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field_job_occupational_field_parents_all

job_organization_name

city

state

<h3>Job Description</h3>
Job Description
Position Summary:&nbsp;
The anticipated annual base pay range for this full-time position is $65,000-$125,000.&nbsp;Actual base pay will be determined based on various factors, including years of relevant experience, training, qualifications, and internal equity. The compensation package may also include an annual bonus target, subject to eligibility and other requirements. Additionally, we offer a comprehensive benefits package to employees, including a 401(k) plan with employer match, 12 weeks of paid parental leave, health plans (medical, dental, and vision), life insurance and disability, and generous paid time off.
At TÜV SÜD America, we are passionate about technology, people, and the environment. For over 150 years, our employee’s contributions and enthusiasm have been essential to the success of our business. Our commitment is to invest in our employees as well as to hire, develop, and engage the best talent to help us continue to build our team. We are dedicated to creating a work environment where all levels of employees are inspired to learn, grow, and be empowered to achieve both their professional as well as personal goals.
We are seeking a highly skilled and experienced Senior Product Safety Engineer to join our Product Service division in San Diego, CA. This position will play a crucial role in ensuring the safety and compliance of various products through rigorous testing and evaluation.
This position is an onsite, fulltime, exempt position in San Diego, CA.
Responsibilities:
- Act as a Senior Safety Engineer, conducting inspections, tests, and conformity assessments of products using international and national regulations.
- Prepare and deliver Certificates, Test Reports, and Technical Reports to clients.
- Develop and execute test plans, analyze client input, and determine testing requirements.
- Operate standard test equipment, including oscilloscopes, multi-meters, dielectric strength testers, and environmental condition chambers.
- Perform comprehensive construction reviews and document findings in accordance with relevant Product Safety Standards (60950-1, 60950-22, 60529, 62368-1, 61010 series, 60335-1 series, 60825-1)
- Maintain accurate and timely test documentation and ensure proper calibration and functioning of all test equipment.
- Communicate effectively with internal and external customers, providing quotes, technical feedback and information regarding standards and test procedures and technical recommendations to achieve compliance and certification.
- Ensure the confidentiality of customers, tested products, and relevant internal information is maintained
- Stay up-to-date with the latest design theories, product standards, test procedures, and technology through continuous learning and training.
- Participate in customer kick-off meetings and audits (internal/external) as part of the regional product safety team.
- Mentor and provide guidance to junior engineers and team members, fostering a collaborative and supportive work environment.
- Travel as needed to conduct or witness tests at client sites.
Qualification
Education and Experience:
- University Degree in Electrical / Biomedical Engineering / Mechanical / Engineering Technology, or a related field from an ABET accredited program.
- Minimum of 5 years of experience in product safety engineering or a related field.
- In-depth knowledge of IEC and UL standards, OSHA’s NRTL Program, and the IECEE’s CB Scheme.
Preferred:&nbsp;
- Experience with medical product safety standards.
- Previous experience in a leadership or senior engineering role.
Knowledge, Skills, and Abilities:
- Excellent analytical and problem-solving skills.
- Strong technical writing skills for preparing detailed technical reports.
- Excellent communication skills and the ability to work collaboratively with diverse teams.
- Proven ability to manage multiple projects and meet deadlines.
- Willingness to travel as required.
Additional information
Equal Opportunity Employer – Disability and Veteran
TÜV SÜD America, Inc. is an equal opportunity, affirmative action employer and considers qualified applicants for employment without regard to race, color, creed, religion, ancestry, marital status, genetics, national origin, sex, sexual orientation, gender identity and expression, age, physical or mental disability, veteran status and those laws, directives, and regulations of Federal, State, and Local governing bodies or agencies. We participate in the E-Verify Employment Verification Program.
For more information on applicable equal employment regulations, please refer to the following:&nbsp;Labor Law 2025
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NBp5o1tlHq

