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job_organization_name

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<h3>Job Description</h3>
Job Description
A-Line Staffing is now hiring an On-Site Systems Engineer in San Diego, CA 92121. This role offers career growth potential and the opportunity to work with a Fortune 500 company. This is a full-time position, working 40+ hours per week.
If you are interested in this Systems Engineer position, please contact Heather Foret at <a href="mailto:Hforet@alinestaffing.com" target="_blank">Hforet@alinestaffing.com</a>.
Systems Engineer Compensation
<ul>
<li>The pay for this position is $69.44 per hour</li>
<li>Benefits are available to full-time employees after 90 days of employment</li>
<li>A 401(k) with a company match is available for full-time employees with 1 year of service on our eligibility dates</li>
</ul>
Systems Engineer Position Highlights
<ul>
<li>This is a contract assignment with potential for permanent hire based on attendance, performance, and business needs</li>
<li>The required availability for this position is Monday-Friday with Friday remote</li>
</ul>
Systems Engineer Responsibilities
<ul>
<li>Provide systems leadership through various phases of the product lifecycle</li>
<li>Translate voice of customer and stakeholder needs into system and product requirements</li>
<li>Conduct feasibility and risk assessments at the system/product level</li>
<li>Facilitate cross-functional knowledge sharing to resolve product development issues</li>
<li>Coordinate system-level product development and integration</li>
<li>Investigate and resolve system behavior issues for on-market products</li>
<li>Identify opportunities and drive continuous improvement initiatives</li>
<li>Apply DFSS (Design for Six Sigma) best practices in all projects</li>
</ul>
Systems Engineer
<ul>
<li>5+ years of system engineering experience – electrical or biomedical</li>
<li>Experience with Requirements Management in QMS</li>
<li>Experience generating requirements, including identifying input sources for requirements</li>
<li>Experience with traceability</li>
<li>Experience with Safety Standards: 60601-1 &amp; 60601-1-2, 14971, 15223, 2417</li>
</ul>
<ul>
<li>Bachelor’s degree in Science or Engineering (Postgraduate degree preferred)</li>
<li>At least 5 years of related work experience (combination of work experience and advanced degrees considered)</li>
<li>Strong background in Systems Engineering, medical device development, or a similar field</li>
<li>Experience in systems integration and testing, system architecture, Reliability Engineering, Project Management, and Failure Modes Effects Analysis</li>
<li>Familiarity with Systems Engineering and requirements management</li>
<li>Ability to lead multi-discipline engineering teams and work independently or collaboratively</li>
<li>Proficiency in DFSS, statistical test design and analysis, or Critical Parameter Management</li>
<li>Excellent communication and writing skills, with attention to detail</li>
<li>Experience working in an agile development environment is a plus</li>
</ul>
If you think this Systems Engineer position is a good fit for you, please reach out to me—feel free to call, email, or apply to this posting!

Systems Engineer

<h3>Job Description</h3>
Job Description
We are seeking a skilled temp-to-hire Process Engineer to join a dynamic biotech industry team. The Process Engineer will lead multiple aspects of manufacturing equipment and process design and validation. The Process Engineer will work closely with a cross functional team while maintaining equipment uptime and improving upon product cost, quality, and safety. 
Essential Duties and Responsibilities 
<ul>
<li>Responsible for developing manufacturing and assembly processes consistent with Design for Manufacturability for new product introductions. </li>
<li>Designs, executes and documents process validation protocols in support of quality and regulatory requirements. </li>
<li>Provides on-demand pilot line support, managing manufacturing metrics (yields, cycle times, capacity, bottlenecks), ensuring adherence to quality and compliance procedures, identifying and implementing continuous process improvements, deploying new fixture and tooling, and supporting manufacturing documentation updates. </li>
<li>Identifies and develops the crucial equipment related to new product development and maintains appropriate uptime for current equipment. </li>
<li>Assists pilot line technicians and engineers on manufacturing problems. Purchases and designs equipment that meets safety and environmental requirements. </li>
<li>Responsible for communicating business related issues or opportunities to next management level </li>
<li>Responsible for ensuring personnel and Company compliance with all Federal, State, local and Company regulations, policies, and procedures. </li>
<li>Lead or support troubleshooting activities and process improvements. Perform root cause analysis of failures. Work on special projects as requested by management. </li>
<li>Assist with other responsibilities and/or projects as the need arises. </li>
</ul>
 Requirements
<ul>
<li> Bachelor’s degree in Mechanical Engineering, Biomedical Engineering or related field is required </li>
<li>Minimum of 2 years of industry process engineer experience is required </li>
<li>Experience with commercial or pilot manufacturing lines, technical report writing, statistical analysis and data evaluation is required. </li>
<li>Knowledge of good manufacturing practices and documentation is required </li>
<li>Strong Project Management experience and skills are preferred. </li>
<li>The ability to influence others to achieve business objectives. </li>
<li>Excellent written and oral communication skills is required. </li>
<li>Knowledge of production processes, standard costs and work standards highly preferred </li>
<li>Ensure personal and company compliance with all Federal, State, local and Company regulations, policies, and procedures. </li>
<li>Experience in a regulated industry is required; medical device experience is a plus. </li>
<li>Ability to travel up to 10%, international and domestic, is required. </li>
</ul>
 
