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<h3>Job Description</h3>
General Summary
John Moriarty &amp; Associates of Virginia (JMAV) is seeking a Summer 2026 Intern in the Charlottesville, VA area.
 
Interns with Moriarty are responsible for assisting the project team with direction to ensure that the project is built according to plan, specification, schedule, and quality.
 
The intern should be located within daily driving distance of the Charlottesville, VA area.
 
Roles &amp; Responsibilities:
The intern must have the basic ability to read and interpret plans &amp; drawings, understand the importance of jobsite safety, and be able to effectively present information. Some responsibilities include:
<ul>
<li>Assist field personnel in their site-specific responsibilities.</li>
<li>Assist field personnel in quality control inspections and documentation.</li>
<li>Ability to perform construction material takeoffs and make estimates for future needs.</li>
<li>Understand company / project safety plan.</li>
<li>Assist with administration of subcontractor safety training and compliance.</li>
<li>Asist with coordinating subcontractor deliverables for project execution.</li>
<li>Assist in processing submittals.</li>
</ul>
Education:
<ul>
<li>Working towards a 4-year degree preferred, in Building Construction or relevant subject.</li>
</ul>
 
Work Experience: 
<ul>
<li>0-2 years of project management experience, in Construction is preferred.</li>
</ul>
 
Knowledge, Skills, and Abilities:
<ul>
<li>Excellent communication skills, both verbal and written</li>
<li>Adaptable team players, with strong client service skills</li>
<li>Basic understanding of construction drawings and specifications</li>
<li>Basic understanding area schedules</li>
<li>Basic knowledge of Microsoft Excel and Smartsheet scheduling</li>
</ul>
 
Physical Requirements:
<ul>
<li>This position will require moderate physical activity</li>
<li>Driving between sites, climbing stairs and ladders, walking on rough terrain, standing for extended periods of time</li>
</ul>
 
Work Environment:
<ul>
<li>Work onsite, outdoors, in all weather conditions. The noise in these work environments is usually moderate to very loud. The employee will be regularly exposed to outside weather conditions.</li>
</ul>
 
The Company:
John Moriarty &amp; Associates of Virginia (JMAV) is a privately held general contractor that specializes in large scale, urban, ground-up projects such as mixed-use, multi-family, hotels, senior living, student housing and bio-medical and is one of the faster growing contactors in the DC-Metro area. Exceptional for the industry, 100% of our projects are negotiated with over 85% being with repeat clients.
 
Our approach is characterized by transparency, collaboration, attention to detail and hands-on leadership. Our projects are set up for success by our strong emphasis on pre-construction services and planning, proper staffing and hiring best-in-class subcontractors. Our growth has been a result of outstanding execution in every phase of project delivery and an unparalleled employee retention of the best people in the industry.
 
Our parent company, John Moriarty &amp; Associates (JMA), was founded in 1985 in Winchester, MA and is one of the most respected general contracting firms in the industry. Learn more about us at <a href="http://www.jma-va.com" target="_blank">www.jma-va.com</a> and <a href="http://www.jm-a.com" target="_blank">www.jm-a.com</a>.
 
John Moriarty &amp; Associates of Virginia participates in E-Verify for all hired employees. E-Verify is a web-based system that allows enrolled employers to confirm the eligibility of their employees to work in the United States by electronically matching information provided by employees on the Form I-9 against records available to the Social Security Administration and the Department of Homeland Security. More information can be found at <a href="http://www.e-verify.gov" target="_blank">www.e-verify.gov</a>.

Field/Office Engineer Intern (Summer 2026)

<h3>Job Description</h3>
General Summary
John Moriarty &amp; Associates of Virginia (JMAV) is seeking a Summer 2026 Intern in the Washington DC Metro area.
 
Interns with Moriarty are responsible for assisting the project team with direction to ensure that the project is built according to plan, specification, schedule, and quality.
 
The intern should be located within daily driving distance of the Washington DC Metro area.
 
Roles &amp; Responsibilities:
The intern must have the basic ability to read and interpret plans &amp; drawings, understand the importance of jobsite safety, and be able to effectively present information. Some responsibilities include:
<ul>
<li>Assist field personnel in their site-specific responsibilities.</li>
<li>Assist field personnel in quality control inspections and documentation.</li>
<li>Ability to perform construction material takeoffs and make estimates for future needs.</li>
<li>Understand company / project safety plan.</li>
<li>Assist with administration of subcontractor safety training and compliance.</li>
<li>Asist with coordinating subcontractor deliverables for project execution.</li>
<li>Assist in processing submittals.</li>
</ul>
Education:
<ul>
<li>Working towards a 4-year degree preferred, in Building Construction or relevant subject.</li>
</ul>
 
Work Experience: 
<ul>
<li>0-2 years of project management experience, in Construction is preferred.</li>
</ul>
 
Knowledge, Skills, and Abilities:
<ul>
<li>Excellent communication skills, both verbal and written</li>
<li>Adaptable team players, with strong client service skills</li>
<li>Basic understanding of construction drawings and specifications</li>
<li>Basic understanding area schedules</li>
<li>Basic knowledge of Microsoft Excel and Smartsheet scheduling</li>
</ul>
 
Physical Requirements:
<ul>
<li>This position will require moderate physical activity</li>
<li>Driving between sites, climbing stairs and ladders, walking on rough terrain, standing for extended periods of time</li>
</ul>
 
Work Environment:
<ul>
<li>Work onsite, outdoors, in all weather conditions. The noise in these work environments is usually moderate to very loud. The employee will be regularly exposed to outside weather conditions.</li>
</ul>
 
The Company:
John Moriarty &amp; Associates of Virginia (JMAV) is a privately held general contractor that specializes in large scale, urban, ground-up projects such as mixed-use, multi-family, hotels, senior living, student housing and bio-medical and is one of the faster growing contactors in the DC-Metro area. Exceptional for the industry, 100% of our projects are negotiated with over 85% being with repeat clients.
 