Product Safety Engineer

<h3>Job Description</h3>
Job DescriptionDescriptionProvide design, engineering, and analysis support to other engineers and designers in the development and maintenance of orthopedic implants and instruments. Key Responsibilities
<ul>
<li>Provide design, engineering, and analysis support to other engineers and designers in the development and maintenance of orthopedic implants and instruments.</li>
<li>Apply sound engineering problem-solving techniques to product development and maintenance tasks including design, analysis, material selection, inspection requirements and manufacturing process requirements.</li>
<li>Prepare and submit written and oral communications that describe product design concepts, attributes and performance and project status. Areas of involvement include regulatory submissions, design history files, device evaluation and testing, manufacturing or supplier support, quality control, packaging, operating room support, device complaint evaluation, patent disclosures and instrument refurbishment.</li>
<li>Define and execute product testing and validation protocols.</li>
<li>Establish appropriate project plan (i.e. define tasks, dependencies, schedule and resource requirements).</li>
<li>Complete and approve all Design History File documentation for assigned projects as required.</li>
<li>Lead a cross-functional project team (including both internal and external team members such as orthopedic surgeons) of one or several minor development projects. A minor project involves the modification, adaptation or extension of an existing product or product line.</li>
<li>Study and recommend improvements to existing products and processes. This entails staying “up to date” on emerging material and medical product technologies. This may be accomplished by attending seminars, classes and industry meetings. Contribute to the timely and accurate completion of the projects and tasks assigned to his/her team.</li>
<li>Know and apply the Quality System and any appropriate Federal and International standards.</li>
<li>Assist and support other employees, teams, and sales personnel as necessary.&nbsp;</li>
</ul>
 Skills Knowledge and ExpertiseEducation:
<ul>
<li>Bachelor’s Degree in Mechanical Engineering, Biomedical Engineering or equivalent from an accredited institution required.</li>
</ul>
&nbsp;Experience:
<ul>
<li>Must have a basic understanding of theoretical technical principles in the following areas: mechanical drafting, geometrical dimensioning and tolerancing, computer aided design, engineering statics and dynamics, mechanics of materials, mechanical engineering design, materials, and technical writing.&nbsp;</li>
</ul>
Functional/Technical Knowledge, Skills and Abilities Required:
<ul>
<li>Must have excellent communication (verbal &amp; written) and organizational skills.</li>
<li>Must have excellent interpersonal skills and must be able to work effectively in a team environment.</li>
<li>Must be creative and have the ability to independently apply theoretical technical principles to product design.</li>
<li>Must have the ability to apply parametric solid modeling and drafting conventions to design projects.</li>
<li>Must have knowledge of various software packages including Microsoft Office applications and CAD applications.</li>
<li>To fully meet team responsibilities, the individual will develop additional knowledge and skills in anatomy and physiology, especially as related to the musculo-skeletal system, fundamentals of orthopedic surgery (major joints), mechanical test methods and procedures, quality and inspection methods, manufacturing processes and methods, FDA/ISO requirements, project management, orthopedic implants and the materials used in orthopedic implants and instruments.&nbsp;</li>
<li>Travel 5-10%&nbsp;</li>
</ul>

Product Design Engineer

<h3>Job Description</h3>
Job Description
Are you an innovative Field Service Engineer with a passion for cutting-edge technology? Join Sightpath Medical, the premier provider of mobile cataract and LASIK services in the U.S. You’ll have the unique opportunity to work with advanced ophthalmic equipment while supporting top surgeons in a fast-paced and rewarding environment. Whether you’re an entry-level candidate or bring years of experience, we offer knowledge, collaboration, and a shared commitment to excellence.
 
Why Sightpath Medical?
<ul>
<li>Comprehensive Training: Gain hands-on experience with the latest in ophthalmic laser technology. We provide all the training you need to excel in the field.</li>
<li>Independent Work Environment: You’ll have the autonomy to manage your work effectively while being part of an expert team.</li>
<li>Travel: You will have ownership of an assigned territory you will manage with a company provided vehicle and equipment. Every day is different. You will move from facility to facility providing expert service to our customers.</li>
<li>Work-life balance: With 8-10 case days per month, enjoy flexibility on non-case days when working from home or while traveling.</li>
<li>Medical benefits including health, dental, vision, short/long-term disability, and health savings account.</li>
<li>401(k) plan with employer contribution.</li>
<li>Health and Wellness Program to support your well-being.</li>
</ul>
 
What You’ll Do:
<ul>
<li>Technical Expertise: Install, de-install, calibrate, and operate transportable lasers and related equipment at customer sites.</li>
<li>Surgical Support: Ensure all equipment is programmed and calibrated to surgeon specifications prior to surgeries. You will also support the Surgeons during surgery to ensure customer satisfaction.</li>
<li>Preventative Maintenance: Perform routine maintenance and repairs to maximize equipment performance and minimize downtime.</li>
<li>Troubleshooting: Diagnose and resolve equipment issues efficiently, ensuring seamless surgical procedures.</li>
<li>Sterile Technique and Clinical: Adhere to sterile techniques during surgeries to ensure patient safety. Comprehensive training will be provided for all clinical aspects and requirements.</li>
<li>Manual Labor: Willing and able to assist with equipment setup and transport.</li>
<li>Other Duties: Flexibility to take on additional responsibilities as required.</li>
</ul>
 
