10 Ge Healthcare jobs in Barrington
Senior Product Development Engineer - Medical Devices
Posted today
Job Viewed
Job Description
Do you have a passion for designing and developing innovative medical and drug delivery devices that help improve lives? At Gilero’s Chicago, IL office, we are looking for a Senior Product Development Engineer to join our mission-driven team driving innovative solutions for patients and customers. In this role you will champion the design, development, and production of medical devices and combination devices, focusing on idea generation, verification, validation, and DHF development to state-of-the-art requirements.
If you thrive in a fast-paced, collaborative environment and like ensuing high-quality outcomes working with customers, vendors, and internal teams, this is the opportunity for you. Join us and be part of a company that values innovation, integrity, and excellence!
Responsibilities
- Act as a technical lead, increasing the rigor of technical product development, with project oversight of products, accessories, and cross-functional initiatives.
- Manage product development deliverables of high complexity through the entire development lifecycle, concept through manufacturing transfer (Phase 0 – 5).
- Track technical risk and provide engineering guidance.
- Provide feedback and mentorship to junior engineers.
- Lead the development team through technical risk retirement. Guide the team on technical risks through step-by-step simplification to discover root cause.
- Create, review, and release documents according to Gilero’s QMS and the lifecycle of the project and develop test methods and protocols to fulfill state of the art requirements.
- Inform project managers and business development on technical projects variables in order to build accurate project budgets that include feasibility, prototyping, verification and validation.
- Act as project manager for smaller, technically oriented projects.
Skills/Qualifications:
- BS in Engineering or equivalent technical degree
- 5+ years of product development experience in medical device, combination product or similar space preferred.
- Skilled at transforming complex situations into well-defined project deliverables
- Able to lead team to achieve difficult goals through step by step simplification
- Able to convert complex questions into tasks to further drive simplification and clarification.
- Understanding of good GDP
- Understand the Phase Gate System
- Have deep ISO 14971, 13485 and CFR 21 Knowledge base; Experience with ISO 10993 a plus.
- Translate VOC (Voice of Customer) feedback into engineering design inputs and outputs.
- Create/draft clinically relevant User Requirements with minimal oversight
- Ability to translate User Needs/Requirements into measurable technical/product requirements and set appropriate specification though thought experiments and empirical testing.
- Ability to discern and document appropriate scenarios for rationale-based decisions versus testing based approaches
- Ability to author scientific/logic based rationale
- Prepare documentation to support design history files and regulatory submissions
- Analyze test data, interpret results, formulate conclusions, and apply statistical techniques (t-test, ANOVA, UCL/LCL, Tolerance Intervals)
- Draft Risk documentation through understanding of Risk, Risk analysis, & Risk Burn Down
- Support chartering and maintaining project objectives and milestones.
- Develop testing campaigns, test flows, sample size analysis, and justification, based on sound judgment, Risk analysis, and QMS requirements.
- Lead product and process risk assessments, including hazard analysis, FMEAs and residual risk analysis in conjunction with Quality Engineering
- Write and execute protocols for design verification and validation
- Lead test method development and validation, have strong knowledge of measurement system analysis (e.g. calibration, accuracy, gage R&R, etc)
- Oversee and perform testing and inspection of prototypes and pre-production products including assisting assembly for DV&V builds and clinical builds
- Lead investigation of device failures, coordinate resources, determine root cause, identify corrective actions, and document in conjunction with Quality Engineering
- Investigate, evaluate, and research competitive devices and product materials/designs
- Understanding of Pre-clinical validation and GLP
- Ability to review and understand technical drawings and GD&T to support development lifecycle
- Ability to review, understand, and distill technical standards (ISO, ASTM, IEC, etc).