Our approach is characterized by transparency, collaboration, attention to detail and hands-on leadership. Our projects are set up for success by our strong emphasis on pre-construction services and planning, proper staffing and hiring best-in-class subcontractors. Our growth has been a result of outstanding execution in every phase of project delivery and an unparalleled employee retention of the best people in the industry.
 
Our parent company, John Moriarty &amp; Associates (JMA), was founded in 1985 in Winchester, MA and is one of the most respected general contracting firms in the industry. Learn more about us at <a href="http://www.jma-va.com" target="_blank">www.jma-va.com</a> and <a href="http://www.jm-a.com" target="_blank">www.jm-a.com</a>.
 
John Moriarty &amp; Associates of Virginia participates in E-Verify for all hired employees. E-Verify is a web-based system that allows enrolled employers to confirm the eligibility of their employees to work in the United States by electronically matching information provided by employees on the Form I-9 against records available to the Social Security Administration and the Department of Homeland Security. More information can be found at <a href="http://www.e-verify.gov" target="_blank">www.e-verify.gov</a>.

<h3>Job Description</h3>
Job Description
PURPOSE OF THE POSITION:
To conceptualize, prototype, design, and bring new medical devices from inception through manufacturing and launch following a formal and regulated medical device design control process
RESPONSIBILITIES:
<ul>
<li>Specific product/process design and project management duties include but are not limited to the development, formulation, documentation, and project management activities associated with: concept and prototype development, formulation of design requirements, Design and Process Failure Modes and Effects Analysis, Risk Analysis, design/process verification and validation test methods (protocols, statistical analysis and reports), manufacturing transfer, design history file, design reviews, post launch continuous improvement and design change.</li>
<li>Create new product designs and specifications integrating Marketing, Sales, Manufacturing and Regulatory requirements to meet user needs (i.e. surgeon, clinical staff, patient)</li>
<li>Create 3D models and 2D engineering specification drawings utilizing 2D-3D CAD (i.e. SolidWorks)</li>
<li>Manage project plan (e.g. Gantt chart), maintain project team meeting minutes and/or senior management updates from initial concept through product launch</li>
<li>Provide support and collaborate with cross functional groups and management in and outside the core design team (i.e. Regulatory, Quality, Manufacturing, and Sales &amp; Marketing) throughout the product development cycle.</li>
<li>Exercise creativity in concept design through product development and manufacturing</li>
<li>Be able to incorporate design for manufacturing (DFM) into prototype and product design</li>
<li>Exercise organization and presentation skills in effectively leading and managing multiple projects (e.g. new product development, sustaining engineering, continuous improvement, etc.)</li>
<li>Understand and clearly articulate the clinical application of devices being developed</li>
<li>Understand and utilize the company’s product development process and associated procedures</li>
<li>Train and adhere to applicable procedures per the company’s Quality Management System</li>
<li>Knowledge of plastic injection mold design and process</li>
</ul>
GENERAL OBJECTIVES:
<ul>
<li>Complete projects on schedule and within budget</li>
<li>Gain and utilize product and clinical application knowledge of devices used in the endoscopic market</li>
<li>Understand and apply design control procedures used by ETI</li>
<li>Design devices that will readily transition to ETI Manufacturing</li>
</ul>
QUALITY OBJECTIVES:
<ul>
<li>Conduct product development and design control in compliance with all applicable standards and guidelines (i.e. FDA 21 CFR, ISO 9001, ISO 13485, ISO 60601, cGMP, etc.)</li>
<li>Create test protocols that will accurately verify and validate design inputs</li>
<li>Stay current and trained on applicable procedures, standards and guidelines</li>
</ul>
EXPERIENCE REQUIRED:
<ul>
<li>Bachelor's degree in either Mechanical, Manufacturing, Biomedical Engineering or a relevant and applicable field of study with at least two years of post-degree work preferably in a medical device environment.</li>
<li>Preferably 3 years of Medical Device Design experience in gastroenterology, urology, cardio-cath./stent, arthroscopy, or other relevant least/minimally invasive endoscopic medical device design</li>
<li>Experience in applying design control and cGMP’s for Class I and II, IIa, IIb medical devices</li>
<li>Experience applying analytical tools including: GD&amp;T, dFMEA, pFMEA, Risk Analysis, Statistical Analysis</li>
<li>Project management skills</li>
<li>Solid Works or other 3D modeling software</li>
<li>Knowledge of plastic injection mold design and processes preferred</li>
<li>Excellent technical writing, communication and presentation skills</li>
</ul>
TRAINING PREFERRED:
Training including:
<ul>
<li>Lean Six Sigma Green or Black Belt Training (including applied statistical methods)</li>
<li>Gastroenterology or general endoscopic surgical technique seminars</li>
<li>Engineering professional development courses on project management</li>
<li>Training for Regulatory awareness of ISO 13485 and FDA GMP’s</li>
</ul>
COMMENTS:
Must maintain the reputation of ETI for outstanding customer relationship/support throughout the development process
Company DescriptionEndo-Therapeutics, Inc. is a medical device manufacturing company that takes great pride in our innovative products, exceptional quality, and, most importantly, our unique company culture. At Endo-Therapeutics, we firmly believe that a diverse and inclusive environment fosters creativity, collaboration, and excellence, enabling us to deliver cutting-edge solutions to meet the evolving needs of the healthcare industry. Our commitment to creating a great culture of inclusiveness sets us apart. We believe that diverse perspectives and backgrounds fuel innovation and drive our success. We celebrate individuality and actively promote an environment where every employee feels valued, respected, and empowered to contribute their unique talents and ideas. In addition to our commitment to inclusivity, we pride ourselves on our relentless pursuit of excellence in everything we do. We have assembled a highly skilled and passionate team of professionals who are driven by a shared dedication to improving patient outcomes. Through continuous innovation and rigorous quality standards, we ensure that our medical devices meet the highest industry standards and deliver exceptional performance in the hands of healthcare professionals. As an organization, we embrace a collaborative approach that encourages open communication and teamwork. We foster an environment where ideas are shared, challenges are overcome together, and everyone is empowered to contribute their expertise. This collective effort allows us to develop comprehensive solutions that address the complex and evolving needs of healthcare providers and patients alike. We invite you to partner with Endo-Therapeutics, Inc. and experience firsthand our commitment to inclusiveness, innovation, and excellence. Together, we can drive advancements in medical device manufacturing, improve patient care, and make a positive impact on the healthcare industry. 
<h3>Company Description</h3>
Endo-Therapeutics, Inc. is a medical device manufacturing company that takes great pride in our innovative products, exceptional quality, and, most importantly, our unique company culture. At Endo-Therapeutics, we firmly believe that a diverse and inclusive environment fosters creativity, collaboration, and excellence, enabling us to deliver cutting-edge solutions to meet the evolving needs of the healthcare industry.\r\n\r\nOur commitment to creating a great culture of inclusiveness sets us apart. We believe that diverse perspectives and backgrounds fuel innovation and drive our success. We celebrate individuality and actively promote an environment where every employee feels valued, respected, and empowered to contribute their unique talents and ideas.\r\n\r\nIn addition to our commitment to inclusivity, we pride ourselves on our relentless pursuit of excellence in everything we do. We have assembled a highly skilled and passionate team of professionals who are driven by a shared dedication to improving patient outcomes. Through continuous innovation and rigorous quality standards, we ensure that our medical devices meet the highest industry standards and deliver exceptional performance in the hands of healthcare professionals.\r\n\r\nAs an organization, we embrace a collaborative approach that encourages open communication and teamwork. We foster an environment where ideas are shared, challenges are overcome together, and everyone is empowered to contribute their expertise. This collective effort allows us to develop comprehensive solutions that address the complex and evolving needs of healthcare providers and patients alike.\r\n\r\nWe invite you to partner with Endo-Therapeutics, Inc. and experience firsthand our commitment to inclusiveness, innovation, and excellence. Together, we can drive advancements in medical device manufacturing, improve patient care, and make a positive impact on the healthcare industry.