Who We’re Looking For:
<ul>
<li>Technical Degree: Degree in Laser Electro-optics, Biomedical Equipment Technology, Electronics, or a similar field; military training in related fields is also acceptable.</li>
<li>Hands-On Experience: Proficiency with basic electronics and test equipment. Experience with laser systems is a plus.</li>
<li>Adaptable and Travel-Ready: Comfortable with driving to various locations in assigned territory and staying overnight when needed. All travel expenses are covered (hotel stays, gas for company vehicle, and meal allowances while traveling).</li>
<li>Driving Record: Able to produce a valid driver's license and pass a Motor Vehicle Report (MVR)/ driving record.</li>
<li>Excellent Communicator: Able to build strong relationships quickly with surgeons and their teams.</li>
<li>Self-assured: Able to thrive in high-pressure environments with confidence and professionalism.</li>
<li>Organized and Detail-Oriented: Skilled at managing equipment and completing administrative tasks required to support assigned territory.</li>
<li>Physical Demands: Ability to lift up to 100 lbs. and stand for extended periods.</li>
</ul>
 
Relocation Assistance:
We offer relocation allowances for qualified candidates who may need to move to join our team.&nbsp;
 
Compensation Range:
<ul>
<li>$65,000 - $80,000 annually with bonus eligibility</li>
<li>Company credit card provided for company use including: hotel stays, gas for company vehicle, maintenance for vehicle, meal allowance (when an overnight stay is required for coverage purposes), etc.</li>
</ul>
SIGHTPATH is an equal opportunity employer. In accordance with applicable law, we prohibit discrimination based on race, color, religion, creed, gender, pregnancy or related medical conditions, age (40 and over), national origin or ancestry, physical or mental disability, genetic information or any other consideration protected by federal, state or local laws. Our commitment to equal opportunity employment applies to all persons involved in our operations and prohibits unlawful discrimination by any employee, including supervisors and coworkers.
 
