Surgeons during surgery to ensure customer satisfaction.</li>
<li>Preventative Maintenance: Perform routine maintenance and repairs to maximize equipment performance and minimize downtime.</li>
<li>Troubleshooting: Diagnose and resolve equipment issues efficiently, ensuring seamless surgical procedures.</li>
<li>Sterile Technique and Clinical: Adhere to sterile techniques during surgeries to ensure patient safety. Comprehensive training will be provided for all clinical aspects and requirements.</li>
<li>Manual Labor: Willing and able to assist with equipment setup and transport.</li>
<li>Other Duties: Flexibility to take on additional responsibilities as required.</li>
</ul>
 
Who We’re Looking For:
<ul>
<li>Technical Degree: Degree in Laser Electro-optics, Biomedical Equipment Technology, Electronics, or a similar field; military training in related fields is also acceptable.</li>
<li>Hands-On Experience: Proficiency with basic electronics and test equipment. Experience with laser systems is a plus.</li>
<li>Adaptable and Travel-Ready: Comfortable with driving to various locations in assigned territory and staying overnight when needed. All travel expenses are covered (hotel stays, gas for company vehicle, and meal allowances while traveling).</li>
<li>Driving Record: Able to produce a valid driver's license and pass a Motor Vehicle Report (MVR)/ driving record.</li>
<li>Excellent Communicator: Able to build strong relationships quickly with surgeons and their teams.</li>
<li>Self-assured: Able to thrive in high-pressure environments with confidence and professionalism.</li>
<li>Organized and Detail-Oriented: Skilled at managing equipment and completing administrative tasks required to support assigned territory.</li>
<li>Physical Demands: Ability to lift up to 100 lbs. and stand for extended periods.</li>
</ul>
 
Relocation Assistance:
We offer relocation allowances for qualified candidates who may need to move to join our team.&nbsp;
 
Compensation Range:
<ul>
<li>$65,000 - $80,000 annually with bonus eligibility</li>
<li>Company credit card provided for company use including: hotel stays, gas for company vehicle, maintenance for vehicle, meal allowance (when an overnight stay is required for coverage purposes), etc.</li>
</ul>
SIGHTPATH is an equal opportunity employer. In accordance with applicable law, we prohibit discrimination based on race, color, religion, creed, gender, pregnancy or related medical conditions, age (40 and over), national origin or ancestry, physical or mental disability, genetic information or any other consideration protected by federal, state or local laws. Our commitment to equal opportunity employment applies to all persons involved in our operations and prohibits unlawful discrimination by any employee, including supervisors and coworkers.
 
PM25
 
Compensation details: 60000-75000 Yearly Salary
 
PI2e18efc81bb8-25405-38196172

Laser Engineer III

<h3>Job Description</h3>
Location:&nbsp;Woburn, MA
 
Vaxess is an NIH and venture-funded company developing a pipeline of next-generation therapeutics on the Microneedle Array Patch (MAP) platform. With only five minutes of wear-time on the skin, the self-applied MAP enables sustained delivery in the skin. The platform combines high temperature stability with simplified application to dramatically alter the way that drugs are delivered. Vaxess is committed to enabling products that are not only more effective, but also more accessible to patients around the world. 
 
Manufacturing at Vaxess is cross-disciplinary, integrating mechanical, industrial, biomedical, and chemical engineering with chemistry, biology, and human factors to address important unmet medical needs. We are seeking a talented, collaborative, and highly motivated Formulation engineer with a proven track record in leading Process Development, Tech Transfer as well as manufacturing support. The Formulation Engineer will report to the Director of Process Development and will collaborate closely with cross-functional teams such as Manufacturing, Assay Development, Quality Control, Automation, and Facilities.&nbsp;
 
Responsibilities
<ul>
<li>Leads and supervises cGMP formulation operations related to Microarray Patch manufacturing, ensuring adherence to batch records, SOPs, and regulatory requirements. Provides hands-on guidance and oversight to junior staff and technicians during manufacturing campaigns.</li>
<li>Oversees day-to-day manufacturing floor activities during formulation operations, ensuring safety, compliance, and productivity. Coordinates scheduling, resource allocation, and troubleshooting in collaboration with Manufacturing and Facilities teams.</li>
<li>Trains, mentors, and evaluates manufacturing personnel involved in formulation processes. Develops and implements training materials and competency assessments to ensure operational excellence and compliance.</li>
<li>Reviews and verifies documentation for completeness and compliance with regulatory standards. Ensures the timely completion of production batch records, logbooks, test records, and other documentation following Good Documentation Practices.</li>
<li>Collaborates on process development and optimization studies for Microarray Patch formulations. Works as part of the process development team to optimize excipients and formulations to support project objectives. Maintains detailed experimental records. Documents data in reports and write detailed protocols.</li>
<li>Collaborates closely with cross-functional team members of Manufacturing, Quality, Research, and Automation functions to support process development, manufacturing, and tech transfer between R&amp;D and product development activities. Acts as a liaison between Research and Manufacturing teams to scale up formulation processes from R&amp;D to production.&nbsp;</li>
<li>Identifies and implements new technologies and assays to support continuous improvement and scale up of processes.</li>
<li>Leads root cause analyses (RCA) and process development investigations.</li>
<li>Authors, edits, and reviews batch records, SOPs, work instructions, and other documentation to support manufacturing readiness and regulatory submissions.</li>
<li>Regularly communicates progress, issues, and results to key stakeholders.</li>
</ul>
 