Product Development Engineer II

<h3>Job Description</h3>
Job DescriptionCompany Description 
Sirtex Medical is a global leader in healthcare, with offices in the U.S., Australia, Germany, and Singapore, dedicated to&nbsp;improving patient outcomes.&nbsp;
Our mission is to be at the forefront of minimally invasive cancer and embolization therapies. By partnering with&nbsp;physicians, we aim to provide innovative products that enhance patient outcomes and simplify treatments. Achieving&nbsp;this ambitious goal requires passionate and talented individuals who are committed to making a difference. Our flagship&nbsp;product, SIR-Spheres® Y-90 resin microspheres, is a targeted radiation therapy for liver cancer. To date, we have&nbsp;delivered over &gt;150K doses across 50+ countries, significantly impacting patients' lives worldwide. Our success is fueled&nbsp;by our dedication to serving the medical community, maintaining professionalism, fostering a collaborative work culture,&nbsp;nurturing an entrepreneurial spirit, and continuously pursuing innovation and improvement.&nbsp;
At Sirtex, we are committed to creating a great workplace. We offer a range of benefits, programs, and services to&nbsp;support our employees, ensuring they have opportunities to contribute to our success and advance their careers. Join&nbsp;our inclusive community, where you can collaborate with talented colleagues, bring your ideas to life, and advance your&nbsp;career, all while delivering innovative healthcare solutions to patients.
Job Description 
A Product Development Engineer (Level Senior) is responsible in developing new technologies, products, materials, processes, or equipment with minimal supervision. Independently, or as a member of a team leading technically and cross functionally, develops, directs, and executes plans for a major segment of complex projects. Compiles and analyzes operational, test, and research data to establish technical specifications for designing or modifying products, processes, and materials.
NOTE: This position is an onsite position with a hybrid arrangement (currently 3 days/week in office and 2 days/week remote.&nbsp; Candidates must be able to report to the office weekly.
<ul>
<li>Successfully completes complex engineering work in one or more of the following: technology development, product design and development, test of materials or products, preparation of specifications, process study, research investigation (animal and clinical studies), and report preparation.</li>
<li>Select techniques to solve complex problems and make sound design recommendations.</li>
<li>Designs and prepare complex reports to communicate results to technical community.</li>
<li>Designs and coordinates complex engineering tests and experiments.</li>
<li>Assesses the feasibility and soundness of proposed engineering evaluation tests, products or equipment.</li>
<li>Interfaces with Physicians/Lab personnel to obtain feedback on concepts and performance of new devices.</li>
<li>Works cooperatively with operation, quality, manufacturing, regulatory, clinical, and marketing on complex projects to ensure project success.</li>
<li>May train and/or provide work directions to interns, technicians and entry-level engineers.</li>
<li>Fully participates in and successfully contributes to project teams including the following activities: product design and development, test of materials, preparation of specifications, process capability studies, research investigations (animal and clinical studies), report preparation, and process/test documentation.</li>
<li>Perform product verification and validation testing, to ensure high-quality results and compliance with industry standards.</li>
<li>Develop and maintain detailed product technical specifications, engineering drawings, and bill of materials (BOM).</li>
<li>Designs, procures, and fabricates tooling and fixtures.</li>
<li>Performs troubleshooting on new products/process problems related to design, material, or process.</li>
<li>Collaborate with suppliers and vendors to source materials and components for product development.</li>
<li>Evaluate and incorporate feedback from customers, end-users, key opinion leaders (KOL) and other stakeholders to improve product designs.</li>
<li>Lead inter-disciplinary technical reviews intended to provide a systematic assessment of design results, device design and Design for Manufacturability (DFM). Create, draft and release technical reports required for product/process development programs.&nbsp;</li>
<li>Lead the design knowledge transfer of new manufacturing processes and provide training to product builders and technicians.</li>
<li>Establish and maintain appropriate design controls documentation, design trace matrices, design history files, technical files and device master records.&nbsp;</li>
<li>Develop and execute required validations per QMS requirements to include Equipment, Process &amp; Product validations.</li>
</ul>
Qualifications 
<ul>
<li>Bachelor’s of Science degree in Mechanical Engineering, Biomedical Engineering, Chemical Engineering, Plastics Engineering or a related field. Master of Science&nbsp;degree is preferred.</li>
<li>5+ years of in-depth conceptual, practical and technical and/or functional knowledge of principles of product development required.</li>
<li>Medical Device experience is required</li>
<li>Solves a significant range of problems of varying scope and complexity.&nbsp;Exchange&nbsp;complex information with others, potentially guiding and influence others.</li>
<li>May lead complex&nbsp;projects with high level of risks and resource requirements</li>
<li>Applies understanding of key business drivers in the context of the organization's industry and how closely related teams integrate with others to accomplish their objectives and drive efficiencies.</li>
<li>Supports team members by setting an example, coaching and providing feedback and guidance.</li>
<li>Works independently guided by company policies, guidelines and procedures, receiving guidance on complex and unprecedented problems.</li>
<li>Impacts quality and effectiveness of customer, operational, project/program or service activities within own team and other related teams.</li>
<li>Regularly participates in discussions and presentations in cross-functional meetings, logically presenting information to convey key messages with SLT and middle management teams.&nbsp;</li>
</ul>
The target base salary range for this position will range from $104,000 to $126,000 annually.&nbsp;Individual compensation for this job requisition will be based on non-discriminatory factors, including your geographic location, skills, experience, education and other factors as they relate to the position requirements.&nbsp; Actual compensation may vary depending on the confirmed job-related skills and experience.
In addition to the expected base compensation, this role is eligible to participate in Sirtex’s incentive programs (target bonus of 5%&nbsp;for this position)&nbsp;and benefit plans, which include paid sick and vacation time, health insurance and a generous 401k matching program.
 Additional Information 
All your information will be kept confidential according to EEO guidelines.
Do you want to be part of something bigger? A team whose impact stretches across the globe making a real difference to the quality of people’s lives.&nbsp; Sirtex recognizes that well-being, financial health, and work-life balance are crucial for our employees to achieve personal success.&nbsp;
Sirtex offers qualified candidates:
<ul>
<li>Diverse and flexible work arrangements to achieve the optimum balance between work and personal responsibilities.</li>
<li>A culture of respect, diversity, collaboration, and innovation fostering inclusiveness and superior performance.</li>
<li>Attractive compensation and benefit packages which are practical, robust and equitable.</li>
<li>A commitment to support ongoing professional growth through career development, on the job experiences and training opportunities.</li>
<li>Challenging work which supports the development of new and better ways to improve clinical outcomes for oncology treatment around the world.</li>
<li>An unwavering commitment to company values, employee safety and excellence in everything we do. &nbsp;</li>
</ul>
Diversity drives innovation; inclusion fosters belonging, growth and success. Sirtex believes that it takes multiple perspectives and voices to create a culture and workplace which fosters engagement, teamwork, and employee satisfaction to perform our best and deliver on commitments. We are dedicated to fostering an environment where all employees feel valued, included, and can share their ideas so that we can exceed even our own expectations.
Sirtex is An Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status, age or any other characteristic protected under applicable law.&nbsp; Sirtex will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.

