field_job_employment_type

field_job_occupational_field_parents_all

job_organization_name

city

state

<h3>Job Description</h3>
Job Description
Ready to simulate success? Join our innovative team!
Are you a problem-solver who thrives on tackling complex engineering challenges? Do you geek out over the power of simulation tools like Ansys to bring ideas to life? If so, we want you to be part of our cutting-edge team!
At OsteoCentric Technologies, we’re redefining what’s possible. As a Simulation Engineer, you’ll have the opportunity to shape the future, working on groundbreaking projects that make a real impact. With access to state-of-the-art tools, a collaborative team of experts, and an environment that values innovation, this is your chance to flex your technical muscles and take your career to the next level.
The Simulation Engineer is responsible for performing advanced simulation and analysis using Ansys software (Mechanical, Motion, LS-DYNA, or optiSLang) to support product design and development. They will perform complex simulations, analyze results, and offer optimization recommendations for OsteoCentric products in the Medical Device and Industrial spaces. This role requires a proactive, collaborative engineer with experience in finite element analysis (FEA), dynamic modeling, or optimization processes, capable of working cross-functionally to drive innovation and product quality. This position is required to work in our North Austin office.
In this role you will:
<ul>
<li>Develop, set up, and execute simulation models using Ansys Mechanical, Ansys Motion, Ansys LS-DYNA, or Ansys optiSLang, depending on project requirements.</li>
<li>Perform finite element analysis (FEA) for structural, thermal, and/or dynamic simulations, and provide insights for design improvements.</li>
<li>Collaborate with design, R&amp;D, and product development teams to define simulation requirements and translate them into functional models.</li>
<li>Analyze and interpret simulation results, generating comprehensive reports to inform engineering and design decisions.</li>
<li>Conduct sensitivity and optimization studies using Ansys tools to ensure robustness and reliability in product design.</li>
<li>Troubleshoot and validate models to ensure accuracy and alignment with real-world testing and performance.</li>
<li>Participate in product testing and validation to correlate simulation data with physical data.</li>
<li>Stay current with advances in simulation technology and incorporate new methodologies to enhance simulation capabilities.</li>
<li>Prepare, deliver, and support technical presentations, publications, and IP filings based on the learnings from simulations, for both internal and external audiences. </li>
<li>Function as simulation Subject Matter Expert (SME), including training others on the mechanics and use of simulation tools, administrating and coordinating licenses and subscriptions, and recommending appropriate hardware. </li>
<li>Perform special projects and other duties as assigned.</li>
</ul>
Required Skills/Abilities:
<ul>
<li>Strong understanding of finite element analysis (FEA) and dynamic modeling principles.</li>
<li>Proficiency in developing, validating, and optimizing complex simulation models.</li>
<li>Familiarity with multi-physics simulation, particularly structural, thermal, and/or dynamic analyses.</li>
<li>Knowledge of scripting languages (e.g., Python) and familiarity with CAD software (e.g. SolidWorks).</li>
<li>Strong analytical, problem-solving, and decision-making abilities.</li>
<li>Excellent verbal and written communication skills, with the ability to create clear and actionable reports.</li>
<li>Collaborative team player with a proactive, self-driven work ethic.</li>
</ul>
Minimum Qualifications:
<ul>
<li>Bachelor’s degree in Mechanical Engineering, Aerospace Engineering, or Biomedical Engineering (with Mechanical concentration) from an accredited institution. Graduate degrees and certificates are preferred.</li>
<li>Minimum of 5 years of experience in engineering simulation, specifically with Ansys tools.</li>
<li>Proven expertise in at least one of the specified Ansys software systems: Ansys Mechanical, Ansys Motion, Ansys LS-DYNA, or Ansys optiSLang. Ansys certification/credentials preferred.</li>
</ul>
About Us:
UnifiMI Industrial was founded in 2024 and is a wholly-owned subsidiary of OsteoCentric Technologies. OsteoCentric was founded in 2015 to design, develop and innovate new advanced medical device technologies. Our flagship UnifiMI technologies have revolutionized the implant to bone interface utilizing both patented minimally invasive bone preparation technology and unique next-generation thread geometries. Our goal is to leverage MIS technology to significantly improve and accelerate a patient’s path to recovery. Our two state-of-the-art global innovation headquarters are located in Austin, Texas and Logan, Utah.
Fun facts about us:
<ul>
<li>70+ patents globally</li>
<li>100,000+ surgical implants used</li>
<li>Devices in 90+ level one trauma centers</li>
<li>20 FDA Clearances and counting</li>
<li>11 Commercialized Products</li>
<li>And this is just the beginning!</li>
</ul>
Compensation: Compensation will be determined based on experience and qualifications.
Benefits:
<ul>
<li>Significant employer contributions to Health, Vision, and Dental plans</li>
<li>A fully employer-sponsored life insurance plan</li>
<li>Voluntary: Additional Life/AD&amp;D Insurance, Long Term Disability, Short-Term Disability, Accident Insurance, Critical Illness Insurance, and Hospital Indemnity Insurance</li>
<li>401(k) Plan</li>
<li>15 days of Paid Time Off (PTO)</li>
<li>10 Holidays + 2 Floating Holidays of your choice</li>
<li>Employee recognition and development</li>
</ul>
Disclaimers: 
<ul>
<li>We do not accept applications from third-party recruiters or staffing agencies.</li>
<li>At this time, we are unable to sponsor work visas. Applicants must have authorization to work in the United States without sponsorship.</li>
</ul>