PM25
 
Compensation details: 60000-75000 Yearly Salary
 
PId8790c562bd6-25405-38196172

Laser Engineer III

<h3>Job Description</h3>
Job Description
Company Overview: Second Order Effects (SOE) is an engineering consulting firm that transforms uncertainty into fully functional hardware and software. We work on projects at all stages of development; we perform analysis, build prototypes, and take products to market. Our team solves high-impact problems across numerous industries, including automotive, aerospace, consumer electronics, industrial automation, biomedical, and green energy. Our designs control rocket engines, manage satellite communications, instrument fusion reactors, and are enjoyed by consumers around the world. The only thing we won't build is weapons.
Founded in 2016, Second Order Effects has 50+ employees (and counting!) in offices in El Segundo, California and Redmond, Washington. We've worked with &gt;130 clients on &gt; 300 projects as a partner, on retainer, or on demand.
How do we do this? We empower others, build the right thing, lead with curiosity, and own the outcome. Learn more at soeffects.com!
Team Overview: Mechanical engineering at SOE is a growth discipline but still rooted in the pioneering spirit that has driven us from the start. From our early innovations like RF combiners featuring custom copper-tungsten elements and phased-array speakers in acoustically-optimized enclosures, the close coupling between electrical and mechanical design persists as a cornerstone of our company. As our projects become more ambitious and complex, our mechanical engineering team continues to rise to the challenge.
Being part of the mechanical engineering team is an opportunity to contribute to a dynamic, growth focused environment, where we thrive on collaboration, interdisciplinary learning, continuous personal and professional development. We take ownership of our work and support one another through that growth. We look forward to welcoming you to the team!
Job Overview: As a Senior Mechanical Engineer, you will be part of a core SOE team and support all of the projects by designing enclosures, mechanisms, and custom parts for customers. Ideally, you are forward thinking and have solid experience carrying projects from whiteboard design through fabrication and test. Additionally, you must effectively communicate technical concepts to all audiences and balance creativity and technical foundations, as innovation requires both. What You Will Do: 
<ul>
<li>Own the technical direction of mechanical projects, aligning different engineering disciplines (Electrical, Embedded, Integration &amp; Test, etc.) and customers towards shared solutions </li>
<li>Guide the design, development, prototyping, and testing of mechanical systems and components, ensuring they meet all performance, quality, and safety standards</li>
<li>Provide hands-on guidance to the engineering team, offering technical support, mentorship, strategic planning, resource management</li>
<li>Perform complex mechanical assessments (Structural, Thermal, and Fluid Dynamics), design and model complex integrated 3D assemblies, and produce robust engineering drawings</li>
<li>Partner with Business Development (BD) to identify new opportunities and scope new business</li>
</ul>
We aim to provide a profile of someone who would thrive in this role. Even if this doesn't perfectly match your background, we encourage you to apply! SOE values diverse experiences and non-traditional career paths.
What You Will Need:
<ul>
<li>Bachelor's Degree in Mechanical Engineering, Physics, Math, or a related field</li>
<li>7+ years of experience in mechatronics engineering, including design, analysis, and project management</li>
<li>Expertise in electro-mechanical systems, including kinematics, dynamics, sensors, actuators, controllers, motor-driven mechanisms, and robotics</li>
<li>Strong design and spatial reasoning skills, proficiency in CAD software, GD&amp;T frameworks, and exposure across multiple manufacturing processes such as machining, injection molding, and 3D printing</li>
<li>Ability to analyze and characterize electro-mechanical systems using classical and computational methods</li>
<li>Hands-on experience with microcontrollers, PLC programming, and integrating instruments (IMUs, encoders, power systems, etc.) for control and automation</li>
<li>Proven ability to manage projects, lead teams, and collaborate cross-functionally with mechanical, test, and electrical engineers</li>
<li>Strong problem-solving, communication, and leadership skills to drive technical execution, optimize designs, and deliver robust, scalable solutions in a fast-paced environment</li>
</ul>
What Would Be Useful:
<ul>
<li>Proven ability to lead team-based design and project management, working across disciplines to drive technical execution.</li>
<li>Experience with firmware/embedded aspects of robotic systems, including motor controllers, ROS, and signal integration (GPIO, serial, analog, digital)</li>
<li>Strong analytical skills in back-of-the-envelope calculations, FEA, and CAD modeling for design validation</li>
<li>Ability to assess and estimate structural loading from environmental factors</li>
<li>Experience with structural and thermal testing of electro-mechanical assemblies</li>
<li>Proficiency in cabling, wiring, power, communications, and monitoring components for complex system integration</li>
</ul>
Benefits:
<ul>
<li>Compensation range of $151,100-$183,400 + equity incentive plan</li>
<li>Flexible work hours and work from home policy </li>
<li>100% employer-paid health insurance (Medical, Dental, Vision) for employees + 50% dependent coverage</li>
<li>Unlimited paid time off policy, 11x paid company holidays, 12x paid sick days</li>
<li>401(k) retirement account and employer matching (Safe Harbor 4%)</li>
<li>Generous paid parental leave</li>
<li>Relocation assistance available if 50+ miles away from the office</li>
<li>Electric Vehicle (EV) charging ports</li>
<li>Daily catered lunches, snacks, and accessible kitchen</li>
</ul>
Additional Requirements: 
<ul>
<li>Applicant must be willing to work 40 hours a week on-site in El Segundo, California, USA</li>
<li>Applicant must be eligible to work on export controlled projects</li>
<li>Job Type: Full-time (Salary)</li>
</ul>
Export Control Requirements:
<ul>
<li>To conform with U.S. Government export control regulations, including the Export Administration Regulations (EAR), you must be a U.S. citizen, lawful permanent resident of the U.S., protected individual as defined by 8 U.S.C. 1324b(a)(3), or eligible to obtain the required authorizations from the U.S. Department of State. Unfortunately, we are unable to provide sponsorship at this time.</li>
</ul>
If you don't meet 100% of the preferred skills and experience, we encourage you to still apply! Second Order Effects is proud to be an Equal Opportunity Employer; employment with SOE is governed on the basis of excellence and will not be influenced in any manner by race, color, religion, gender, national origin/ethnicity, veteran status, disability status, age, sexual orientation, gender identity, marital status, mental or physical disability, or any other legally protected status.