Desired skills and traits 
<ul>
<li>Attention to Detail </li>
<li>Communication (written and verbal) </li>
<li>Computer Proficiency </li>
<li>Leadership </li>
<li>Microsoft Suite (Excel, Word, Outlook, PP) </li>
<li>Seasoned experience in multiple facets of manufacturing operations </li>
<li>Experience in Lean/Six Sigma. </li>
<li>Hands-on leader who understands employee engagement, is a strong team builder, coach, and Understands the importance of culture and being true to the core values of the organization </li>
</ul>
 
 BenefitsCompany provided lunch to all employees when working at the work site.

Process Engineer

<h3>Job Description</h3>
Job Description
Our client, a leader in the manufacturing of devices and components for major medical device companies, is looking for a Principal Application Engineer to join their organization. 
They offer competitive compensation and excellent benefits, including 401k, health/dental, vision, and paid time off. They maintain a modern, clean, and safe facility with state-of-the-art equipment and dedication to continuous improvement. The company is registered with the FDA as a Class 2 and Class 3 Medical Device Manufacturer and is certified to ISO 13485. 
SUMMARY OF POSITION:
Reporting to the Sr. Engineering Manager, this position will have direct responsibility for key production-related deliverables including, but not limited to Manufacturing plan; Capacity planning; COGS estimation; Process validations; Capital equipment specifications and procurement; Production line set-up, as well as coordinate the launch of new products into production. The company manufactures parts via high precision metal machining, finishing, assembly, and anodize processes for Medical Devices. 
ESSENTIAL FUNCTIONS:
<ul>
<li>This position may have direct-reporting responsibilities for daily activities of site Engineering personnel (responsibility dependent on geographic organizational structure). </li>
</ul>
<ul>
<li>Develop and perform installation, operational and process qualifications for customer manufacturing processes in cooperation with cross-functional engineering teams per project requirements. </li>
</ul>
<ul>
<li>Ability to program various pieces of CNC equipment across multiple sites as directed to support critical and/or high-value projects milling, turning, and grinding, Multi spindle, Multi Axis and Swiss style programs for manufacture of medical devices- implants and instruments. </li>
</ul>
<ul>
<li>Analyze drawings, design models, and sketches to determine dimensions and configuration of cuts, selection of cutting tools, machine speeds, and feed rates according to shop processes, customer specifications, and machine capabilities. </li>
</ul>
<ul>
<li>Actively participate in process development projects and DFM with internal and external teams </li>
</ul>
<ul>
<li>Revise programs to eliminate instruction errors, omissions, and update programs with new technology/methods to improve efficiency; meet customer delivery dates </li>
</ul>
<ul>
<li>Coordinate with Quality Engineering to help facilitate the development of Process Control Plans, Manufacturing Inspection Plans, and gaging/fixturing requirements. </li>
</ul>
<ul>
<li>Create 1st pcs and in-process inspection plans. </li>
</ul>
<ul>
<li>Design fixtures for post processing operations. </li>
</ul>
<ul>
<li>Adapts machine or equipment design to facility and production conditions. </li>
</ul>
<ul>
<li>May incorporate inspection and test requirements into the production plan. </li>
</ul>
<ul>
<li>Inspects performance of machinery, equipment, and tools to verify their efficiency, and investigates and initiates corrective action of problems and deficiencies to ensure product quality. </li>
</ul>
<ul>
<li>Develops manufacturing processes that are applicable to statistical process control and may develop those techniques. </li>
</ul>
<ul>
<li>Provides guidance to engineering regarding design concepts and specification requirements to best utilize equipment and manufacturing techniques. </li>
</ul>
<ul>
<li>Identify and support business growth opportunities and present recommendations to management. </li>
</ul>
<ul>
<li>May be required to act as lead technical problem solver within area of specialization. </li>
</ul>
<ul>
<li>Develop and deliver presentations to communicate status, problem resolution or promote related business products. </li>
</ul>
QUALIFICATIONS:
<ul>
<li>Bachelor's degree (mechanical engineering, biomedical engineering, or related) required, with a related advanced degree preferred. </li>
</ul>
<ul>
<li>Minimum of 7 years' experience within a regulated industry (preferably in a Medical Device or Aerospace Manufacturer). </li>
</ul>
<ul>
<li>Project management experience - plan, development and execution. </li>
</ul>
<ul>
<li>Ability to read drawings and specifications containing GD&amp;T. </li>
</ul>
<ul>
<li>Familiarity with technologies and methods used to define how products are to be manufactured, how to conduct analysis, and meeting quality and compliance standards. </li>
</ul>
<ul>
<li>Extensive experience with transferring multi-disciplinary products from development to production. </li>
</ul>
<ul>
<li>Possess a high attention to detail. </li>
</ul>
<ul>
<li>Proficiency in SolidWorks </li>
</ul>
<ul>
<li>Proficient in the use of Microsoft Office, and Adobe products. </li>
</ul>
<ul>
<li>Experience associated with continuous improvement activities, including participations and/or facilitating Kaizen events using lean manufacturing principles. </li>
</ul>