Simulation Engineer

<h3>Job Description</h3>
Job Description
Ready to simulate success? Join our innovative team!
Are you a problem-solver who thrives on tackling complex engineering challenges? Do you geek out over the power of simulation tools like Ansys to bring ideas to life? If so, we want you to be part of our cutting-edge team!
At OsteoCentric Technologies, we’re redefining what’s possible. As a Simulation Engineer, you’ll have the opportunity to shape the future, working on groundbreaking projects that make a real impact. With access to state-of-the-art tools, a collaborative team of experts, and an environment that values innovation, this is your chance to flex your technical muscles and take your career to the next level.
The Simulation Engineer is responsible for performing advanced simulation and analysis using Ansys software (Mechanical, Motion, LS-DYNA, or optiSLang) to support product design and development. They will perform complex simulations, analyze results, and offer optimization recommendations for OsteoCentric products in the Medical Device and Industrial spaces. This role requires a proactive, collaborative engineer with experience in finite element analysis (FEA), dynamic modeling, or optimization processes, capable of working cross-functionally to drive innovation and product quality. This position is required to work in our Logan, UT office.
In this role you will:
<ul>
<li>Develop, set up, and execute simulation models using Ansys Mechanical, Ansys Motion, Ansys LS-DYNA, or Ansys optiSLang, depending on project requirements.</li>
<li>Perform finite element analysis (FEA) for structural, thermal, and/or dynamic simulations, and provide insights for design improvements.</li>
<li>Collaborate with design, R&amp;D, and product development teams to define simulation requirements and translate them into functional models.</li>
<li>Analyze and interpret simulation results, generating comprehensive reports to inform engineering and design decisions.</li>
<li>Conduct sensitivity and optimization studies using Ansys tools to ensure robustness and reliability in product design.</li>
<li>Troubleshoot and validate models to ensure accuracy and alignment with real-world testing and performance.</li>
<li>Participate in product testing and validation to correlate simulation data with physical data.</li>
<li>Stay current with advances in simulation technology and incorporate new methodologies to enhance simulation capabilities.</li>
<li>Prepare, deliver, and support technical presentations, publications, and IP filings based on the learnings from simulations, for both internal and external audiences. </li>
<li>Function as simulation Subject Matter Expert (SME), including training others on the mechanics and use of simulation tools, administrating and coordinating licenses and subscriptions, and recommending appropriate hardware. </li>
<li>Perform special projects and other duties as assigned.</li>
</ul>
Required Skills/Abilities:
<ul>
<li>Strong understanding of finite element analysis (FEA) and dynamic modeling principles.</li>
<li>Proficiency in developing, validating, and optimizing complex simulation models.</li>
<li>Familiarity with multi-physics simulation, particularly structural, thermal, and/or dynamic analyses.</li>
<li>Knowledge of scripting languages (e.g., Python) and familiarity with CAD software (e.g. SolidWorks).</li>
<li>Strong analytical, problem-solving, and decision-making abilities.</li>
<li>Excellent verbal and written communication skills, with the ability to create clear and actionable reports.</li>
<li>Collaborative team player with a proactive, self-driven work ethic.</li>
</ul>
Minimum Qualifications:
<ul>
<li>Bachelor’s degree in Mechanical Engineering, Aerospace Engineering, or Biomedical Engineering (with Mechanical concentration) from an accredited institution. Graduate degrees and certificates are preferred.</li>
<li>Minimum of 5 years of experience in engineering simulation, specifically with Ansys tools.</li>
<li>Proven expertise in at least one of the specified Ansys software systems: Ansys Mechanical, Ansys Motion, Ansys LS-DYNA, or Ansys optiSLang. Ansys certification/credentials preferred.</li>
</ul>
About Us:
UnifiMI Industrial was founded in 2024 and is a wholly-owned subsidiary of OsteoCentric Technologies. OsteoCentric was founded in 2015 to design, develop and innovate new advanced medical device technologies. Our flagship UnifiMI technologies have revolutionized the implant to bone interface utilizing both patented minimally invasive bone preparation technology and unique next-generation thread geometries. Our goal is to leverage MIS technology to significantly improve and accelerate a patient’s path to recovery. Our two state-of-the-art global innovation headquarters are located in Austin, Texas and Logan, Utah.
Fun facts about us:
<ul>
<li>70+ patents globally</li>
<li>100,000+ surgical implants used</li>
<li>Devices in 90+ level one trauma centers</li>
<li>20 FDA Clearances and counting</li>
<li>11 Commercialized Products</li>
<li>And this is just the beginning!</li>
</ul>
Compensation: Compensation will be determined based on experience and qualifications.
Benefits:
<ul>
<li>Significant employer contributions to Health, Vision, and Dental plans</li>
<li>A fully employer-sponsored life insurance plan</li>
<li>Voluntary: Additional Life/AD&amp;D Insurance, Long Term Disability, Short-Term Disability, Accident Insurance, Critical Illness Insurance, and Hospital Indemnity Insurance</li>
<li>401(k) Plan</li>
<li>15 days of Paid Time Off (PTO)</li>
<li>10 Holidays + 2 Floating Holidays of your choice</li>
<li>Employee recognition and development</li>
</ul>
Disclaimers: 
<ul>
<li>We do not accept applications from third-party recruiters or staffing agencies.</li>
<li>At this time, we are unable to sponsor work visas. Applicants must have authorization to work in the United States without sponsorship.</li>
</ul>