Personal Attributes:
Meets Gilero Core Values:
- Collaboration - embracing teamwork and transparency in our organization, partnering with our customers and vendors
- Integrity - doing the right thing at all times; fair and trustworthy; always keeping the patient in mind
- Innovation - open to new ideas, processes, and solutions; leveraging technology to creatively solve problems
- Excellence - delivering exceptional products and services with passion and pride
- Comfortable and productive in a fast-paced, entrepreneurial environment
- A self-starter seeking a career opportunity with potential for internal advancement, seeking responsibility for core activities and providing high quality service to internal and to external clients
- Commitment to excellence and quality service to external and internal customer
- Follows established policies and procedures, while contributing to continuous improvements
- Excellent communication skills (oral and written)
Why work at Gilero?
Founded in 2002, Gilero, a Sanner Group company, is an international contract engineering firm that specializes in the design, development, and manufacturing of novel medical devices and drug delivery products. At Gilero we are proud of the culture we have built that directly reflects our values of excellence, integrity, innovation, and collaboration. Motivated by our purpose to benefit people and improve patient outcomes, our team continue to grow at a rapid pace. US locations include Carlsbad, CA; Chicago, IL; as well as NC locations in Raleigh, Durham, Greensboro, and Pittsboro.
You will enjoy an annual bonus plan, Medical (3 BCBS plans to choose from), Guardian dental and vision, company provided life insurance, short-term and long-term disability, 401(k) with a match the first month you start with a zero-vesting period, and access to LinkedIn learning for personal and professional development.
Senior Product Development Engineer - Medical Devices (Chicago)
Posted 1 day ago
Job Viewed
Job Description
Do you have a passion for designing and developing innovative medical and drug delivery devices that help improve lives? At Gileros Chicago, IL office, we are looking for a Senior Product Development Engineer to join our mission-driven team driving innovative solutions for patients and customers. In this role you will champion the design, development, and production of medical devices and combination devices, focusing on idea generation, verification, validation, and DHF development to state-of-the-art requirements.
If you thrive in a fast-paced, collaborative environment and like ensuing high-quality outcomes working with customers, vendors, and internal teams, this is the opportunity for you. Join us and be part of a company that values innovation, integrity, and excellence!
Responsibilities
- Act as a technical lead, increasing the rigor of technical product development, with project oversight of products, accessories, and cross-functional initiatives.
- Manage product development deliverables of high complexity through the entire development lifecycle, concept through manufacturing transfer (Phase 0 5).
- Track technical risk and provide engineering guidance.
- Provide feedback and mentorship to junior engineers.
- Lead the development team through technical risk retirement. Guide the team on technical risks through step-by-step simplification to discover root cause.
- Create, review, and release documents according to Gileros QMS and the lifecycle of the project and develop test methods and protocols to fulfill state of the art requirements.
- Inform project managers and business development on technical projects variables in order to build accurate project budgets that include feasibility, prototyping, verification and validation.
- Act as project manager for smaller, technically oriented projects.
Skills/Qualifications:
- BS in Engineering or equivalent technical degree
- 5+ years of product development experience in medical device, combination product or similar space preferred.
- Skilled at transforming complex situations into well-defined project deliverables
- Able to lead team to achieve difficult goals through step by step simplification
- Able to convert complex questions into tasks to further drive simplification and clarification.
- Understanding of good GDP
- Understand the Phase Gate System
- Have deep ISO 14971, 13485 and CFR 21 Knowledge base; Experience with ISO 10993 a plus.
- Translate VOC (Voice of Customer) feedback into engineering design inputs and outputs.
- Create/draft clinically relevant User Requirements with minimal oversight
- Ability to translate User Needs/Requirements into measurable technical/product requirements and set appropriate specification though thought experiments and empirical testing.
- Ability to discern and document appropriate scenarios for rationale-based decisions versus testing based approaches
- Ability to author scientific/logic based rationale
- Prepare documentation to support design history files and regulatory submissions
- Analyze test data, interpret results, formulate conclusions, and apply statistical techniques (t-test, ANOVA, UCL/LCL, Tolerance Intervals)
- Draft Risk documentation through understanding of Risk, Risk analysis, & Risk Burn Down
- Support chartering and maintaining project objectives and milestones.