Principal Application Engineer/CNC Programmer

<h3>Job Description</h3>
Job Description
CFD Research is seeking a mid-level research engineer to support the research and development of multiple simulation codes with a primary focus on supporting the CFD Research HEAT software package. The candidate will be part of a team focused on developing tools in support of hypersonic vehicle modeling including: TPS aerothermal response, boundary layer modeling, material ablation and decomposition, hypersonic external flow, Lagrangian particle tracking, mesh shape change and grid adaptation, and more. The candidate should have experience deriving and implementing numerical solvers for physics-based equations as well as code development experience in Fortran, C/C++, and Python.
Basic Qualifications:
<ul>
<li>
Candidate must be a US Citizen and meet eligibility to obtain (and maintain) a Secret Clearance
</li>
<li>
MS in Aerospace or Mechanical Engineering (or related STEM discipline) + at least two years relevant experience
</li>
<li>
Candidate must have experience in compiled languages such as Fortran and/or C/C++ and knowledge of code compilation and development on Linux.
</li>
<li>
Experience with Python programming
</li>
<li>
Additional technical skills as follows: Gitlab, CMake, OOP, Bash/Power Shell, compressible flows, numerical methods, linear algebra, hypersonics coursework
</li>
</ul>
Preferred Qualifications:
<ul>
<li>
Active secret level clearance
</li>
<li>
PhD preferred
</li>
<li>
Experience developing CFD codes, linear solvers, or algorithms of similar complexity
</li>
<li>
Additional preferred skills/experience: Fortran 2008+, Git, Docker, Valgrind, gprof (or Intel equivalents), and parallel computing / multi-threading.
</li>
</ul>
Location: This role is based in the Huntsville, AL area, and is 100% onsite.
About CFD Research: Since its inception in 1987, CFD Research has delivered innovative technology solutions within the Aerospace &amp; Defense, Biomedical &amp; Life Sciences, Intelligence &amp; Sensing, and Energy &amp; Materials industries. CFD Research has earned multiple national awards for successful application and commercialization of innovative component/system technology prototypes, multi-physics simulation software, multi-disciplinary analyses, and expert support services. Based in Huntsville, Alabama where laboratory facilities and headquarters are located, CFD Research also has office and laboratory facilities in Dayton, Ohio, prototyping test and evaluation facilities in Hollywood, Alabama, and office facilities in Fort Walton Beach, Florida. CFD Research is an ISO9001:AS9100D registered company and is appraised at CMMI Level II for Services. CFD Research is a 100% ESOP (employee-owned company) recognized in Inc. Magazine's Inc5000 as a top growing company for four of the last five years. Learn more at <a href="http://www.cfd-research.com" target="_blank">www.cfd-research.com</a>
 
Benefits: CFD Research offers competitive salaries and excellent employee benefits, including an employer matching 401(k) and Employee Stock Ownership Plan (ESOP). CFD Research offers a highly competitive insurance package, including medical, vision, and dental insurance. We offer company paid leave, compensation time, parental leave, long-term and short-term disability, accidental death and dismemberment, and life insurance. Performance appraisals occur twice a year and annual pay increases are based upon corporate goals, personal development, performance, and outstanding achievements. In addition, group and individual bonuses are awarded for exceptional performance.
CFD Research is an EO employer - Veterans/Disabled and other protected categories
 Job Posted by ApplicantPro

Senior Research Engineer (Computational Engineering / Development)