<h3>Job Description</h3>
Job Description
 
MoFe Engineer
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>
</ul>
<ul>
<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.
 
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: 60000-70000 Yearly Salary
 
PIa05658567c11-25405-38327992

MoFe Engineer

<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
 
PI31e992a62088-25405-38089402

MoFe Engineer I

<h3>Job Description</h3>
Job Description
Description
Verista's 500 experts team up with the world's most recognizable brands in the life science industry to solve their business needs. The nature of our business is to empower growth and innovation within the scientific community and to help researchers, organizations, and companies solve some of the world's most pressing healthcare challenges. Verista provides innovative solutions and services that empower informed decision-making and are the result of our significant investment in our people and our capabilities.
Our ability to grow is driven by world-class people who thrive in a team environment and share our mission to enable life sciences clients to improve lives. Our talented and dedicated professionals are committed to making an impact every day.
Company Culture Guidelines &amp; Values:
<ul>
<li>We empower and support our colleagues</li>
<li>We commit to client success at every turn</li>
<li>We have the courage to do the right thing</li>
<li>We encourage an inclusive environment where our colleagues feel respected, engaged, and challenged.</li>
<li>We constantly acquire new skills and learn from our experiences to enhance our collective expertise</li>
</ul>
CQV Engineer Responsibilities (Typical):
<ul>
<li>Managing and working collaboratively with clients' quality representative to complete deviation investigation and resolution for problems and issues encountered during execution activities. Includes ability to complete root cause analysis</li>
<li>Supporting clients change management program – including authoring proposed changes, executing impact assessments/ regression analysis, and supporting client documentation of change results and release</li>
<li>Authoring, editing, and executing technical commissioning, qualification and validation documentation for standard equipment/systems/ software, and processes as part of team as directed by the project leader</li>
<li>Running test scripts and documenting results</li>
<li>Adherence with project schedule for all assigned activities</li>
<li>Maintaining clear, detailed records qualification and validation</li>
<li>Documenting impact and risk assessments as part of a team</li>
<li>Completing user interface testing, software verification, and complete alarm testing on automated systems</li>
<li>Developing, reviewing, and executing testing documentation</li>
<li>Making recommendations for design or process modification based on test results when executing test scripts</li>
<li>Reading technical schematics to identify, locate, and test photo sensors, verify part numbers, and complete I/O testing on automated manufacturing equipment</li>
<li>General understanding of capital equipment implementation and process knowledge</li>
<li>Understanding validation documents, URS, IQ, OQ, PQ</li>
<li>Verifying system drawings including ability to review and as-built P&amp;IDs (piping and instrumentation drawings) and I&amp;C (instrumentation and controls) drawings as well as verifying electrical schematics with support of an electrical engineer</li>
</ul>