Qualifications
<ul>
<li>BS or MS in Biological Sciences, Chemistry, Biomedical Engineering, Chemical Engineering or a related discipline, with at least 3 years of relevant experience. Title will be adjusted commensurate with qualifications.</li>
<li>Strong prior hands-on formulation process development experience. Demonstrated ability to design, execute studies, and analyze experimental results.</li>
<li>Prior supervisory experience in a GxP environment is preferred.</li>
<li>Strong understanding of Good documentation practices. Experience in authoring and reviewing batch records, SOPs, and work instructions.</li>
<li>Strong verbal and written communication skills. Excellent time and project management skills. </li>
<li>Demonstrated ability to learn new skills, creatively solve challenging technical problems, think independently, and work collaboratively in diverse multidisciplinary teams.</li>
<li>Strong attention to detail. Ability to identify root causes of problems and recommend corrective actions for continuous process improvement.</li>
</ul>

Formulation Engineer

<h3>Job Description</h3>
Position Title: Quality Engineer
Location: Boston, Massachusetts
Duration: Long-Term Project
 
Key Responsibilities:
<ul>
<li>Design Assurance &amp; Risk Management:</li>
<li>Lead design assurance activities for new and existing medical devices, including risk management per ISO 14971. Participate in design reviews to ensure product safety, reliability, and compliance with internal and regulatory standards.</li>
<li>Test Method Development &amp; Validation:</li>
<li>Develop, validate, and implement test methods, inspection procedures, and sampling plans to verify product and process performance. Ensure accuracy and repeatability in test methodologies.</li>
<li>Product Launch &amp; Design Transfer:</li>
<li>Support new product introduction (NPI) activities, ensuring smooth design transfer from R&amp;D to manufacturing. Partner with operations and process engineering to validate manufacturing processes and establish robust control plans.</li>
<li>Change Control &amp; Quality Documentation:</li>
<li>Manage change control processes for product and process modifications. Draft, review, and maintain SOPs, work instructions, and technical documentation to ensure compliance with company and regulatory requirements.</li>
<li>Supplier Quality &amp; Audits:</li>
<li>Collaborate closely with suppliers to maintain component and material quality. Participate in supplier qualification, monitoring, and audit activities. Support internal and external audits, CAPA, and continuous improvement initiatives.</li>
<li>Continuous Improvement:</li>
<li>Identify opportunities to enhance product quality and manufacturing efficiency. Apply root cause analysis, risk-based thinking, and lean principles to drive corrective and preventive actions.</li>
</ul>
Qualifications &amp; Requirements:
<ul>
<li>Bachelor’s or master’s degree in engineering, biomedical engineering, mechanical engineering, or a related technical discipline.</li>
<li>3–7 years of experience in medical device quality engineering, design assurance, or product development support.</li>
<li>Hands-on experience with catheters, guidewires, or other Class II/III medical devices is highly desirable.</li>
<li>Strong working knowledge of ISO 13485, 21 CFR Part 820 (QSR), ISO 14971, and other applicable global medical device regulations.</li>
<li>Proven ability to interpret engineering drawings, specifications, and test data.</li>
<li>Excellent analytical, documentation, and problem-solving skills with strong attention to detail.</li>
<li>Effective communication and collaboration skills with cross-functional and supplier teams.</li>
</ul>

Quality Engineer

<h3>Job Description</h3>
Our client, a Global Leader in the Medical Device Industry has an immediate opening for a Sr. Systems Engineer for a 14 month + Contract. Our client offers results-driven people a place where they can make a difference - every day! You will also have the opportunity to work with other like-minded, self-directed and detail oriented Top Talents in an extremely collaborative and professional environment.
Work with the engineering team to solidify a new implant and instrument design control and risk management structure, based on a systems engineering approach. Develop architecture documents and use cases to help establish tiering of requirements as well as trace matrixes for design verification and validation.

Help with scoping of the JR implant and instrument portfolio and translation from legacy design controls to this new structure.