<h3>Job Description</h3>
Job Description Company Description:&nbsp; SynCardia Systems, LLC, a Picard Medical Company, is headquartered in Tucson, AZ. We manufacture and sell the world's first and only US Food and Drug Administration (FDA) and Health Canada approved total artificial heart as bridge to transplant for patients suffering from biventricular heart failure The SynCardia Total Artificial Heart™ is available in two sizes to accommodate patients’ diverse physiologies. The Freedom Portable Driver™ allows clinically stable patients to be discharged from the hospital to enjoy life at home while they wait for a heart transplant. The SynCardia Total Artificial Heart™ has been successfully used in over 2,000 patients and is the most widely used and extensively studied total artificial heart in the world. For additional information and label information, visit us at <a href="http://www.syncardia.com" target="_blank">www.syncardia.com</a>. Position Description:&nbsp; SynCardia Systems, LLC is seeking a Mechanical Engineer to support the production and manufacturing of our Total Artificial Heart System. This role focuses on sustaining engineering efforts, ensuring compliance with regulatory standards, and driving continuous process improvements. Responsibilities:&nbsp;
<ul>
<li>Provide mechanical engineering and project leadership to support existing Total Artificial Heart System productions in Sustaining Engineering and manufacturing as required by business needs.</li>
<li>Provide engineering information by answering questions and requests.</li>
<li>Maintain product and company reputation by complying with government regulations.</li>
<li>Maintain good documentation practices for all aspects of work.</li>
<li>Participate in related company projects to gain a solid working understanding of SynCardia business and quality systems.&nbsp;</li>
<li>Maintain professional and technical knowledge by attending educational workshops; reviewing professional publications; establishing personal networks; participating in professional societies.</li>
<li>Develop and manage budgets, timelines, and resources for manufacturing projects.</li>
<li>Train and mentor team members to promote professional growth and development.</li>
<li>Develop and execute plans to ramp up production capacity in response to increased demand or new product introductions</li>
<li>Manage the transfer of production processes and equipment from development to manufacturing, ensuring all requirements are met and risks are mitigated.</li>
<li>Develop and validate tooling designs which meet the requirements of the manufacturing process, including precision, repeatability, and ease of use.</li>
<li>Use value stream mapping to visualize and analyze the flow of materials and information through the production system, and identify opportunities for improvement.</li>
<li>Identify and eliminate waste in the manufacturing process, including defects, overproduction, waiting time, excess inventory, unnecessary motion, and unused talent.</li>
<li>Confirm system and product capabilities by designing feasibility and testing methods.</li>
<li>Assist to create and revise product requirement specifications.</li>
<li>Prepare product test and investigation reports by collecting, analyzing, and summarizing information.</li>
<li>Research and champion an understanding of regulatory requirements as related to mechanical engineering for SynCardia products.</li>
</ul>
Responsibility &amp; Authority Affecting Quality
<ul>
<li>Initiate action to prevent the occurrence of nonconformities relating to the product, process and Quality System.</li>
<li>Identify and record potential problems relating to the product, process and Quality System.</li>
<li>Initiate, recommend or provide solutions through designated channels.</li>
<li>Record and/or report all instances of customer feedback on product.</li>
</ul>
Requirements &amp; Education:
<ul>
<li>SolidWorks CAD software or equivalent 3D modeling software and tool design</li>
<li>Demonstrated experience in applying Lean Six Sigma methodologies to improve manufacturing processes and drive continuous improvement initiatives.</li>
<li>Experience leading manufacturing projects</li>
<li>Detailed dimensioned drawings, for components &amp; assemblies</li>
<li>Knowledge of pneumatic systems</li>
<li>Basic knowledge of mechanical measurements tools and techniques</li>
<li>Experience with geometric dimensioning and tolerancing per ASME Y14.5M</li>
<li>Excellent communication skills</li>
<li>Excellent technical writing skills</li>
<li>Strong organizational skills</li>
<li>Detail oriented</li>
<li>Ability to handle multiple tasks simultaneously</li>
<li>A team player / collaborative </li>
<li>Ability to react and learn quickly in a dynamic environment</li>
<li>Bachelor's Degree or Master's Degree, or 5 years of relevant experience in Mechanical Engineering or Biomedical Engineering</li>
<li>General understanding of mechanical design philosophies, process, tools and standards</li>
<li>Regulated device experience&nbsp;</li>
</ul>
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Senior Manufacturing Engineer - SynCardia Systems, LLC