Requirements:
<ul>
<li>Must be able to meet onsite work requirements in Holly Springs, NC</li>
<li>Bachelor's Degree or equivalent required (STEM degree, Biomedical Engineering, Chemical Engineering preferred)</li>
<li>2-4 years of relevant industry experience</li>
<li>Proficiency using PC and Microsoft Office tools</li>
<li>Outgoing personality with strong ability to communicate effectively with peers in clear, concise terms</li>
<li>Ability to work as part of a team</li>
<li>Strong problem-solving and critical thinking skills</li>
<li>Excellent organizational and time management skills</li>
<li>Strong attention to detail</li>
<li>GMP and Good Documentation Practice training (may be completed at onboarding)</li>
<li>Intermediate skills with WORD (authoring/editing large technical documents with styles, tables, TOCs, track changes)</li>
<li>Basic skills with EXCEL and PowerPoint</li>
<li>Strong interpersonal skills and clear communication capabilities</li>
</ul>
For US geography, the salary range for this position is shown below. The actual salary is dependent upon a variety of job-related factors such as professional background, training, work experience, location, business needs, market demand, and competitive market practice. Therefore, in some circumstances, the actual salary could fall outside of this expected range. This salary range is subject to change and may be modified in the future.
*Verista is an equal opportunity employer.
National (US) Range$65,000—$104,439 USD
Benefits
Why Choose Verista?
<ul>
<li>High growth potential and fast-paced organization with a people-focused culture</li>
<li>Competitive pay plus performance-based incentive programs</li>
<li>Company-paid Life, Short-Term, and Long-Term Disability Insurance.</li>
<li>Medical, Dental &amp; Vision insurances</li>
<li>FSA, DCARE, Commuter Benefits</li>
<li>Supplemental Life, Hospital, Critical Illness and Legal Insurance</li>
<li>Health Savings Account</li>
<li>401(k) Retirement Plan (Employer Matching benefit)</li>
<li>Paid Time Off (Rollover Option) and Holidays</li>
<li>As Needed Sick Time</li>
<li>Tuition Reimbursement</li>
<li>Team Social Activities (We have fun!)</li>
<li>Employee Recognition</li>
<li>Employee Referral Program</li>
<li>Paid Parental Leave and Bereavement</li>
</ul>
Verista collects and processes personal data in accordance with applicable data protection laws. If you are a California Job Applicant, see the privacy notice for further details. 
For more information about our company, please visit us at Verista.com

5832- CQV Engineer / Validation Engineer 2

<h3>Job Description</h3>
Job Description
Job Title: Systems Engineer 1-(Engineer -Degreed-II)
Location:St. Paul, MN 55117 – Onsite 
Duration: 12 months contract with possible extension
Shift/Schedule: 8:00 AM -5:00 PM/M-F
Pay Rate/Range: $40.00/hr on W-2 through Select Source International
Job Summary:
We are seeking a motivated and curious Systems Engineer to join our Systems Verification team. This role offers a unique opportunity to contribute to cutting-edge projects in motion control and robotics while developing your engineering skills in a collaborative and fast-paced environment. You’ll work alongside experienced engineers and gain hands-on experience in testing, data analysis, and system validation.
Key Responsibilities:
<ul>
<li>Execute system-level tests and analyze results to support product development.</li>
<li>Assist in developing and validating test methods for motion control and robotic systems.</li>
<li>Contribute to fixture design using ECAD/MCAD tools.</li>
<li>Support cross-functional engineering efforts (EE/HW/SW).</li>
<li>Write scripts and tools using LabVIEW and Python to automate testing and data collection.</li>
<li>Document test procedures, results, and findings clearly and accurately.</li>
</ul>
Additional Responsibility:
<ul>
<li>Collaborate with senior engineers on test planning and execution.</li>
<li>Participate in design and requirements reviews.</li>
<li>Learn and apply FDA regulatory and ISO standard procedures.</li>
<li>Engage in process improvement initiatives and technical reviews.</li>
</ul>
Qualifications:
<ul>
<li>Bachelor’s degree in engineering (Electrical, Software, Mechanical, or Biomedical) or related field.</li>
<li>Basic understanding of system testing and development lifecycle.</li>
<li>Strong verbal and written communications with ability to effectively communicate at multiple levels in the organization</li>
<li>Ability to work within a team and as an individual contributor in a fast-paced, changing environment.</li>
<li>Ability to multitasks, prioritizes, and meets deadlines in timely manner.</li>
<li>Strong organizational skills and attention to detail.</li>
</ul>
Preferred Experience:
<ul>
<li>Prior experience performing design verification testing.</li>
<li>Exposure to medical device development or regulated environments is beneficial but not required.</li>
<li>Familiarity with programming (LabVIEW, Python) and design tools (Altium, SolidWorks) is a plus.</li>
</ul>
Company DescriptionSelect Source International (SSI) is a distinguished staffing company with nearly 25 years of experience, renowned for delivering top-tier workforce solutions encompassing staffing, recruiting, and managed services. As a proud supplier, we bring a wealth of expertise and best-in-business differentiators to comprehensively support your diverse workforce needs. Based in Minneapolis, Minnesota, USA, SSI has established itself as a global leader, serving a broad clientele across industries with unwavering dedication and excellence. SSI is ISO 9001, 14001, and Soc2 Type2 certified, underscoring our commitment to quality and security. We have garnered numerous sustainability and supplier diversity awards, further validating our industry-leading capabilities 
<h3>Company Description</h3>
Select Source International (SSI) is a distinguished staffing company with nearly 25 years of experience, renowned for delivering top-tier workforce solutions encompassing staffing, recruiting, and managed services. As a proud supplier, we bring a wealth of expertise and best-in-business differentiators to comprehensively support your diverse workforce needs.\r\n\r\nBased in Minneapolis, Minnesota, USA, SSI has established itself as a global leader, serving a broad clientele across industries with unwavering dedication and excellence. SSI is ISO 9001, 14001, and Soc2 Type2 certified, underscoring our commitment to quality and security. We have garnered numerous sustainability and supplier diversity awards, further validating our industry-leading capabilities