Senior Product Development Engineer

<h3>Job Description</h3>
This is where you save and sustain lives 
At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You’ll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients.&nbsp;
Baxter’s products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered significant medical innovations that transform healthcare.
Together, we create a place where we are happy, successful and inspire each other. This is where you can do your best work.&nbsp;
Join us at the intersection of saving and sustaining lives— where your purpose accelerates our mission.&nbsp;
Your Role At Baxter
The Senior Manufacturing Engineer provides technical support to manufacturing operations, research and development projects, and facilities teams. They will be responsible for designing and developing equipment and tooling, collaborating with vendors, and owning key deliverables to support R&amp;D projects. Additionally, they will provide engineering support to manufacturing lines, conduct root cause analysis, and lead cross-functional projects. The ideal candidate will possess strong technical expertise, excellent communication skills, and a commitment to maintaining a clean and safe work environment, adhering to rigorous quality standards and cGMP regulations.
Your team:
We are a team of inquisitive individuals who embrace a collaborative environment to take on sophisticated challenges that meet the needs of our patients. We often need to change directions and respond to issues to avoid disruptions in our fast-paced manufacturing environment. Together, we build and maintain a positive work environment.
When you join us, you will work with a team of committed individuals who trust each other to deliver on the tasks at hand. We support innovation and out-of-the-box thinking balanced with collaboration across functions and other teams. Our leadership understands the need for continuous education and provides opportunities for further development.
What You'll Be Doing
<ul>
<li>Provide engineering support to manufacturing lines, including floor support, non-conforming product investigations, change order control requests reviews, and new equipment qualifications.</li>
<li>Design and develop equipment and tooling to support manufacturing processes</li>
<li>Collaborate with vendors to select and procure equipment and tooling</li>
<li>Own key deliverables in support of development and continuous/sustaining engineering R&amp;D projects, which may include:&nbsp;first articles, mold tool qualifications, component qualifications, process validations.&nbsp;</li>
<li>Work with Quality and R&amp;D engineers to prepare manufacturing work instructions, material specifications, and inspection documentation.&nbsp; Set inspection requirements, set inspection methods and inspection sampling plans.&nbsp;</li>
<li>Provide engineering support to the facilities and maintenance teams, including technical documentation, project management, equipment troubleshooting, and overall technical expertise.</li>
<li>Conduct root cause analysis and implement corrective actions as assigned.</li>
<li>Lead projects with cross-functional team members as assigned</li>
<li>Support internal audits and supplier audits.&nbsp;</li>
<li>Sustain a clean and safe work area using 6S principles</li>
<li>Learn, understand and apply rigorous quality standards, Standard Operating Procedures (SOPs) and Current Good Manufacturing Practices (cGMP)</li>
</ul>
What You'll Bring
<ul>
<li>B.S. degree in Engineering or Science (Biomedical Engineer, Chemical Engineer, Chemistry, Biochemistry, Materials Science, Electromechanics)&nbsp;</li>
<li>3+ years in an engineering role within a Medical Device company.&nbsp; Must have working experience of GMP and ISO 13485 requirements.&nbsp;</li>
<li>Ability to discuss normally encountered technical or project management issues, both verbally and in written form.</li>
<li>Ability to work as a collaborative team member.</li>
<li>Ability to solve routine design, engineering problems with assistance.</li>
<li>Effectively operate in a cross-functional team with guidance.</li>
<li>Must be able to provide solutions that reflect understanding business objectives and cost implications.</li>
<li>Ability to perform root cause analysis and problem solving.</li>
<li>Strong written and oral communication skills.</li>
<li>Working knowledge and understanding of mechanical drawings&nbsp;</li>
</ul>
<ul>
<li>Strong problem solving, technical writing, and statistical analysis skills&nbsp;</li>
</ul>
<ul>
<li>Experience with supporting a manufacturing product line&nbsp;</li>
</ul>
We understand compensation is an important factor as you consider the next step in your career. At Baxter, we are committed to equitable pay for all employees, and we strive to be more transparent with our pay practices. The estimated base salary for this position is $88,000 - $121,000 annually. The estimated range is meant to reflect an anticipated salary range for the position. We may pay more or less than of the anticipated range based upon market data and other factors, all of which are subject to change. Individual pay is based on upon location, skills and expertise, experience, and other relevant factors. This position may also be eligible for discretionary bonuses. For questions about this, our pay philosophy, and available benefits, please speak to the recruiter if you decide to apply and are selected for an interview.
Applicants must be authorized to work for any employer in the U.S. We are unable to sponsor or take over sponsorship of an employment visa at this time.
US Benefits at Baxter (except for Puerto Rico)
This is where your well-being matters. Baxter offers comprehensive compensation and benefits packages for eligible roles. Our health and well-being benefits include medical and dental coverage that start on day one, as well as insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance. Financial and retirement benefits include the Employee Stock Purchase Plan (ESPP), with the ability to purchase company stock at a discount, and the 401(k) Retirement Savings Plan (RSP), with options for employee contributions and company matching. We also offer Flexible Spending Accounts, educational assistance programs, and time-off benefits such as paid holidays, paid time off ranging from 20 to 35 days based on length of service, family and medical leaves of absence, and paid parental leave. Additional benefits include commuting benefits, the Employee Discount Program, the Employee Assistance Program (EAP), and childcare benefits. Join us and enjoy the competitive compensation and benefits we offer to our employees.&nbsp;For additional information regarding Baxter US Benefits, please speak with your recruiter or visit our Benefits site: Benefits | Baxter
Equal Employment Opportunity
Baxter is an equal opportunity employer. Baxter evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic.
Know Your Rights: Workplace Discrimination is Illegal
Reasonable Accommodations Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information.
Recruitment Fraud Notice Baxter has discovered incidents of employment scams, where fraudulent parties pose as Baxter employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information. To learn how you can protect yourself, review our Recruitment Fraud Notice.

Sr. Facilities Engineer

<h3>Job Description</h3>
Senior to Principal R&amp;D Engineer (Title Flexible)
Full-Time Permanent position
Incubator 5-Person Cardiovascular Medical Device Startup Company
Just closed Round A Financing
 
The Job: Early Design &amp; Development for class III Active Implantable device. Catheter-deployed Implant which combines various materials (Nitinol) &amp; Wireless Sensors.
 
Ideal Product Development Background/Experience: Active-Implants, electromechanical devices, Implants, ICD or Ultrasound 
 
Multiple Products taken from A-Z preferably.
 