Senior Mechanical Engineer

<h3>Job Description</h3>
Job Description
Quality Engineer 1
Contract though end of 2025
Pay $45 an hour
We are looking for a Quality Engineer 1 to join our team. In this role, you'll be responsible for developing and maintaining quality processes and inspection methods, including gauging, programming, and documentation. You will work closely with Quality Control, Product Development, and Manufacturing Operations to support daily production and site initiatives. A key part of your role will be ensuring our quality system remains compliant with both internal and external medical device industry standards and regulations.
We need a proactive individual who is eager to learn, has a solid understanding of manufacturing and quality principles, and possesses great communication skills. You should also be technically proficient with common software like Word and Excel and have a keen eye for detail. Experience with statistical analysis, software development, and familiarity with Tulip, Jira, and Agile methodology is highly preferred.
Competencies
<ul>
<li>Communication: Must be able to communicate effectively, both verbally and in writing.</li>
<li>Project Management: Effective project and time management skills; able to work independently and within a cross-functional team.</li>
<li>Technical Skills: Proficiency with PC applications, including Microsoft Word, Minitab, PowerPoint, MS Project, Visio, and Excel.</li>
<li>Collaboration: Frequent interaction with peers, management, production associates, and external suppliers.</li>
</ul>
salary: $44 - $45 per hour shift: First work hours: 8 AM - 9 PM education: Associate 
Responsibilities
Key Responsibilities
<ul>
<li>Design and Development: Create and implement various inspection techniques and procedures to ensure product integrity.</li>
<li>Documentation and Procedures: Write, approve, and implement inspection procedures for all stages of production (Receiving, Floor, Final) and support operator self-inspection.</li>
<li>Gauging and Tools: Work with other Quality Engineers and Metrology Lab personnel to develop and procure product gauging, optical comparator overlays, and templates.</li>
<li>Process Improvement: Coordinate and execute the development of quality processes, including work instructions, procedures, and test methods.</li>
<li>Training: Train Manufacturing Associates on measuring, testing, and inspection techniques.</li>
<li>Analysis and Validation: Perform first article inspections, capability studies, process validations, and metallurgical analyses as needed.</li>
<li>Problem Resolution: Collaborate with suppliers, engineers, and manufacturing associates to resolve quality issues by compiling and analyzing data, and presenting feedback to internal and external vendors.</li>
</ul>
Requirements
<ul>
<li>Education: Bachelor’s degree in Biomedical, Mechanical, Electrical, or a related Engineering or Technical discipline.</li>
<li>Experience: 0–2 years of experience in a technical or manufacturing role is preferred.</li>
<li>Certifications: ASQ CQE or Six Sigma Green Belt certification is a plus.</li>
</ul>
 Skills
<ul>
<li>Quality Assurance</li>
<li>Quality Control</li>
<li>Product Inspection</li>
<li>Monitoring</li>
 Qualifications
<li>Years of experience: 4 years</li>
<li>Experience level: Experienced</li>
 Randstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad. 
 Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact <a href="mailto:HRsupport@randstadusa.com" target="_blank">HRsupport@randstadusa.com</a>. Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&amp;D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility). This posting is open for thirty (30) days. 
</ul>

Quality Engineer 1

<h3>Job Description</h3>
Job DescriptionOur client, a world leader in Pharmaceuticals and In-Vitro Diagnostics (IVD) tools, is seeking a “Process Development Engineer” in Santa Clara, CA Duration: Longterm Contract with possible Full Time Conversion Description 
The Process Development Engineer provides technical and operational support for consumable and cartridge manufacturing, bridging new product implementation with process optimization to ensure compliance, quality, and manufacturing robustness. Responsibilities include process troubleshooting, validation (IQ/OQ/PQ), process characterization, in-process controls (CTQs/IPCs), root cause investigations, statistical analysis (DOE/SPC), and continuous improvement initiatives using Lean Six Sigma. The role requires strong collaboration in a GMP/ISO 13485 regulated environment, authorship of technical documentation (ERP/SAP), and participation in audits, CAPAs, and technology transfer from R&amp;D to operations. 
Qualifications: 
<ul>
<li>
Bachelor’s or higher in Biomedical, Chemical, Mechanical Engineering, or related discipline 
</li>
<li>
Minimum 5 years’ experience in medical device, IVD, or regulated manufacturing 
</li>
<li>
Hands-on experience with process validation, technology transfer, and manufacturing support 
</li>
<li>
Proficiency in DOE, SPC, and statistical tools (JMP, Minitab) 
</li>
<li>
Familiarity with GMP, ISO 13485, FDA QSR (21 CFR 820) compliance 
</li>
<li>
Experience with microfluidics, surface chemistry, reagent formulation, cleanroom operations, or automated liquid handling (preferred) 
</li>
<li>
Lean Six Sigma Green Belt certification (preferred) 
</li>
</ul>
 Please respond with your updated resume and contact information to <a href="mailto:hr@dawarconsulting.com" target="_blank">hr@dawarconsulting.com</a>/<a href="mailto:kavitha@dawarconsulting.com" target="_blank">kavitha@dawarconsulting.com</a>

Process Development Engineer

<h3>Job Description</h3>
Job Description
Join a leading healthcare technology service provider as an Imaging Engineer supporting a critical client site in the Wauseon, OH area. This is a full-day, on-site position with the flexibility of starting your day from home before heading to the client location. Ideal for professionals passionate about maintaining and servicing diagnostic imaging equipment in a high-impact healthcare setting.
APPY NOW!!
Key Responsibilities:
<ul>
<li>
Troubleshoot, calibrate, and repair a wide range of imaging equipment including X-ray, CT, MRI, ultrasound, and mammography systems.
</li>
<li>
Perform preventive maintenance and electrical safety checks on imaging and biomedical devices.
</li>
<li>
Provide technical support and guidance to clinical staff on equipment use and best practices.
</li>
<li>
Ensure all documentation, compliance standards, and customer service benchmarks are consistently met.
</li>
</ul>
Qualifications:
<ul>
<li>
Hands-on experience with general radiography, fluoroscopy, portable units, X-Ray, CT, MRI and C-Arms is required.
</li>
<li>
Associate degree in Biomedical Technology or a related technical field preferred.
</li>
<li>
CBET certification a plus.
</li>
<li>
Strong communication, problem-solving, and customer service skills essential for success in a hospital environment.
</li>
</ul>
Location: Remote Field Role – Report daily to a client site in Wauseon, OH Schedule: Full-time, Day Shift M-F Hourly Rate: $40.86 - $63.99/hr (Depending on Experience) Benefits: Comprehensive benefits package available
APPLY NOW!!
 Pay Details: $40.86 to $63.99 per hour Search managed by: Deanna Murphy 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.lhh.com/us/en/candidate-privacy" target="_blank">https://www.lhh.com/us/en/candidate-privacy</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>