System Engineer

<h3>Job Description</h3>
Job DescriptionJob Title: Manufacturing Engineer Company: VistaApex Solutions Location: Racine, Wisconsin (Corporate Headquarters) Reports to: Director of Operations About VistaApex Solutions VistaApex Solutions is a purpose-driven, clinician-focused healthcare platform bringing together leading dental brands, including Vista Apex, PerioProtect, and PerioSciences. Our mission is to develop meaningful products that enhance clinicians’ treatment options and improve patient outcomes. With a value-added approach across R&amp;D, operations, and customer experience.&nbsp; We empower clinicians to deliver confident, consistent, and elevated care. At our core, we operate through five foundational pillars— Product Development + Clinician Involvement, Treatment Refinement + Simplified Workflow, Expanding Innovations + Trusted Partnerships, Inspired Foresight and Quality Assured + Personal Connections —guiding our approach to innovation, collaboration, and long-term partnership. Position Overview The Manufacturing Engineer plays a critical role in driving continuous improvement across VistaApex’s operations. This position is responsible for identifying and implementing opportunities to enhance product value, reduce costs, and improve overall performance through systematic analysis and sound engineering practices. A key responsibility of this role is to strengthen the vendor base for VistaApex. This includes identifying and onboarding new suppliers, either domestically within the United States or in international regions with favorable tariff structures. The Manufacturing Engineer will also support the integration and commissioning of new equipment at the VistaApex facility to support production and operational efficiency. This role collaborates closely with cross-functional teams, including design, sourcing, and supply chain, to ensure alignment of manufacturing initiatives with overall business objectives. Key Functions
<ul>
<li>Determines company product manufacturing needs and provides technical resources to accomplish a smooth transition within the manufacturing environment. Handling the handoff from project design to manufacturability and automating</li>
<li>Conduct thorough value analysis and engineering assessments on existing and new products to identify cost-saving opportunities and performance improvements.</li>
<li>Collaborate with design and manufacturing teams to implement effective design changes and material substitutions.</li>
<li>Lead workshops and brainstorming sessions to generate innovative ideas for product enhancements.</li>
<li>Analyze product lifecycle costs and provide recommendations to optimize value throughout the product development process.</li>
<li>Monitor and evaluate the effectiveness of implemented changes, providing feedback for continuous improvement.</li>
<li>Stay updated on industry trends and best practices in value engineering and product development.</li>
<li>Conduct comprehensive value analysis and engineering assessments on existing and new products to identify significant cost-saving opportunities and performance enhancements.</li>
<li>Lead the qualification and onboarding process for new vendors, ensuring alignment with company standards and strategic goals.</li>
<li>Solves problems associated with manufacturing fallout and system bottlenecks</li>
<li>Plans for the arrangement of machines within the plant facilities to ensure the most efficient production processing layout</li>
<li>Installation of automated equipment for tip manufacturing and kitting improvements</li>
<li>Plant Layout analysis while new business is onboarded</li>
<li>Open molds or identify new pieces of equipment to bring production of appropriate SKUs in house. Assist with the set-up of equipment and training personnel. </li>
<li>Identify and onboard new vendors in the United States and countries with lower tariffs to the United States to mitigate the current supply chain exposure.</li>
<li>Analyze dual source and dual path options for highest spend SKUs, to determine if it makes sense to bring production in house and to have multiple options in different countries.</li>
<li>Drive cost savings or cost avoidance initiatives for each SKU.</li>
<li>Push internal documentation through Vista Apex Change Control Process to qualify and approve new vendors.</li>
<li>Develop drawings, Receiving Inspection Reports, and other documentation needed for change management.</li>
<li>Other duties as assigned</li>
</ul>
The above statements are intended to describe the general nature and level of work being performed. They are not intended to be construed as an exhaustive list of all responsibilities, duties, and skills required. Job Requirements
<ul>
<li>Bachelor’s degree in Engineering (Mechanical, Industrial, Biomedical, or related field) or equivalent experience; Master’s degree is a plus.</li>
<li>Proven experience in manufacturing engineering, preferably in a medical manufacturing environment.</li>
<li>Experience with product development and strong project management skills, including the ability to manage multiple projects simultaneously.</li>
<li>Proficient in Microsoft Office, particularly Excel; experience with Microsoft Project is helpful.</li>
<li>Proficient in engineering tools and software, such as CAD and other relevant technical applications.</li>
<li>Strong analytical and problem-solving skills, with a focus on cost reduction and performance improvement.</li>
<li>Excellent communication and interpersonal skills, with the ability to work collaboratively across teams.</li>
<li>Familiarity with lean manufacturing principles and continuous improvement methodologies is a plus.</li>
<li>Experience onboarding new vendors in previous roles is a plus.</li>
</ul>
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 accommodation may be made to enable individuals with disabilities to perform the essential functions.
<ul>
<li>While performing the duties of this job, the employee is frequently required to sit; use hands to finger, handle, or touch objects; and talk or hear. The employee is occasionally required to stand, walk, climb or balance, and taste or smell. The employee must frequently lift and/or move up to 10 pounds. Specific vision abilities required by this job include close vision, distance vision, color vision, depth perception, and the ability to adjust focus.</li>
</ul>
Work Environment The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions.
<ul>
<li>The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions.</li>
<li>The position is an office-based position.</li>
<li>Fast-paced, dynamic environment requiring adaptability and proactive communication.</li>
</ul>
Benefits We believe in supporting our employees both inside and outside of work. Here’s what you can expect when you join our team:
<ul>
<li>Comprehensive Health Coverage: Medical, dental, and vision insurance for you and your dependents.</li>
<li>Time Off: Generous PTO policy and paid holidays</li>
<li>Retirement Plans: 401(k) with company matching to help you plan for the future.</li>
<li>Wellness Support: Mental health resources and wellness programs.</li>
<li>Team Connection: Regular team events, retreats, and gatherings to build community.</li>
</ul>
 &nbsp;
Powered by JazzHR
JFTaldOj50