- Develop testing campaigns, test flows, sample size analysis, and justification, based on sound judgment, Risk analysis, and QMS requirements.
- Lead product and process risk assessments, including hazard analysis, FMEAs and residual risk analysis in conjunction with Quality Engineering
- Write and execute protocols for design verification and validation
- Lead test method development and validation, have strong knowledge of measurement system analysis (e.g. calibration, accuracy, gage R&R, etc)
- Oversee and perform testing and inspection of prototypes and pre-production products including assisting assembly for DV&V builds and clinical builds
- Lead investigation of device failures, coordinate resources, determine root cause, identify corrective actions, and document in conjunction with Quality Engineering
- Investigate, evaluate, and research competitive devices and product materials/designs
- Understanding of Pre-clinical validation and GLP
- Ability to review and understand technical drawings and GD&T to support development lifecycle
- Ability to review, understand, and distill technical standards (ISO, ASTM, IEC, etc).
Personal Attributes:
Meets Gilero Core Values:
- Collaboration - embracing teamwork and transparency in our organization, partnering with our customers and vendors
- Integrity - doing the right thing at all times; fair and trustworthy; always keeping the patient in mind
- Innovation - open to new ideas, processes, and solutions; leveraging technology to creatively solve problems
- Excellence - delivering exceptional products and services with passion and pride
- Comfortable and productive in a fast-paced, entrepreneurial environment
- A self-starter seeking a career opportunity with potential for internal advancement, seeking responsibility for core activities and providing high quality service to internal and to external clients
- Commitment to excellence and quality service to external and internal customer
- Follows established policies and procedures, while contributing to continuous improvements
- Excellent communication skills (oral and written)
Why work at Gilero?
Founded in 2002, Gilero, a Sanner Group company, is an international contract engineering firm that specializes in the design, development, and manufacturing of novel medical devices and drug delivery products. At Gilero we are proud of the culture we have built that directly reflects our values of excellence, integrity, innovation, and collaboration. Motivated by our purpose to benefit people and improve patient outcomes, our team continue to grow at a rapid pace. US locations include Carlsbad, CA; Chicago, IL; as well as NC locations in Raleigh, Durham, Greensboro, and Pittsboro.
You will enjoy an annual bonus plan, Medical (3 BCBS plans to choose from), Guardian dental and vision, company provided life insurance, short-term and long-term disability, 401(k) with a match the first month you start with a zero-vesting period, and access to LinkedIn learning for personal and professional development.
Senior Product Marketing Specialist - Healthcare Solutions

Posted 1 day ago
Job Viewed
Job Description
**OVERVIEW**
You will work in concert with the product management team to analyze market conditions, the competitive landscape, customer needs, and develop go-to-market plans that differentiate Clinical Effectiveness (CE) products from the competition while reinforcing customer value. You also will support the sales and client service teams through the creation of messaging, tools and sales support material, and will drive strategy and subject matter expertise for campaigns and communications to be delivered by the marketing communications team. You work closely with portfolio marketing, product management, strategic marketing communications, training and sales to deliver accelerated growth for CE products.
**RESPONSIBILITIES**
+ **Market Intelligence:** understand CE market trends, customer needs, and competitive landscape. Use this knowledge to inform sales enablement and go-to-market strategies.
+ **Product Positioning:** develop clear and compelling product positioning and messaging that differentiates our products in the market.
+ **Content Creation:** create and manage a variety of content (e.g., sales documentation, product videos, website copy, blog posts) to articulate the benefits of our products to enterprise businesses.
+ **Sales Enablement:** equip the sales team with the necessary tools and materials to sell our products effectively. This includes training sessions, product collateral, and custom sales strategies.
+ **Partner Enablement:** support the partner ecosystem with the necessary tools and materials to sell our products effectively.
+ **Analyst Support:** create differentiated messaging & materials for analyst briefings, inquiries, and RFPs.