Requirements:
BS or MS Engineering
5-10+ years medical device R&amp;D product development experience
Mix of Mechanical/Biomedical Engineering
Must Be Hands-On, as this is a startup and they need someone who can be very independent.
Local Candidates highly preferred
 
No H1B Candidates or Visa Sponsorships

Senior or Principal R&D Engineer - Active Implantable (Sensors, Transducers, Ultrasound)

<h3>Job Description</h3>
Job DescriptionSalary: 
Position Description
As Project Engineer, you will support the Product Development teams goal of improving patient outcomes by developing new implants, instruments, and surgical planning systems. You will be the owner of new product development and existing product improvement projects. You will have autonomy and be expected to identify solutions to problems on your own. In addition to developing and improving products, you will collaborate with peripheral groups including Operations, Quality, Regulatory, and Markeing as we build the first-in-industry, scalable patient-specific process. To be successful in this role, you must be a team-player, self-motivated, and invested in improving patient lives.
Responsibilities
<ul>
<li>Directly responsible for the development of new product and or the enhancement of existing products</li>
<li>Lead or serve as a member of project teams involved in novel implant, instrument, and surgical planning solutions</li>
<li>Creates and supports the development of prototypes and processes using in-house or external resources</li>
<li>Leverages CAD software to design medical devices and instruments suitable for a traditional, novel, and additive manufacturing methods</li>
<li>Specifies engineering drawings, including assignment of dimensions and tolerances to designs</li>
<li>Creates and maintains documentation relevant to design control and other applicable regulatory requirements</li>
<li>Documents technical assessments of mechanical design (eg FEA, tolerance analysis, testing, etc.)</li>
<li>Provides support to current and future products manufactured in house or by outside vendors</li>
<li>Supports cadaver labs during surgeon education events, including cadaver setup, running a fluoroscopy machine, clean-up, etc</li>
<li>Assists Regulatory team by providing documentation and technical support for FDA submissions</li>
<li>Provides engineering support to Manufacturing, Quality, Marketing, and Sales as necessary</li>
<li>Adheres to project delivery schedules and performs duties in compliance with applicable FDA and state regulations as well as standards including, but not limited to, ISO 13485</li>
</ul>
Qualifications
<ul>
<li>Education: Bachelors degree in Mechanical Engineering, Mechatronic Engineering, or Biomedical Engineering</li>
<li>Experience: 4-6 years of industry experience with a minimum of 2 years in medical device product development</li>
<li>Experience with spine or orthopedics highly desired</li>
<li>Demonstrated ability to lead product development from concept through product launch, including planning, organizing, and time management skills</li>
<li>Experience in project management methods applied to the medical device industry (scope definition, work breakdown structure, timeline generation and resourcing, timeline execution and reporting)</li>
<li>Solid understanding of traditional manufacturing methods for implants and instruments</li>
</ul>
 
Skills
<ul>
<li>Excellent verbal and written communication</li>
<li>Strong ability to write technical and business reports and correspondence</li>
<li>Strong mechanical design skills able to generate high-quality concepts quickly</li>
<li>Thorough and detail-oriented able to execute complex technical work without errors or need for rework</li>
<li>Willingness to wear multiple hats when needed to support Carlsmeds mission</li>
<li>Experience translating mechanical designs into manufacturable drawings/specifications and supporting designs throughout the design transfer process for successful product launches.</li>
<li>Strong ability to read and interpret documents such as drawings,safety rules, company policy and procedure manuals</li>
</ul>
 
Equal Opportunity Employer
Carlsmed is an equal opportunity employer. All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status. Carlsmed is committed to providing reasonable accommodations for candidates with disabilities in our recruiting process. If you need any assistance or accommodations due to a disability, please let us know. 
Compensation
We are pleased to provide a competitive salary and benefits. Our benefits reflect our investment in the overall health and well-being of our employees and their families. including paying 100% of monthly healthcare, dental &amp; vision insurance premiums, a 401(k) plan with employer matching and unlimited PTO. The expected pay range is: $110K to $125K annually. Compensation may vary based on related skills, experience, and relevant key attributes.

Project Engineer

<h3>Job Description</h3>
Job Description
Akkodis is seeking an RD Engineer for a contract job with a client in Maple Grove, MN. Candidates must have experience in implant design and development, along with CAD modeling and FEA simulation skills to be considered.
Rate Range: $37/hour to 49/hour; The rate may be negotiable based on experience, education, geographic location, and other factors.