Manufacturing Engineer

<h3>Job Description</h3>
Job DescriptionBenefits: 
<ul>
<li>401(k)</li>
<li>401(k) matching</li>
<li>Dental insurance</li>
<li>Health insurance</li>
<li>Paid time off</li>
<li>Vision insurance</li>
</ul>
 Optical Applications Engineer (Remote) Job Description: Avantier Inc., a premium high-precision custom optics manufacturer and innovative imaging solutions provider, is seeking an experienced Optical Applications Engineer to join our growing team. This is an exciting opportunity to deliver high-precision custom optical solutions to clients across industries such as AR/VR, Life Sciences, Biomedical, Aerospace, and more. This position offers the flexibility to work primarily from home, with occasional travel to our New Jersey office, customer meetings, and industry trade shows. The ideal candidate will have a minimum of five years of experience, strong communication skills, and a customer-focused approach. Key Responsibilities: 
<ul>
<li>Develop and support optical design solutions for prototypes and proof-of-concept models.</li>
<li>Lead optical design and engineering efforts for new customer projects.</li>
<li>Collaborate with customers, the Sales team, and Sales Engineers to drive project success.</li>
<li>Assist the Sales team during technical calls with engineers.</li>
<li>Design and optimize optical systems using Zemax.</li>
<li>Develop and manage the production of marketing materials (online, electronic, video, and print).</li>
<li>Create and deliver training materials for the Sales team and onboard new engineering team members.</li>
<li>Work closely with the marketing team on product launches and existing product enhancements.</li>
<li>Prioritize and manage multiple projects simultaneously.</li>
</ul>
 Requirements: 
<ul>
<li>Minimum of 5 years of experience in optical engineering, opto-mechanical systems, optical assembly, or optical metrology.</li>
<li>Expertise in optical lens fabrication, plastic optical materials, complex optical system designs, and tolerance analyses.</li>
<li>Proficiency in sequential and non-sequential ray tracing.</li>
<li>Strong knowledge of optical simulation software such as Zemax, CodeV, or LightTools.</li>
<li>Proven ability to perform comprehensive system-level performance analyses and develop detailed optical system specifications.</li>
<li>Deep understanding of the complete production lifecycle, from design to manufacturing.</li>
<li>Excellent written and verbal communication skills.</li>
</ul>
Education: 
<ul>
<li>Bachelor's Degree (Required) 
<ul>
<li>Major: Optical Engineering, Physics, Electrical Engineering, Mechanical Engineering or a related technical field. </li>
</ul>
</li>
<li>Minimum Experience: 5 years of hands-on experience in optical design, product development, or applications engineering.</li>
</ul>
 Required Skills: 
<ul>
<li>Experience with SolidWorks and AutoCAD.</li>
<li>Strong analytical and problem-solving abilities.</li>
</ul>
Compensation &amp; Benefits: 
<ul>
<li>Salary: $90-120K + bonus.</li>
<li>Benefits: Health, dental, and vision insurance, along with a 401(k) plan.</li>
</ul>
 