+ **Stakeholder Engagement:** collaborate with internal teams (e.g., product management, sales, customer success) and external stakeholders (e.g., customers, partners, industry analysts) to maximize product impact.
**QUALIFICATIONS**
**Education:** Bachelor's degree from an accredited four-year college or university in relevant field or equivalent
**Experience:** Five or more years in product marketing or related experience
**Preferred:**
+ Working with sales, account management and customer success functions
+ Understanding of SaaS products and their application in business
+ Working with marketing enterprise software solutions
+ Experience in creating marketing collateral & sales enablement tools
+ Experience in healthcare technology or similar setting a plus
**TRAVEL:** Up to 10% travel required as necessary, mostly to internal meetings
#LI-Hybrid
_Applicants may be required to appear onsite at a Wolters Kluwer office as part of the recruitment process._
**Compensation:**
Target salary range CA, CT, CO, DC, HI, IL, MD, MN, NY, RI, WA: $95,560 - $133,750
EQUAL EMPLOYMENT OPPORTUNITY Wolters Kluwer U. S. Corporation and all of its subsidiaries, divisions and customer/business units is an Equal Opportunity / Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.
Senior Product Marketing Specialist - Healthcare Solutions

Posted 1 day ago
Job Viewed
Job Description
**OVERVIEW**
You will work in concert with the product management team to analyze market conditions, the competitive landscape, customer needs, and develop go-to-market plans that differentiate Clinical Effectiveness (CE) products from the competition while reinforcing customer value. You also will support the sales and client service teams through the creation of messaging, tools and sales support material, and will drive strategy and subject matter expertise for campaigns and communications to be delivered by the marketing communications team. You work closely with portfolio marketing, product management, strategic marketing communications, training and sales to deliver accelerated growth for CE products.
**RESPONSIBILITIES**
+ **Market Intelligence:** understand CE market trends, customer needs, and competitive landscape. Use this knowledge to inform sales enablement and go-to-market strategies.
+ **Product Positioning:** develop clear and compelling product positioning and messaging that differentiates our products in the market.
+ **Content Creation:** create and manage a variety of content (e.g., sales documentation, product videos, website copy, blog posts) to articulate the benefits of our products to enterprise businesses.
+ **Sales Enablement:** equip the sales team with the necessary tools and materials to sell our products effectively. This includes training sessions, product collateral, and custom sales strategies.
+ **Partner Enablement:** support the partner ecosystem with the necessary tools and materials to sell our products effectively.
+ **Analyst Support:** create differentiated messaging & materials for analyst briefings, inquiries, and RFPs.
+ **Stakeholder Engagement:** collaborate with internal teams (e.g., product management, sales, customer success) and external stakeholders (e.g., customers, partners, industry analysts) to maximize product impact.
**QUALIFICATIONS**
**Education:** Bachelor's degree from an accredited four-year college or university in relevant field or equivalent
**Experience:** Five or more years in product marketing or related experience
**Preferred:**
+ Working with sales, account management and customer success functions
+ Understanding of SaaS products and their application in business
+ Working with marketing enterprise software solutions
+ Experience in creating marketing collateral & sales enablement tools
+ Experience in healthcare technology or similar setting a plus
**TRAVEL:** Up to 10% travel required as necessary, mostly to internal meetings
#LI-Hybrid
_Applicants may be required to appear onsite at a Wolters Kluwer office as part of the recruitment process._
**Compensation:**
Target salary range CA, CT, CO, DC, HI, IL, MD, MN, NY, RI, WA: $95,560 - $133,750
EQUAL EMPLOYMENT OPPORTUNITY Wolters Kluwer U. S. Corporation and all of its subsidiaries, divisions and customer/business units is an Equal Opportunity / Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.
Solutions Architect, Healthcare Integrations (Chicago, IL)
Posted 9 days ago
Job Viewed
Job Description
Hippocratic AI is developing the first safety-focused Large Language Model (LLM) for healthcare. Our mission is to dramatically improve healthcare accessibility and outcomes by bringing deep healthcare expertise to every person. No other technology has the potential for this level of global impact on health.