RD Engineer job responsibilities include:
<ul>
<li>
Design and develop new products, materials, or processes for projects of moderate complexity, ensuring performance and quality standards.
</li>
<li>
Conduct engineering tests and experiments, analyze data, and prepare technical reports to support product development.
</li>
<li>
Troubleshoot design, material, or process issues and implement improvements based on test results and performance analysis.
</li>
<li>
Collaborate with cross-functional teams including quality, manufacturing, regulatory, and marketing to ensure project success.
</li>
<li>
Create and maintain engineering documentation, including specifications, tooling designs, and test protocols.
</li>
<li>
Contribute to innovation by generating new product or process concepts and submitting idea disclosures.
</li>
</ul>
Required Qualifications:
<ul>
<li>
Bachelor’s degree in mechanical, Biomedical, Chemical Engineering, or a related field (master’s preferred).
</li>
<li>
3–4 years with a BS or 1–2 years with an MS in relevant engineering discipline.
</li>
<li>
Proven experience in the design and development of medical implants.
</li>
<li>
Proficiency in CAD modeling, FEA simulations, and rapid prototyping.
</li>
</ul>
If you are interested in this role, then please click APPLY NOW. For other opportunities available at Akkodis, or any questions, feel free to contact me at Punit.Pathak@akkodisgroup.com
 Pay Details: $37.00 to $49.00 per hour Benefit offerings available for our associates include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, EAP program, commuter benefits and a 401K plan. Our benefit offerings provide employees the flexibility to choose the type of coverage that meets their individual needs. In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other paid leave required by Federal, State, or local law, as well as Holiday pay where applicable. Equal Opportunity Employer/Veterans/Disabled To read our Candidate Privacy Information Statement, which explains how we will use your information, please navigate to <a href="https://www.akkodis.com/en/us/candidate-privacy-policy" target="_blank">https://www.akkodis.com/en/us/candidate-privacy-policy</a> The Company will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or security clearance requirements, including, as applicable: 
<ul>
<li>The California Fair Chance Act</li>
<li>Los Angeles City Fair Chance Ordinance</li>
<li>Los Angeles County Fair Chance Ordinance for Employers</li>
<li>San Francisco Fair Chance Ordinance</li>
</ul>
 Company DescriptionGlobal Footprint, Local Impact: As part of the world's second-largest ER&amp;D company, you'll join a network of 50,000 professionals across 30 countries, each contributing to impactful projects worldwide while benefiting from a close-knit community at a local level. Diverse Career Paths: With services ranging from specialist recruitment to cloud infrastructure and sustainability, Akkodis offers a multitude of career paths. Whether you're a software developer, data analyst, or sustainability expert, there's a place for your skill set. Commitment to Innovation: Innovation is our cornerstone. With continuous investments in analytics and market intelligence, we not only predict the future of technology – we create it. Your ideas and innovations will have the space to flourish. Continuous Learning and Development: The Akkodis Academy offers unrivaled opportunities for learning and professional growth, ensuring you remain at the forefront of your field. Our culture values continuous improvement, both for our company and for your career. Inclusive and Collaborative Culture: We believe in the power of diverse perspectives and collaborative work environments. At Akkodis, you'll find a community where inclusivity drives innovation and where every voice is heard. Our Evolution and Your Role in It Akkodis emerged from the strategic merger of AKKA Technologies and Modis in 2023, under the Adecco Group. This fusion created a powerhouse in digital engineering and technology, blending European engineering finesse with global technological capabilities. As we write our next chapter, your skills and vision will be instrumental in driving our continued success. Empowering the Future We're not just creating solutions; we're empowering industries to be more efficient, sustainable, and forward-thinking. Our work in industrial automation, product development, and custom software solutions is setting new standards in technology and engineering. Join the Akkodis Community At Akkodis, you're more than just an employee – you're a vital part of a community shaping the future. We're excited to see where your expertise can take us. Discover where you fit in our diverse range of opportunities and start engineering a smarter future with us today. 