<h3>Job Description</h3>
Job Description
​Salary: &nbsp;$120000-$135000
Other Forms of Compensation:&nbsp;&nbsp;
Pay Grade:&nbsp;8&nbsp;
Crothall Healthcare is a Compass One Company that provides specialized, high-quality, innovative, and responsive support services exclusively to the healthcare industry. Crothall serves many of the Top 100 Hospitals throughout its over 1300 healthcare service teams in 46 states. Crothall has been recognized as one of Modern Healthcare’s Best Places to Work and Best Places to Work in Pennsylvania since 2013 and Becker's Top 150 Places to Work since 2016. A division of Compass Group USA, we have more than 26,000 team members. Our core services include: Environmental Services, Healthcare Technology Solutions, Patient Transportation, Laundry &amp; Linen, Facilities Management, and Ambulatory EVS. Learn more at <a href="http://www.Crothall.com" target="_blank">www.Crothall.com</a>.
Job Summary
Key Responsibilities:
<ul>
<li>Perform planned preventive maintenance, calibrations where certification may be required and electrical safety inspections on imaging and related equipment in compliance with established standards</li>
<li>Perform major repairs by replacing defective components, readjust components to manufacturer’s specifications using appropriate tools and measuring instruments. May require certification in order to complete repairs</li>
<li>Assist with diagnostic imaging cross training of BMET Technicians</li>
<li>Confers with manufacturer’s representatives and equipment operators to resolve equipment related problems</li>
<li>Provide emergency on-call responsibilities</li>
<li>Research and initiate orders for repair parts, working within established budget parameters</li>
<li>Conducts and compiles Quality Assurance records and reports necessary for compliance with specifications and policies</li>
<li>Document all significant asset related actions in compliance with department practices</li>
<li>Must be capable of performing all the duties and responsibilities of a BMET III</li>
</ul>
Preferred Qualifications:
<ul>
<li>Associates degree in Electronics/Imaging Technology, Biomedical Equipment Technology, or military training</li>
<li>Prior experience of at least seven to ten years experience with various imaging equipment manufacturers or other appropriate related experience</li>
<li>Minimum of seven years experience in the repair of radiology equipment and prior biomedical experience</li>
<li>Should possess specialized knowledge in several specialized modalities such as radiology, MRI, nuclear medicine, ultrasound, CT, cath. lab., linear accelerators, etc. </li>
<li>Prefer certification (CRES) in these different modalities</li>
<li>Good communication and strong customer service skills</li>
<li>Ability and willingness to serve "on-call" duty as required</li>
<li>Must be willing to serve as a technical resource to others in areas of specialty or certification(s)</li>
</ul>
Apply to Crothall today!
Crothall is a member of Compass Group USA
Click here to Learn More about the Compass Story
Associates at Crothall are offered many fantastic benefits.&nbsp;
<ul>
<li>Medical</li>
<li>Dental</li>
<li>Vision</li>
<li>Life Insurance/ AD</li>
<li>Disability Insurance</li>
<li>Retirement Plan</li>
<li>Flexible Time Off</li>
<li>Holiday Time Off (varies by site/state)</li>
<li>Associate Shopping Program</li>
<li>Health and Wellness Programs</li>
<li>Discount Marketplace</li>
<li>Identity Theft Protection</li>
<li>Pet Insurance</li>
<li>Commuter Benefits</li>
<li>Employee Assistance Program</li>
<li>Flexible Spending Accounts (FSAs)</li>
</ul>
Associates may also be eligible for paid and/or unpaid time off benefits in accordance with applicable federal, state, and local laws.&nbsp;For positions in Washington State, Maryland, or to be performed Remotely, click here for paid time off benefits information.
Compass Group is an equal opportunity employer. At Compass, we are committed to treating all Applicants and Associates fairly based on their abilities, achievements, and experience without regard to race, national origin, sex, age, disability, veteran status, sexual orientation, gender identity, or any other classification protected by law.
Qualified candidates must be able to perform the essential functions of this position satisfactorily with or without a reasonable accommodation. Disclaimer: this job post is not necessarily an exhaustive list of all essential responsibilities, skills, tasks, or requirements associated with this position. While this is intended to be an accurate reflection of the position posted, the Company reserves the right to modify or change the essential functions of the job based on business necessity. We will consider for employment all qualified applicants, including those with a criminal history (including relevant driving history), in a manner consistent with all applicable federal, state, and local laws, including the City of Los Angeles’ Fair Chance Initiative for Hiring Ordinance, the San Francisco Fair Chance Ordinance, and the New York Fair Chance Act. We encourage applicants with a criminal history (and driving history) to apply.
Applications are accepted on an ongoing basis.
Crothall maintains a drug-free workplace.
Req ID:&nbsp;1400742
Crothall Healthcare&nbsp;
ASHLEY VAVROCK&nbsp;
[[req_classification]]&nbsp;

Imaging Service Engineer III

<h3>Job Description</h3>
Job Description
General Summary:

The Operations Engineer is responsible for equipment, facility, and utility (EFU) lifecycle management. This includes managing the specification, procurement, installation, and commissioning of new EFU assets; contributing to the development of calibration, maintenance, operation, and cleaning procedures; providing technical support to end user, quality, and maintenance personnel; and managing the decommissioning of EFU assets to be retired. The Operations Engineer is quality-centered and follows company standard operating procedures (SOPs) geared toward FDA and other applicable regulations and in-line with current good manufacturing practices (cGMPs).

Essential Duties and Responsibilities: 
<ul>
<li>Manage the development of EFU user requirement specifications (URS) and functional requirement specifications (FRS).</li>
<li>Assess the impact of EFU on cGMP compliance and patient health and safety.</li>
<li>Author, execute, review, and/or approve commissioning plan, factory acceptance test (FAT), and site acceptance test (SAT) documents.</li>
<li>Assimilate information from regulatory, guidance, and technical documents; EFU manufacturers and service personnel; and Cytovance resources to create operation, calibration, and preventive maintenance procedures.</li>
<li>Train end user, quality, and maintenance personnel on EFU procedures.</li>
<li>Create and maintain engineering drawings.</li>
<li>Assist in the administration of EFU software packages (ex. CMMS, SCADA, etc.).</li>
<li>Provide technical troubleshooting and creative solutions to manufacturing process challenges.</li>
<li>Provide support during regulatory inspections and customer audits. Identify and implement quality system improvements when gaps are identified through audits and departmental reviews. </li>
<li>May provide direction to junior personnel on an as needed basis but has no formal reports</li>
<li>Additional duties as assigned</li>
</ul>
Job Requirements:

<ul>
<li>Bachelor’s degree in an applicable engineering discipline (ex. chemical, biomedical, mechanical, electrical, etc.) with 0-2 years professional experience in a biologics/pharmaceutical (clinical development or commercial manufacturing) environment.</li>
</ul>
OR
Associate’s degree in an applicable discipline with 3-5 years professional experience in a biologics/pharmaceutical (clinical development or commercial manufacturing) environment.
<ul>
<li>Performance of Essential Duties and Responsibilities for low-complexity unit operations with moderate input from management and moderate-complexity unit operations with high input from management.</li>
<li>Excellent written and verbal communication skills.</li>
<li>Ability to adapt to changing regulatory, client, and company requirements; new technologies; and shifting priorities.</li>
<li>Ability to travel (typically &lt;5%) for training and/or EFU testing</li>
<li>Ability to work flexible hours and inconsistent schedules as necessary to meet production demands and timelines.</li>
</ul>
Physical Demands: 
 While performing the duties of this Job, the employee is regularly required to stand and talk or hear. The employee is frequently required to use hands to finger, handle, or feel and reach with hands and arms. The employee is occasionally required to walk; sit; climb or balance and stoop, kneel, crouch, or crawl. The employee must occasionally lift and/or move up to 50 pounds. 