Why Join Our Team
- Innovative mission: We are creating a safe, healthcare-focused LLM that can transform health outcomes on a global scale.
- Visionary leadership: Hippocratic AI was co-founded by CEO Munjal Shah alongside physicians, hospital administrators, healthcare professionals, and AI researchers from top institutions including El Camino Health, Johns Hopkins, Washington University in St. Louis, Stanford, Google, Meta, Microsoft and NVIDIA.
- Strategic investors: We have raised a total of $278 million in funding, backed by top investors such as Andreessen Horowitz, General Catalyst, Kleiner Perkins, NVIDIA's NVentures, Premji Invest, SV Angel, and six health systems.
- Team and expertise: We are working with top experts in healthcare and artificial intelligence to ensure the safety and efficacy of our technology.
We value in-person teamwork and believe the best ideas happen together. Our team is expected to be in the office five days a week in Chicago, IL.
Location:
WeWork - One South Dearborn (Loop)
- Address: 1 S Dearborn St, Chicago, IL
- Right in the Loop (Downtown), super central
We are seeking a dynamic and experienced Solution Architect to drive the integration and deployment of our advanced AI agents across healthcare organizations - including payors, providers, and digital health companies. In this role, you will partner directly with customers to deeply understand their operational workflows, identify and translate their technical requirements into effective AI-powered conversations, and guide them through setting up integrations and deploying agents.
You will serve as the technical backbone of our client relationships. From defining integration requirements to building and launching conversational AI agents that enhance patient care, you will have a pivotal impact on our product, customer success, and ultimately, patient outcomes.
Key Responsibilities
- Customer Workflow Discovery : Partner with customers to analyze and document their operational workflows, translating these into integration specifications and AI conversation designs.
- Integration Architecture : Define, document, and drive the technical architecture required to connect our solutions with client EHR systems, CRMs, population health tools, and other relevant platforms.
- AI Agent Design & Deployment : Design, customize, and deploy modular, scalable AI agents that align with the customer's unique needs and use cases.
- Technical Project Leadership : Lead and manage the technical post-sale implementation process, acting as the primary technical contact and ensuring a seamless deployment.
- Cross-Functional Collaboration : Work closely with engineering, product, machine learning, clinical, and sales teams to develop solutions to meet our customer' needs.
- Tooling & Process Automation : Develop reusable tooling, playbooks, and repeatable frameworks to improve implementation scalability and efficiency.
- Bachelor's or Master's degree in Computer Science, Business or a related field
- Minimum of 5 years of experience in healthcare implementation or product management.
- Minimum of 5 years of experience integrating with enterprise EHRs (Epic, Cerner, Athena, etc.) or payers / digital health companies.
- Familiarity with healthcare data and interoperability standards (such as FHIR, HL7v2, etc.).
- Experience with ancillary healthcare integrations, including population health systems, CRM, ERP, etc.
- Proven ability to cultivate strong customer relationships and deliver exemplary product support.
- Demonstrated proficiency in translating external stakeholder needs into internal product requirements.
- Comfortable reading and debugging Python.
- Start-up experience preferred.
***Be aware of recruitment scams impersonating Hippocratic AI. All recruiting communication will come from @hippocraticai.com email addresses. We will never request payment or sensitive personal information during the hiring process. If anything appears suspicious, stop engaging immediately and report the incident.
Medical Equipment Repairer - Medical
Posted today
Job Viewed
Job Description
Medical Equipment Maintenance
Posted today
Job Viewed
Job Description
The Maintenance Person assists management in achieving and maintaining outstanding interior and exterior restaurant cleanliness and maintaining restaurant equipment. As a member of the Maintenance Team, your restaurant will support you with the tools and training needed to succeed. You must be at least 18 years of age or older to be considered.