This is a remote position.

Optical Applications Engineer

<h3>Job Description</h3>
Job DescriptionAbout ASG
ASG specializes in the development, qualification, and commercialization of drug delivery systems for biomedical products. We deliver integrated business and science solutions to foster healthier, safer, and more prosperous communities. Guided by our core values—service, client success, curiosity, respect, integrity, and accountability—we value diversity and prioritize collaboration and growth within our inclusive, team-oriented culture.&nbsp;&nbsp;Check out our&nbsp;GOASG&nbsp;website.&nbsp;
Test Engineer (Level 2) Summary
We are looking for a Test Engineer&nbsp;experienced in lab testing, test equipment development, and verification methodologies. You will operate independently with minimal supervision and contribute to the technical rigor and collaborative culture at ASG. This role requires both technical depth and strong communication skills to support team and project goals.
Key ResponsibilitiesTesting &amp; Methodology
<ul>
<li>
Design, develop, and implement custom test equipment, fixturing, and instrumentation.
</li>
<li>
Translate system requirements and specifications into formalized test methods.
</li>
<li>
Perform standard device testing (e.g., DOE, GR&amp;R) and data characterization.
</li>
<li>
Execute testing protocols with precision and accuracy.
</li>
<li>
Draft and revise technical documentation, including methods and test scripts.
</li>
<li>
Review test results for quality and compliance.
</li>
</ul>
Safety &amp; Standards
<ul>
<li>
Comply with all applicable industry and client safety procedures and training.
</li>
<li>
Apply relevant industry and client standards.
</li>
<li>
Adhere to ALCOA (Attributable, Legible, Contemporaneous, Original, Accurate) principles.
</li>
</ul>
Preparation &amp; Organization
<ul>
<li>
Coordinate materials, traceability, and supply readiness with engineering teams.
</li>
<li>
Track and maintain test documentation, materials, issues, and schedules.
</li>
</ul>
Communication &amp; Reporting
<ul>
<li>
Present and communicate testing results and issues clearly to stakeholders.
</li>
<li>
Actively contribute to technical team knowledge and verification practices.
</li>
</ul>
Data Analysis &amp; Statistics
<ul>
<li>
Apply foundational statistical methods in test analysis.
</li>
<li>
Ensure integrity and traceability of all collected test data.
</li>
</ul>
Leadership and Team Development
<ul>
<li>
Contribute to a culture of continuous learning through personal and team development plans.
</li>
</ul>
Qualifications
<ul>
<li>
Bachelor’s degree in Engineering or a related technical discipline.
</li>
<li>
5+ years of experience in a technical or engineering role, preferably involving lab testing.
</li>
</ul>
Knowledge, Skills, and Abilities
<ul>
<li>
Proficient knowledge of lab testing principles, mechanical device testing, and Zwick Roell systems.
</li>
<li>
Ability to define and verify test steps and cases based on design and stakeholder needs.
</li>
<li>
Understanding of measurement uncertainty and engineering fundamentals.
</li>
<li>
Strong analytical reasoning, problem-solving, and troubleshooting capabilities.
</li>
<li>
Effective communication and collaborative teamwork skills.
</li>
<li>
Time management and organizational ability in a fast-paced environment.
</li>
</ul>
Behaviors: Core Values
<ul>
<li>
Accountability: Owning the consequences of your decisions and actions.
</li>
<li>
Integrity: Complete harmony in what you think, say, and do concerning the ASG Way and our Code of Conduct.
</li>
<li>
Respect: Treating people the way you want to be treated, whether or not you agree with them.
</li>
<li>
Curiosity: An enduring desire to learn and grow.
</li>
<li>
Client Service: Results that address client needs based on client decisions.
</li>
<li>
Service: Giving priority to enriching the lives of others.
</li>
</ul>
Powered by JazzHR
h3T6aOAVMv