Work Environment: 

Work environment will vary to include: office atmosphere, clean room aseptic manufacturing areas, mechanical utility spaces, walk in cold/warm/freezer rooms, warehouse, and outside (ex. roof). Environmental conditions will include moderate temperature fluctuations, moderate humidity, and moderate noise levels. Close proximity to hazardous utilities, fumes, or chemicals is possible. While performing the duties of this job, the employee is occasionally exposed to moving mechanical parts; toxic or caustic chemicals.

Operations Engineer I

<h3>Job Description</h3>
Job Description
​Salary: &nbsp;$115000-$130000
Other Forms of Compensation:&nbsp;&nbsp;
Pay Grade:&nbsp;8&nbsp;
Crothall Healthcare is a Compass One Company that provides specialized, high-quality, innovative, and responsive support services exclusively to the healthcare industry. Crothall serves many of the Top 100 Hospitals throughout its over 1300 healthcare service teams in 46 states. Crothall has been recognized as one of Modern Healthcare’s Best Places to Work and Best Places to Work in Pennsylvania since 2013 and Becker's Top 150 Places to Work since 2016. A division of Compass Group USA, we have more than 26,000 team members. Our core services include: Environmental Services, Healthcare Technology Solutions, Patient Transportation, Laundry &amp; Linen, Facilities Management, and Ambulatory EVS. Learn more at <a href="http://www.Crothall.com" target="_blank">www.Crothall.com</a>.
Job Summary
Key Responsibilities:
<ul>
<li>Perform planned preventive maintenance, calibrations where certification may be required and electrical safety inspections on imaging and related equipment in compliance with established standards</li>
<li>Perform major repairs by replacing defective components, readjust components to manufacturer’s specifications using appropriate tools and measuring instruments. May require certification in order to complete repairs</li>
<li>Assist with diagnostic imaging cross training of BMET Technicians</li>
<li>Confers with manufacturer’s representatives and equipment operators to resolve equipment related problems</li>
<li>Provide emergency on-call responsibilities</li>
<li>Research and initiate orders for repair parts, working within established budget parameters</li>
<li>Conducts and compiles Quality Assurance records and reports necessary for compliance with specifications and policies</li>
<li>Document all significant asset related actions in compliance with department practices</li>
<li>Must be capable of performing all the duties and responsibilities of a BMET III</li>
</ul>
Preferred Qualifications:
<ul>
<li>Associates degree in Electronics/Imaging Technology, Biomedical Equipment Technology, or military training</li>
<li>Prior experience of at least seven to ten years experience with various imaging equipment manufacturers or other appropriate related experience</li>
<li>Minimum of seven years experience in the repair of radiology equipment and prior biomedical experience</li>
<li>Should possess specialized knowledge in several specialized modalities such as radiology, MRI, nuclear medicine, ultrasound, CT, cath. lab., linear accelerators, etc. </li>
<li>Prefer certification (CRES) in these different modalities</li>
<li>Good communication and strong customer service skills</li>
<li>Ability and willingness to serve "on-call" duty as required</li>
<li>Must be willing to serve as a technical resource to others in areas of specialty or certification(s)</li>
</ul>
Apply to Crothall today!
Crothall is a member of Compass Group USA
Click here to Learn More about the Compass Story
Associates at Crothall are offered many fantastic benefits.&nbsp;
<ul>
<li>Medical</li>
<li>Dental</li>
<li>Vision</li>
<li>Life Insurance/ AD</li>
<li>Disability Insurance</li>
<li>Retirement Plan</li>
<li>Flexible Time Off</li>
<li>Holiday Time Off (varies by site/state)</li>
<li>Associate Shopping Program</li>
<li>Health and Wellness Programs</li>
<li>Discount Marketplace</li>
<li>Identity Theft Protection</li>
<li>Pet Insurance</li>
<li>Commuter Benefits</li>
<li>Employee Assistance Program</li>
<li>Flexible Spending Accounts (FSAs)</li>
</ul>
Associates may also be eligible for paid and/or unpaid time off benefits in accordance with applicable federal, state, and local laws.&nbsp;For positions in Washington State, Maryland, or to be performed Remotely, click here for paid time off benefits information.
Compass Group is an equal opportunity employer. At Compass, we are committed to treating all Applicants and Associates fairly based on their abilities, achievements, and experience without regard to race, national origin, sex, age, disability, veteran status, sexual orientation, gender identity, or any other classification protected by law.
Qualified candidates must be able to perform the essential functions of this position satisfactorily with or without a reasonable accommodation. Disclaimer: this job post is not necessarily an exhaustive list of all essential responsibilities, skills, tasks, or requirements associated with this position. While this is intended to be an accurate reflection of the position posted, the Company reserves the right to modify or change the essential functions of the job based on business necessity. We will consider for employment all qualified applicants, including those with a criminal history (including relevant driving history), in a manner consistent with all applicable federal, state, and local laws, including the City of Los Angeles’ Fair Chance Initiative for Hiring Ordinance, the San Francisco Fair Chance Ordinance, and the New York Fair Chance Act. We encourage applicants with a criminal history (and driving history) to apply.
Applications are accepted on an ongoing basis.
Crothall maintains a drug-free workplace.
Req ID:&nbsp;1400473
Crothall Healthcare&nbsp;
ASHLEY VAVROCK&nbsp;
[[req_classification]]&nbsp;