The Maintenance Person's responsibilities may include, but are not limited to:
* Filtering oil fryers daily
* Maintaining outside grounds
* Clean equipment, inside and outside windows, stock rooms and restrooms
* Unload delivery truck 2 times a week
* Take out and empty trash compactor
* Change light bulbs
* Clean HVAC/Exhaust units and roof of debris
Additional Info:
* paid vacation
* Education through Archways to Opportunity including opportunities to earn a High School degree, college tuition assistance and English classes as a second language
* Medical, dental and vision coverage
* Pre-tax flexible spending accounts
* Short- and Long-Term Disability, life and accident insurance
* Service awards
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Engineering Technician (Medical Device Technology) - Entry/Junior Level
Posted today
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Job Description
Job ID:
We're currently seeking entry/junior level Engineering Technicians who have an interest in the medical device/technology industry. These are all onsite roles (5 days/week) and we're open to either fresh Bachelor graduates with internship experience or those with an Associate's degree and a year of experience working within and engineering lab environment. See below for other details!
Day to Day Responsibilities:
- 50% manual, handling pumps
- 50% taking observations, pull log files of pump (records of what occurred)
- Interacting with a lot of equipment - microscopes, strength and contention testing devices, electrical equipment, etc.
Top Skills Needed:
- Lab experience, collecting data, following procedures (will be trained on documentation practices, lab safety practices, the testing products) but need to be able to read and follow procedures- required
- Writing or developing scripts for electrical mechanical devices- a plus
- Handling electrical mechanical devices, interact with device- a plus
- Softwares: Microsoft, Windows- required (Script, Macro, Programming, Writing preferred)
Responsibilities:
- This position is primarily responsible for the electrical, mechanical, and environmental testing and evaluation of new and existing Electromechanical medical devices. Will be required to handle test stands, set-up, perform and monitor testing activities.
- Testing products in the Reliability Test Lab to test requirements specified by Product and Reliability Engineering.
- Taking direction from the Reliability Test Manager, Lab Supervisor and Test Engineers on safe working procedures, use of equipment, recording of test data, and monitoring of results.
- Performing all tests as directed by the Reliability Test Manager, Lab Supervisor and Test Engineers.
- Providing accurate and timely documented results.
- Communicating test results to appropriate engineering personnel.
- Performing teardown destructive testing or test to failure activities as part of the product development process.
- Verifying and validating proposed and/or implemented changes to existing products. Performing specified tests of competitive products as part of the new product development process.
- Participating with product failure analysis collaboratively with project engineers, including the suggestion of product design improvements based on observation and test results.
- Setting up a variety of electrical, mechanical and/or electronic equipment to include environmental chambers, Life Test equipment, Product Specific test equipment, Mechanical gauges and Electrical/Electronic meters.
- Designing and documenting testing configurations and setup. Creating test reports that document test results.
Requirements:
Bachelor's Degree with 0-1 years of experience
Associate's Degree with 1-2 years of experience
Engineering Technician (Medical Device Technology) - Entry/Junior Level (Round Lake)
Posted 1 day ago
Job Viewed
Job Description
Job ID:
We're currently seeking entry/junior level Engineering Technicians who have an interest in the medical device/technology industry. These are all onsite roles (5 days/week) and we're open to either fresh Bachelor graduates with internship experience or those with an Associate's degree and a year of experience working within and engineering lab environment. See below for other details!
Day to Day Responsibilities:
- 50% manual, handling pumps
- 50% taking observations, pull log files of pump (records of what occurred)
- Interacting with a lot of equipment - microscopes, strength and contention testing devices, electrical equipment, etc.
Top Skills Needed:
- Lab experience, collecting data, following procedures (will be trained on documentation practices, lab safety practices, the testing products) but need to be able to read and follow procedures- required
- Writing or developing scripts for electrical mechanical devices- a plus
- Handling electrical mechanical devices, interact with device- a plus
- Softwares: Microsoft, Windows- required (Script, Macro, Programming, Writing preferred)
Responsibilities:
- This position is primarily responsible for the electrical, mechanical, and environmental testing and evaluation of new and existing Electromechanical medical devices. Will be required to handle test stands, set-up, perform and monitor testing activities.