Test Engineer

<h3>Job Description</h3>
Job DescriptionDescription:
This position is an in-person role at our El Dorado Hills, CA headquarters. Interested? Please visit our careers website at shalbytech.com/careers for additional information.
 
As a Product Development Engineer, your role will be to creatively address project related design issues and lead development feasibility/concept work on new development projects. You will be responsible for the design conceptualization of new product ideas; creative problem solving; and facilitation of product development activities such as design and coordination of prototypes, evaluation of new concepts, solid modeling and drafting, participation in brainstorming and other team activities, and coordination of mechanical testing as required.
 
Duties/Responsibilities
<ul>
<li>Perform all engineering elements of our Quality Management System, including: </li>
<li>Design Controls </li>
<li>Risk Analyses, DFMEA</li>
<li>Design History Files (DHF)</li>
<li>Device Master Records (DMR)</li>
<li>Engineering Change Notices</li>
<li>New product development</li>
<li>Evaluate design feasibility of new product ideas and use design control processes to develop new product designs from concept to commercialization. </li>
<li>Develop product line extensions, changes, upgrades, and rework</li>
<li>Maintain existing product segments in accordance with company and industry standards.</li>
<li>Design Verification and validation activities</li>
<li>Testing protocols, data collection, data analysis, and technical report preparation.</li>
<li>Manage transfer to manufacturing, including vendor support. </li>
<li>Provide support to Clinical and Regulatory Affairs for submissions and responses to FDA.</li>
<li>Other duties specifically assigned by management.</li>
</ul>
 
Requirements:
This position requires the following qualifications (at a minimum):
<ul>
<li>Engineering degree – Bachelor’s (BS) or Master’s (MS) Degree in Mechanical, Biomedical, or Biomechanical preferred.</li>
</ul>
Experience
<ul>
<li>5+ years minimum experience in engineering or engineering related role. </li>
<li>Product Design - Experience leading or supporting engineering design projects in a fast-paced environment.</li>
<li>Computer Aided Design – Proficiency in SolidWorks, Pro/Engineer (Creo) preferred. Other computer aided design software packages will be considered.</li>
<li>Experience building 3D CAD parts, assemblies, manufacturing drawings, and bill of materials</li>
<li>Experience implementing Geometric Dimensioning and Tolerancing (GD&amp;T) per ASME Y14.5.</li>
<li>Experience processing Engineering Change Orders (ECO, ECN, ECR, or CRN’s)</li>
<li>Experience with standard industry or medical device regulated quality management system (ISO 9001, ISO 13485, 21 CFR 820).</li>
<li>Strong analytical and problem-solving skills.</li>
<li>Strong organizational skills.</li>
<li>Strong MS Office skills (Excel, Word, PowerPoint, Outlook).</li>
</ul>
Preferred Experience
<ul>
<li>2+ years direct engineering experience class I/II orthopedic instruments and medical device implants. </li>
<li>Experience working in manufacturing and quality inspection environment.</li>
<li>Product Data Management (PDM) – Experience with SolidWorks PDM.</li>
<li>Material Requirements Planning (MRP) - Experience with Syspro or equivalent MRP software.</li>
<li>Prior experience working in the medical device or orthopedics industry.</li>
</ul>
We offer company holidays, vacation and sick time off, medical, dental, vision, disability and life benefits as well as a 401(k) Plan. 
Shalby Advanced Technologies, Inc. provides equal employment opportunities to applicants and employees without regard to: age, genetic information/characteristics, marital status, medical condition, mental or physical disability, national origin and ancestry, pregnancy and perceived pregnancy, race and color, religion, sex/gender including pregnancy, breastfeeding, gender identity or gender expression, sexual stereotypes, sexual orientation, reproductive health decision-making and veteran or military status.
The expected base salary range for this position is between $85,000 to $105,000 annually and the compensation offered will depend on the candidate’s qualifications.

581 biomedical engineer Jobs