<h3>Job Description</h3>
Job Description
​Salary: &nbsp;
Other Forms of Compensation:&nbsp;&nbsp;
Pay Grade:&nbsp;6&nbsp;
Crothall Healthcare is a Compass One Company that provides specialized, high-quality, innovative, and responsive support services exclusively to the healthcare industry. Crothall serves many of the Top 100 Hospitals throughout its over 1300 healthcare service teams in 46 states. Crothall has been recognized as one of Modern Healthcare’s Best Places to Work and Best Places to Work in Pennsylvania since 2013 and Becker's Top 150 Places to Work since 2016. A division of Compass Group USA, we have more than 26,000 team members. Our core services include: Environmental Services, Healthcare Technology Solutions, Patient Transportation, Laundry &amp; Linen, Facilities Management, and Ambulatory EVS. Learn more at <a href="http://www.Crothall.com" target="_blank">www.Crothall.com</a>.
Job Summary
Key Responsibilities:
<ul>
<li>Perform planned preventive maintenance, calibrations where certification may be required and electrical safety inspections on imaging and related equipment in compliance with established standards</li>
<li>Perform major repairs by replacing defective components, readjust components to manufacturer’s specifications using appropriate tools and measuring instruments. May require certification in order to complete repairs</li>
<li>Assist with diagnostic imaging cross training of BMET Technicians</li>
<li>Confers with manufacturer’s representatives and equipment operators to resolve equipment related problems</li>
<li>Provide emergency on-call responsibilities</li>
<li>Research and initiate orders for repair parts, working within established budget parameters</li>
<li>Conducts and compiles Quality Assurance records and reports necessary for compliance with specifications and policies</li>
<li>Document all significant asset related actions in compliance with department practices</li>
<li>Must be capable of performing all the duties and responsibilities of a BMET III</li>
</ul>
Preferred Qualifications:
<ul>
<li>Associates degree in Electronics/Imaging Technology, Biomedical Equipment Technology, or military training</li>
<li>Prior experience of at least two years experience with various imaging equipment manufacturers or other appropriate related experience</li>
<li>Minimum of two years experience in the repair of radiology equipment and prior biomedical experience</li>
<li>Should possess specialized knowledge in several specialized modalities such as radiology, MRI, nuclear medicine, ultrasound, CT, cath. lab., linear accelerators, etc. </li>
<li>Prefer certification (CRES) in these different modalities</li>
<li>Good communication and strong customer service skills</li>
<li>Ability and willingness to serve "on-call" duty as required</li>
<li>Must be willing to serve as a technical resource to others in areas of specialty or certification(s)</li>
</ul>
Apply to Crothall today!
Crothall is a member of Compass Group USA
Click here to Learn More about the Compass Story
Associates at Crothall are offered many fantastic benefits.&nbsp;
<ul>
<li>Medical</li>
<li>Dental</li>
<li>Vision</li>
<li>Life Insurance/ AD</li>
<li>Disability Insurance</li>
<li>Retirement Plan</li>
<li>Flexible Time Off</li>
<li>Holiday Time Off (varies by site/state)</li>
<li>Associate Shopping Program</li>
<li>Health and Wellness Programs</li>
<li>Discount Marketplace</li>
<li>Identity Theft Protection</li>
<li>Pet Insurance</li>
<li>Commuter Benefits</li>
<li>Employee Assistance Program</li>
<li>Flexible Spending Accounts (FSAs)</li>
<li>Paid Parental Leave</li>
<li>Personal Leave</li>
</ul>
Associates may also be eligible for paid and/or unpaid time off benefits in accordance with applicable federal, state, and local laws.&nbsp;For positions in Washington State, Maryland, or to be performed Remotely, click here for paid time off benefits information.
Compass Group is an equal opportunity employer. At Compass, we are committed to treating all Applicants and Associates fairly based on their abilities, achievements, and experience without regard to race, national origin, sex, age, disability, veteran status, sexual orientation, gender identity, or any other classification protected by law.
Qualified candidates must be able to perform the essential functions of this position satisfactorily with or without a reasonable accommodation. Disclaimer: this job post is not necessarily an exhaustive list of all essential responsibilities, skills, tasks, or requirements associated with this position. While this is intended to be an accurate reflection of the position posted, the Company reserves the right to modify or change the essential functions of the job based on business necessity. We will consider for employment all qualified applicants, including those with a criminal history (including relevant driving history), in a manner consistent with all applicable federal, state, and local laws, including the City of Los Angeles’ Fair Chance Initiative for Hiring Ordinance, the San Francisco Fair Chance Ordinance, and the New York Fair Chance Act. We encourage applicants with a criminal history (and driving history) to apply.
Applications are accepted on an ongoing basis.
Crothall maintains a drug-free workplace.
Req ID:&nbsp;1408201
Crothall Healthcare&nbsp;
ASHLEY VAVROCK&nbsp;
[[req_classification]]&nbsp;