Implement this structure to work within the Jama requirements software system. 
Position Description (Principle Duties and Responsibilities)
Technical Responsibilities: 
<ul>
<li>Research, design, develop, modify, and verify medical device systems.</li>
<li>Translate user needs to system requirements.</li>
<li>Modify existing system architectures or test designs.</li>
<li>Create new system architectures or test designs for simple product or features.</li>
<li>Contribute to design decomposition using, modeling, simulation, budgeting, or mathematical techniques.</li>
<li>Apply fundamental and some advanced concepts, practices and procedures for problem solving. </li>
<li>Contribute to Product Risk Management activities.</li>
<li>Develop system architecture for joint replacement instrumentation design controls and risk management.</li>
<li>Translate legacy requirements to new requirements in order to facilitate a systems approach and consolidated design controls and risk management.</li>
</ul>

Business Responsibilities:
<ul>
<li>Demonstrate advanced understanding of customer needs and design inputs.</li>
<li>Demonstrate proficiency with product's intended use and clinical procedures.</li>
<li>Learn how the financial models are constructed. </li>
</ul>
 
Med Device Compliance:
<ul>
<li>Follow fundamental industry standards, design requirements and test strategies which apply to regulatory requirements. </li>
<li>Independently create or refine engineering documentation, such as the Design History file.</li>
<li>Follow R&amp;D procedure like design controls and risk management, per the Quality Management System. </li>
</ul>
 
General Responsibilities: 
<ul>
<li>Under minimal supervision, work with all stakeholders to ensure project success. </li>
<li>Quickly process and assimilate procedures, policies, processes, systems, and technology required.</li>
<li>Work on complex problems, applying advanced experience and learnings.</li>
<li>Demonstrate ownership and prioritize work with minimal supervision.</li>
<li>Works as key member of the team, collaborating with others and solidifying relationships.</li>
</ul>
 
Qualifications
<ul>
<li>Bachelor of Science in Software, Electrical, Mechanical, Systems, or Biomedical Engineering &amp; 2+ years of work experience.</li>
</ul>
Technical Skills: 
<ul>
<li>Working knowledge and understanding of requirement and verification practices.</li>
<li>Working knowledge of Requirements Management Tools.</li>
<li>Ability to communicate basic plans and technical information to team members.</li>
</ul>
 
Preferred Skills / Engineering tools: 
<ul>
<li>Requirements Management Software, especially Jama.</li>
<li>Experience with SysML and Model-based Systems Engineering.</li>
<li>Experience with SysML / MBSE software tools.</li>
<li>Knowledge of ISO 13485 and ISO 14971.</li>
</ul>
 
Certifications:
INCOSE ASEP certified, or equivalent

Sr Systems Engineer

<h3>Job Description</h3>
Job DescriptionSalary: $115,000 - $130,000/year 
ATI has a current need for an Electrical Engineer to provide electrical system design, project management, and construction administration to support renovation of biomedical research laboratories at the National Institutes of Health (NIH) in Bethesda, Maryland.
 
Great Pay and Benefits for an Electrical Engineer
 
<ul>
<li>$115,000 - $130,000 annual salary depending on qualifications and experience;</li>
<li>11 annual paid holidays;</li>
<li>Paid annual vacation and sick leave;</li>
<li>Employee and family health, dental, prescription, and vision insurance with 75% of the premiums paid by the company;</li>
<li>401(k) plan with 4% employer match vesting immediately;</li>
<li>Employer paid short-term and long-term disability, and life insurance;</li>
<li>Professional development assistance including memberships, professional licenses, and tuition reimbursements; and</li>
<li>Opportunity to work remotely for two days/week.</li>
</ul>
 
Candidate Requirements for an Electrical Engineer
<ul>
<li>Bachelors degree in a related discipline OR 10+ years of experience with electrical systems and their design;</li>
</ul>
<ul>
<li>Minimum 3+ years of experience in an architecture, engineering, and/or construction environment;</li>
</ul>
<ul>
<li>Understanding of applicable electrical building design standards and codes such as the National Fire Protection Association (NFPA), National Electrical Code (NEC), and International Building Code (IBC) is required;</li>
<li>Specific skills required include circuit lighting and power, fill in panel schedules, motor circuit sizing, lighting calculations, SKM Power Tools, and fire alarm system design and devices layout;</li>
<li>Proficiency in electrical design using AutoCAD and REVIT;</li>
<li>Background in healthcare and/or laboratory electrical design is a plus; and</li>
<li>Ability to secure an NIH clearance in a timely manner is also required.</li>
</ul>
About ATI
 
ATI, Inc.(<a href="http://www.atiinc.com" target="_blank">www.atiinc.com</a>) is a full-service consulting firm with over 45 years of experience solving complex facility and program management, construction, and environmental challenges for government and private sector clients. Committed to industry leadership, we deliver sustainable, innovative, and cost-effective solutions that drive results and prioritize client satisfaction. At the same time, we foster a dynamic, growth-oriented workplace where employees can thrive.
Qualified candidates are encouraged to submit a resume as soon as possible. This job description is not intended to be all-inclusive. Selected candidate may perform other related duties as assigned to meet the ongoing needs of the organization.

 
ATI, Inc. provides equal employment opportunities to all qualified individuals, including protected groups, protected veterans and individuals with disabilities. ATI complies with applicable local, state and federal laws governing nondiscrimination in employment at each location the Company operates. This policy applies to all terms and conditions of employment, including, but not limited to hiring, placement, promotion, termination, leaves of absence, compensation, and training. ATI is an E-Verify Employer in the United States. ATI will provide reasonable accommodations with the application process upon your request as required to comply with applicable laws. If you have a disability and require assistance in this application process, please let your recruiter know.

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