Imaging Engineer

<h3>Job Description</h3>
Job DescriptionCareers With Purpose Sanford Health is one of the largest and fastest-growing not-for-profit health systems in the United States. We're proud to offer many development and advancement opportunities to our nearly 50,000 members of the Sanford Family who are dedicated to the work of health and healing across our broad footprint. Facility: Sanford Med Ctr Fargo Location: Fargo, ND Address: 5225 23rd Ave S, Fargo, ND 58104, USA Shift: Day Job Schedule: Full time Weekly Hours: 40.00 Salary Range: $34.50 - $57.00 Job Summary Provides advanced technical support to physicians, advanced practice providers, and clinical staff on clinical technologies. Provides expert planning for clinical technology expansion. The Lead Clinical Engineer is a key member of the perioperative services team, responsible for the oversight, integration, and optimization of advanced clinical technologies within the procedural environment. This role ensures the safe, effective, and efficient operation of complex systems including surgical navigation, robotic-assisted surgery platforms, integrated operating room systems, and patient monitoring technologies. The engineer serves as the primary technical expert and liaison between clinical staff, biomedical engineering, IT, and external service providers, ensuring that all perioperative technologies support optimal patient outcomes and clinical workflows. This position requires a deep understanding of electromechanical systems, software interfaces, and networked medical devices. The Lead Clinical Engineer will lead efforts in technology planning, acquisition, and implementation, contributing to capital equipment decisions and long-term strategic planning. They will be responsible for troubleshooting and resolving technical issues in real-time, including during surgical procedures, and will conduct root cause analyses for adverse events involving clinical technologies. The role also includes supporting preventive maintenance schedules, performing minor repairs, and coordinating emergency service responses when necessary. In addition to technical responsibilities, the Lead Clinical Engineer will develop and deliver training programs for clinical staff, ensuring safe and proficient use of surgical technologies. They will also play a critical role in policy development, compliance with regulatory standards, and continuous quality improvement initiatives. The ideal candidate will possess strong leadership, communication, and problem-solving skills, and will thrive in a fast-paced, high-stakes environment where collaboration and adaptability are essential. This role is embedded within the surgical services department and may require direct support during patient care activities. The Lead Clinical Engineer is expected to be a proactive innovator, continuously seeking opportunities to enhance the integration and performance of clinical technologies in support of surgical excellence. Qualifications Bachelor’s degree required or Master’s degree preferred in mechanical engineering, biomedical engineering, industrial engineering or a similar engineering or scientific background. Two years’ experience working with medical equipment, and background in equipment testing and quality control/quality assurance preferred. Professional Engineer (PE) license preferred. If PE license is not obtained, background experience or Master’s degree is highly preferred. Benefits Sanford Health offers an attractive benefits package for qualifying full-time and part-time employees. Depending on eligibility, a variety of benefits include health insurance, dental insurance, vision insurance, life insurance, a 401(k) retirement plan, work/life balance benefits, and a generous time off package to maintain a healthy home-work balance. For more information about Total Rewards, visit <a href="https://sanfordcareers.com/benefits" target="_blank">https://sanfordcareers.com/benefits</a> . Sanford is an EEO/AA Employer M/F/Disability/Vet. If you are an individual with a disability and would like to request an accommodation for help with your online application, please call 1-877-673-0854 or send an email to <a href="mailto:talent@sanfordhealth.org" target="_blank">talent@sanfordhealth.org</a> . Sanford Health has a Drug Free Workplace Policy. An accepted offer will require a drug screen and pre-employment background screening as a condition of employment. Req Number: R-0236058 Job Function: Allied Health Featured: No