Imaging Service Engineer I

<h3>Job Description</h3>
Job DescriptionSalary: 
Our mission is to Profoundly change the standard of care by creating a tomorrow where clinicians can confidently ablate tissue with precision; a tomorrow where patients have access to safe and effective treatment options, so they can quickly return to their daily lives. Changing the standard of care is part of our fabric. We are a group of energetic, problem-solvers focused on innovation and looking to change the world. We are changing the paradigm for treating diseases such as prostate cancer by using real-time MR Imaging, thermal ultrasound and close-loop temperature feedback control, to gently ablate the diseased tissue with minimal side effects.
 
If you share our values and want to work in a collaborative results-focused culture and want to make a profound impact in healthcare and your career, here is your chance.
 
General Accountability:
The Field Service Engineer provides onsite support primarily in the U.S., through maintenance and troubleshooting services. From these visits, they will recommend parts and service solutions to improve machine uptime, maintenance and operation. When not traveling, the Field Service Engineer will perform proactive service tasks including, but not limited to, troubleshoot customer issues via telephone, email and online meetings, prepare spare parts quotes, order entry, and customer follow-up.
 
Duties and Responsibilities:
<ul>
<li>Perform and support all installation activities for Profound Products including but not limited to site assessments, installations, maintenance and troubleshooting.</li>
<li>Conduct MR testing to support product development activities (typically at hospital sites during off-hours, schedule and travel flexibility is a requirement).</li>
<li>Act as the primary link between customer and Profound as needed.</li>
<li>Document service records and activities according to the company QMS processes for service visits and upgrades deployed to the field.</li>
<li>Perform calibration of company products as required.</li>
<li>Execute test protocols, troubleshooting protocols for hardware, software and systems aspects of the companys products</li>
<li>Investigate methods of increasing efficiency in MR testing and development activities.</li>
<li>Regularly participate in MRI phantom testing activities for new product revisions.</li>
<li>Support executing and improvement of field service strategy for Profound products.</li>
<li>Organize and prioritize schedule in accordance with customer requirements to determine needs for immediate attention, onsite visits, and remote assistance</li>
<li>When required, enter parts orders, generate and follow-up parts quotes</li>
<li>Work with IT departments at customer sites for proper equipment networking </li>
<li>Contribute to the establishment of a professional service team at the company</li>
<li>Responsible for creating documentation and electronic reference material to support the field service of products. Specifically, installation and troubleshooting manuals.</li>
<li>Participate in product design activities representing design for serviceability and product quality representing both internal customers and end users</li>
<li>Interact with the engineering, quality and operations team to drive the resolution of technical issues</li>
<li>Executes other ad-hoc projects as assigned by manager.</li>
</ul>
Education and Certification:
<ul>
<li>B.S. in Biomedical Engineering , Biotech, Electrical Engineering, or Electronics related fields or equivalent experience.</li>
</ul>
 
Key Attributes (experience, skills and technical knowledge):
<ul>
<li> Ability to travel on short notice in the US 80% of the time.</li>
<li> Excellent customer focus with ability to reliably respond to inquiries, communicate and interact with health care professionals and Scientists that possess advanced Degree</li>
<li> Previous field service experience is desirable.</li>
<li> Experience with MRI operations is desirable.</li>
<li> Strong multi-tasking skills, self-sufficiency, resourcefulness is a must for this exciting, fast paced environment.</li>
<li> Good critical thinking and analytical troubleshooting and problem skills </li>
<li> Demonstrated ability to work as part of a team and independently with strong initiative and accountability.</li>
<li> Excellent verbal, written, MS Office, computer, technical data, and networking communication and presentation skills, with ability to communicate complex technical issues in an easy to understand manner</li>
<li> Excellent organizational skills with ability to follow through, and meet deadlines within an entrepreneurial and customer-focused work environment </li>
<li> Working knowledge of quality management systems (ISO 9001 or ISO 13485)</li>
<li> Exemplify willingness and flexibility in working differing time shifts to accommodate customer needs.</li>
<li> Working knowledge of operating multiple OEM MRIs is an asset.</li>
</ul>
 
We thank you for your interest in Profound Medical. Please note only candidates that are short-listed will be contacted.
 
We strive to promote diversity and equal opportunity in the workplace and encourage applications from all qualified individuals, including those with disabilities. If selected to participate in the recruitment, selection, and/or assessment process, please inform Human Resources of the nature of any accommodation(s) that you may require.
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