<h3>Company Description</h3>
Global Footprint, Local Impact: As part of the world's second-largest ER&amp;D company, you'll join a network of 50,000 professionals across 30 countries, each contributing to impactful projects worldwide while benefiting from a close-knit community at a local level.\r\n\r\nDiverse Career Paths: With services ranging from specialist recruitment to cloud infrastructure and sustainability, Akkodis offers a multitude of career paths. Whether you're a software developer, data analyst, or sustainability expert, there's a place for your skill set.\r\n\r\nCommitment to Innovation: Innovation is our cornerstone. With continuous investments in analytics and market intelligence, we not only predict the future of technology – we create it. Your ideas and innovations will have the space to flourish.\r\n\r\nContinuous Learning and Development: The Akkodis Academy offers unrivaled opportunities for learning and professional growth, ensuring you remain at the forefront of your field. Our culture values continuous improvement, both for our company and for your career.\r\n\r\nInclusive and Collaborative Culture: We believe in the power of diverse perspectives and collaborative work environments. At Akkodis, you'll find a community where inclusivity drives innovation and where every voice is heard.\r\n\r\nOur Evolution and Your Role in It\r\n\r\nAkkodis emerged from the strategic merger of AKKA Technologies and Modis in 2023, under the Adecco Group. This fusion created a powerhouse in digital engineering and technology, blending European engineering finesse with global technological capabilities. As we write our next chapter, your skills and vision will be instrumental in driving our continued success.\r\n\r\nEmpowering the Future\r\n\r\nWe're not just creating solutions; we're empowering industries to be more efficient, sustainable, and forward-thinking. Our work in industrial automation, product development, and custom software solutions is setting new standards in technology and engineering.\r\n\r\nJoin the Akkodis Community\r\n\r\nAt Akkodis, you're more than just an employee – you're a vital part of a community shaping the future. We're excited to see where your expertise can take us. Discover where you fit in our diverse range of opportunities and start engineering a smarter future with us today.

R&D Engineer

<h3>Job Description</h3>
Job DescriptionDescription:
At Esaote North America, we believe that technology is not truly state-of-the-art unless it serves real world needs. We understand the demands of today's clinical environments, and we continue to develop MRI and ultrasound systems that are user-friendly and patient-friendly, ergonomic and affordable. 
 
Esaote North America is seeking an experienced MRI Field Service Engineer to join our service team. This remote, field-based role provides technical support for Esaote MRI systems, including installation, preventive and corrective maintenance, troubleshooting, upgrades, and customer support. The ideal candidate will be based in the Atlanta area to support customers throughout the region, with potential national travel as needed.
What You’ll Do:
<ul>
<li>Perform on-site service, diagnostics, and repairs on Esaote MRI systems. </li>
<li>Install and commission MRI systems, ensuring quality and regulatory compliance. </li>
<li>Conduct preventive maintenance and safety checks. </li>
<li>Provide system operation training and support to customers. </li>
<li>Document service activities and communicate feedback to the service team. </li>
<li>Collaborate with engineering, technical support, and service leadership. </li>
</ul>
What We’re Looking For:
<ul>
<li>Associate or bachelor’s degree in Biomedical or Electrical Engineering (or related field); military-equivalent training considered. </li>
<li>3+ years of hands-on field service experience with diagnostic imaging equipment; MRI experience required (Esaote or open MRI strongly preferred). </li>
<li>Strong technical skills in MRI subsystems, networking/DICOM, and use of diagnostic equipment. </li>
<li>Ability to travel extensively (up to 75%) with overnight stays. </li>
<li>Valid driver’s license with clean record. </li>
<li>Must meet hospital credentialing requirements. </li>
</ul>
Preferred Certifications:
<ul>
<li>OEM MRI System Certification (Esaote or other) </li>
<li>AAMI CBET or CRES </li>
<li>OSHA 10/30 Safety Certification </li>
</ul>
Why Join Esaote: As part of a global leader in medical imaging, you’ll play a key role in supporting innovative MRI technology that makes a difference in healthcare. We offer a competitive compensation and benefits package, a collaborative culture, opportunities for professional growth, and the chance to represent a company known for quality and innovation. 
 