Lead Clinical Engineer - Surgical Services

<h3>Job Description</h3>
Job DescriptionJob Summary
We are seeking a hands-on Quality Engineer to join our team. This role is crucial for ensuring the highest quality, safety, and effectiveness of our medical devices. You will be instrumental in both executing key quality tasks and supporting the continuous development and adherence to our Quality Management System (QMS). This is an exciting opportunity to directly impact product quality and regulatory compliance in a growing, innovative company.
Responsibilities
<ul>
<li>Contribute to the development, implementation, and maintenance of our Quality Management System (QMS) and associated standards.</li>
<li>Plan and execute incoming inspections for components and materials.</li>
<li>Support and optimize production line testing of our devices to ensure consistent quality.</li>
<li>Actively support design and development activities, including design reviews, verification, validation, and maintaining the Design History File (DHF) for both new and existing products.</li>
<li>Participate in risk analysis and management activities in accordance with ISO 14971, ensuring product safety throughout the lifecycle.</li>
<li>Investigate product complaints, reported quality issues, and nonconformities.</li>
<li>Drive root cause analysis and implement effective corrective and preventive action plans (CAPAs) to prevent recurrence.</li>
<li>Support supplier qualification, monitoring, and corrective actions to ensure the quality of supplied components and services.</li>
<li>Develop, review, and approve essential QMS documentation, including SOPs, work instructions, test plans, protocols, and reports.</li>
<li>Ensure strict adherence to medical device regulations such as FDA 21 CFR Part 820, ISO 13485, IEC 60601-1, IEC 62304. Provide quality support for regulatory submissions, including 510(k) activities.</li>
<li>Prepare and maintain documentation to ensure audit readiness and support internal and external audits.</li>
<li>Identify and implement opportunities for process improvement within the QMS and across the product development and manufacturing lifecycles.</li>
<li>Work closely with R&amp;D, Engineering, Manufacturing, and Regulatory Affairs teams, serving as a hands-on quality resource to integrate quality requirements effectively.</li>
</ul>
Qualifications
<ul>
<li>Bachelor's degree in Biomedical Engineering, Electrical Engineering, Mechanical Engineering, or a related scientific discipline.</li>
<li>5+ years of direct experience as a Quality Engineer in the medical device industry.</li>
<li>Proven hands-on experience in developing and implementing quality systems and standards.</li>
<li>Solid understanding and practical experience with medical device regulations and standards, including FDA 21 CFR Part 820, ISO 13485, IEC 60601-1, IEC 62304, and IEC 60601-2-37.</li>
<li>Demonstrated experience in planning and executing incoming inspections and production line testing of products/components.</li>
<li>Experience investigating product complaints, quality issues, and nonconformities.</li>
<li>Track record of developing and implementing corrective and preventive action plans (CAPAs).</li>
<li>Familiarity with Design Controls, Risk Management (ISO 14971), and supporting regulatory submissions (e.g., 510(k)).</li>
<li>Experience with electronic Quality Management Systems.</li>
<li>Strong analytical, problem-solving, and critical thinking skills.</li>
<li>Excellent communication skills, both written and verbal, for effective documentation and cross-functional collaboration.</li>
<li>Highly detail-oriented with the ability to manage multiple tasks in a dynamic, fast-paced startup environment.</li>
</ul>
Preferred Qualifications:
<ul>
<li>Experience with ultrasound devices.</li>
<li>Experience with Enzyme eQMS</li>
<li>ASQ Certified Quality Engineer (CQE) or other relevant quality certifications.</li>
<li>Direct experience supporting a medical device product through initial manufacturing scale-up and commercial launch.</li>
</ul>
 Job Posted by ApplicantPro

Quality Engineer

<h3>Job Description</h3>
Job DescriptionSalary: $72,000-$93,000 
Injectech, LLC has been a trusted supplier of fluid-control components for over 20 years. Our current senior management team has been with Injectech since the very beginning, bringing extensive knowledge of the medical device industry to every project.
 
Our Employees are important to us! We want the best for our employees, not just at work, but through all aspects of their life. That is why we pay 100% of the employees share of health insurance cost and match up to 6% for our 401k plan and provide free financial advice about retirement, debt, and any future financial needs from a licensed Financial Advisor. We strongly believe that the only way for our company to be successful is to make sure our employees have healthcare, mental healthcare, retirement options and financial education available to them.
 
We work hard to create a culture that promotes open lines of communication, a flexible work-life balance, continuous improvement in every department, and a place where employees want to be every day. We strive to hire and retain the best people, because we know a company is only as good as its employees. We hope you will join our team as we continue to grow and improve! 
Job Summary:
We are seeking a highly skilled and detail-oriented Medical Injection Molding Process Engineer to lead the development, optimization, and validation of injection molding processes used to manufacture precision medical components. This role is responsible for ensuring robust, repeatable, and compliant manufacturing processes that meet regulatory requirements (ISO 13485) and support high-volume production in a cleanroom environment. The Process Engineer will play a key role in new product introductions, continuous improvement initiatives, and troubleshooting activities.
 