Esaote North America is an Equal Opportunity Employer and is committed to diversity, inclusion, and compliance with the ADA.
Requirements:

Field Service Engineer - MRI

<h3>Job Description</h3>
Job DescriptionDescription:
Summary: MM Solutions is a well-established company serving the Aerospace, Defense, Medical, and High-Tech Industries in Colorado specializing in custom packaging, professional services, custom cabling and logistic solutions. Creating opportunities and overcoming challenges is what drives us to provide clients with the necessary people, services, and equipment for every job. We are an organization that commits to its team members, maintaining a safe and fun environment while treating everyone as a valued individual.
 
We are an Equal Opportunity Employer, including disability and veteran status. Full benefits are available to full-time team members, including paid sick leave and vacation, medical/vision/dental, company-funded life insurance and 401(k).\
 
Position Summary: The Design Engineer contributes to the design, development, and continuous improvement of custom transport containers, cable harnesses, and mechanical assemblies supporting satellite and space programs. You will use industry-standard CAD software to produce detailed 3D models, drawings, and documentation, while also collaborating closely with our Operations team to improve manufacturability and tooling for production.
 
Design Engineers also work with Operations Team to support Production through process improvement and new production tools. Design engineers must overcome numerous technical (and other) hurdles to deliver a design that meets the outlined specifications with a strong attention to detail and a creative flair while maintaining good communication with internal and external teams.
 
 
Requirements:
Essential Job Function:
Design and Project Coordination for Large Design Projects
<ul>
<li>Design custom packaging and transportation solutions for various industries including biomedical and aerospace/defense</li>
<li>Conduct consultation and e-mail correspondence with clients to transition packaging concepts to drawings in a timely manner.</li>
<li>Generate documentation for production which includes design, cut lists, cost of material list and BOM’s</li>
<li>Generate job estimates and Develop Quotes in Salesforce. Present prototypes and designs to customers and internal teams</li>
<li>Prioritize tasks with input from Operations Engineer, develop functional designs that the operations team will utilize to build the finished product</li>
<li>Identify and source purchased items for projects and work with purchasing team to acquire components.</li>
<li>Identify new business opportunities based on customer needs</li>
</ul>
Production Support
<ul>
<li>Work a part of operations and engineering team to develop new products and processes to expand the company’s product lines</li>
<li>Develop improvements (jigs, fixtures, processes) to further lean manufacturing initiatives.</li>
<li>Collaborate with Customers, Sales, Scheduling and Production Departments (Crating, Case &amp; Foam and Cables).</li>
<li>Set up and Manage Maintenance Program for Production Equipment.</li>
<li>Cross train and work in other divisions/departments as needed</li>
<li>Demonstrate and apply our internal and external company values (aka "Anchors") by working positively and collaboratively with team members and customers to form good partnerships and great teams while innovating, eliminating the non-essential and improving.</li>
</ul>
 
Knowledge, Skills, and Abilities:
<ul>
<li>proficiency in SolidWorks (preferred) or AutoCAD, including 3D modeling, drawing creation, and file management; working knowledge of Microsoft Office applications; experience with Salesforce is a plus but not required.</li>
<li>Basic understanding of design safety standards and environmental considerations relevant to aerospace and industrial hardware.</li>
<li>Familiarity with Design for Manufacturability (DFM) and Geometric Dimensioning &amp; Tolerancing (GD&amp;T) principles, with the ability to apply them under supervision.</li>
<li>Ability to read, interpret, and create engineering drawings and assembly documentation in accordance with industry standards.</li>
<li>Strong analytical and problem-solving skills, using logic and structured thinking to evaluate alternatives and recommend solutions.</li>
<li>Effective planning and organizational skills, with the ability to prioritize tasks and manage multiple assignments to meet deadlines.</li>
<li>Professional communication and customer service orientation, including active listening and responsiveness to internal and external stakeholder needs.</li>
<li>High attention to detail and accuracy, with a commitment to following procedures and maintaining high-quality documentation.</li>
<li>Basic machining or fabrication knowledge (hands-on experience from coursework, internships, or personal projects is a plus).</li>
<li>Willingness to learn and follow manufacturing processes, quality controls, and applicable industry regulations, including ISO 9001:2015, AS9100, and (where applicable) ISO 13485.</li>
</ul>
 
Education and Experience preferred:
<ul>
<li>Bachelor’s degree in Mechanical Engineering, Engineering Technology, or a closely related field.</li>
<li>Interest in structural design, mechanical hardware, or packaging for high-value aerospace or industrial applications.</li>
<li>Good working knowledge of SolidWorks/AutoCAD, machining, and fabrication techniques.</li>
</ul>
 
Additional Requirements:
<ul>
<li> Employer is a drug-free workplace, and candidate must pass a pre-hire background check and drug screen. We do not discriminate in hiring on any basis, including citizenship, and our job postings are open to U.S. citizens as well as non-U.S. citizens. However, the person hired will have access to information and items protected under the International Traffic in Arms Regulation (ITAR), and therefore that person must be a “U.S. person” as that term is defined under ITAR, 22 CFR 120.15.</li>
<li>A “U.S. person is defined as a 1) U.S. Citizen, 2) a lawful permanent resident, 3) a refugee given asylum in the U.S., or 4) a temporary resident granted amnesty. Accordingly, it will be necessary for our company to confirm and verify your status as a “U.S. person” under ITAR at the time of hire.</li>
</ul>

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