General Duties (includes but not limited to):
<ul>
<li>Develop, optimize, and validate injection molding processes for new and existing medical products.</li>
<li>Lead mold and material trials, establish robust process windows, and conduct Design of Experiments (DOE) to optimize quality and efficiency.</li>
<li>Collaborate with R&amp;D, tooling, quality, and manufacturing teams during product development and commercialization.</li>
<li>Author and execute validation protocols (IQ, OQ, PQ) in compliance with ISO 13485 requirements.</li>
<li>Troubleshoot molding and tooling issues; implement root cause analysis and corrective actions (CAPA).</li>
<li>Evaluate and approve mold designs, materials, and process control plans to ensure manufacturability and scalability.</li>
<li>Specify and support installation of new injection molding machines, robotics, and auxiliary equipment.</li>
<li>Analyze process data using risk-based (e.g., PFMEA) and statistical methods (e.g., SPC, SixmaXL); maintain documentation of process settings and changes.</li>
<li>Drive continuous improvement initiatives focused on yield, cycle time, scrap reduction, and cost savings.</li>
<li>Train technicians and operators on molding best practices, process control, and cleanroom requirements.</li>
<li>Ensure compliance with cleanroom protocols and current Good Manufacturing Practices (cGMP).</li>
</ul>
 
Qualifications:
Education &amp; Experience:
<ul>
<li>Bachelors degree in Plastics Engineering, Mechanical/Industrial Engineering, Biomedical Engineering, or related field.</li>
<li>37 years of experience in injection molding process development, with a focus on medical device manufacturing.</li>
<li>Experience in a regulated cleanroom environment (ISO Class 7/8) and with medical-grade and engineering materials (e.g., PC, PA, ABS, Acrylic, PP).</li>
</ul>
Skills &amp; Competencies:
<ul>
<li>Deep knowledge of injection molding principles, mold design, and thermoplastic materials.</li>
<li>Ability to learn and adhere to electronic Quality Management System (eQMS). </li>
<li>Proficient in scientific injection molding techniques and DOE methodology.</li>
<li>Familiarity with validation practices per ISO 13485 standards.</li>
<li>Experience with injection molding equipment (e.g., Fanuc, JSW) and related software (RJG, SigmaXL, etc.).</li>
<li>Strong analytical, troubleshooting, and project management skills.</li>
<li>Excellent written and verbal communication; ability to write technical reports and validation documentation.</li>
<li>Detail-oriented, quality-focused, and able to work independently or in cross-functional teams.</li>
</ul>
 
Working Conditions:
<ul>
<li>Work performed in both office and ISO Class 7/8 cleanroom manufacturing environments.</li>
<li>Occasional travel to suppliers or tooling vendors may be required.</li>
<li>Use of personal protective equipment (PPE) and adherence to cleanroom protocols is mandatory.</li>
</ul>
 
Benefits
<ul>
<li>401K Retirement Plan- Eligible to contribute starting the first of the month, 2 months after your hire date. Injectech matches up to 6% of your salary. Contributions are 100% invested immediately. Both Roth and Traditional options are available.</li>
<li>Health Insurance- Coverage begins the first of the month after 30 days of employment. Injectech covers 100% of the employees' premium. You may add a spouse, domestic partner, or dependents at your own cost via pre-tax payroll deductions. </li>
<li>Dental, Vision and Supplemental Insurance Plans- Offered at a group discount rate for employees, spouses, domestic partners, and dependents.</li>
<li>Employee Assistance Program- Available to all employees and their family members at no cost. </li>
</ul>
<ul>
<li>Sick Time- Accrues at 1 hour for every 30 hours worked, up to 48 hours per year.</li>
<li>Paid Time Off (PTO)
<ul>
<li>First 36 months: 6.66 hours per month (up to 80 hours per year).</li>
<li>After 36 months: 8 hours per month (up to 96 hours per year).</li>
<li>Accrual rates continue to increase with tenure.</li>
</ul>
</li>
<li>Holiday Pay- 10 paid holidays per year.</li>
<li>Voluntary Paid Time Off (VTO)- Up to 20 hours per year to volunteer at any 501(c)(3) nonprofit of your choice.</li>
<li>Life and AD&amp;D Insurance- Injectech provides a $50,000 policy at no cost to employees. Additional coverage is available for purchase.</li>
</ul>
Effective 6 Months After Hire Date:
<ul>
<li>Profit Share Program- Eligible to participate the month following 6 full months of employment.</li>
</ul>
 
Drug Testing Policy
Injectech is committed to maintaining a safe and productive workplace. As part of this commitment, all potential employees must pass a drug screening as a condition of employment. The drug test is a 5-panel screening and must be completed prior to your start date.
 
Injectech is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, disability, or any other characteristic protected by law. We are committed to creating a diverse and inclusive workplace and encourage candidates from all backgrounds to apply.

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