- Testing products in the Reliability Test Lab to test requirements specified by Product and Reliability Engineering.
- Taking direction from the Reliability Test Manager, Lab Supervisor and Test Engineers on safe working procedures, use of equipment, recording of test data, and monitoring of results.
- Performing all tests as directed by the Reliability Test Manager, Lab Supervisor and Test Engineers.
- Providing accurate and timely documented results.
- Communicating test results to appropriate engineering personnel.
- Performing teardown destructive testing or test to failure activities as part of the product development process.
- Verifying and validating proposed and/or implemented changes to existing products. Performing specified tests of competitive products as part of the new product development process.
- Participating with product failure analysis collaboratively with project engineers, including the suggestion of product design improvements based on observation and test results.
- Setting up a variety of electrical, mechanical and/or electronic equipment to include environmental chambers, Life Test equipment, Product Specific test equipment, Mechanical gauges and Electrical/Electronic meters.
- Designing and documenting testing configurations and setup. Creating test reports that document test results.
Requirements:
Bachelor's Degree with 0-1 years of experience
Associate's Degree with 1-2 years of experience
Orthopedic Technologist (Certified Orthopedic Technology or Medical Assistant)
Posted 3 days ago
Job Viewed
Job Description
Midwest Orthopaedics at Rush, with locations in Chicago and the Western Suburbs, is nationally recognized as a leader in comprehensive orthopedic services. The physicians of Midwest Orthopaedics at Rush have received specialized training in orthopedic surgery and in subspecialty areas within the field of orthopedic medicine and can diagnose and treat even the most complicated and rare musculoskeletal conditions. The Orthopedic Program at Rush University Medical Center is ranked Top 10 in the nation by U.S. News and World Report. Midwest Orthopaedics at Rush doctors are the official team physicians for the Chicago White Sox, Chicago Bulls, Chicago Fire Soccer Club and DePaul University Athletics.
Ready to join? We are looking for a full-time Certified Orthopedic Technologist or Medical Assistant to be based at the outpatient clinic in Chicago, IL. The ideal candidate will provide excellent customer service and communication skills. The Orthopedic Technician is responsible for providing assistance to patients and clinical staff in the full scope of orthopedic services. Duties involve casting, splinting, dressing changes, and phlebotomy.
Essential Duties and Responsibilities include the following. Other duties may be assigned.
- Apply and remove and/or assist with casts, splints, and dressings as ordered by the physician.
- As directed by physician, removes staples, sutures and external fixation devices, as well as collects or assists with the collection of specimens, including venipuncture and C&S, and preparing specimens for processing.
- Prepare and fit all types of orthopedic bracing devices and dme.
- Instruct patients regarding care of casts, splints, dressings, dme etc.
- Wound care as directed by physician.
- Adjusts crutches and canes to fit patient.
- Assist front desk with rooming patients in the event it is a slow cast room day.
- Prepares treatment rooms for examination of patients.
- Instructs patients in care of and assists patients in walking with casts, braces, and crutches.
- Ordering supplies and maintaining supply inventory.
- Creating PO for purchasing.
- Ensure rooms are cleaned between patients, as well as cleaned and stocked at the end of the day.
- Travel may be required to any of the 7 MOR clinic locations.
- Other duties as assigned
- High school diploma or general education degree (GED)
- One or more years of orthopedic experience/healthcare experience.
- Certified Orthopedic Technologist
- Certified Medical Assistant
Pay Range: $22.00 - $7.00 per hour. Compensation at MOR is determined by many factors, which may include but are not limited to, job-related skills and level of experience, education, certifications, geographic location, market data and internal equity. Base pay is only a portion of the total rewards package.
- Quarterly Bonus Incentives
- Medical, Dental and Vision Insurance.
- Paid Time Off and Paid Holidays.
- Company-paid life and long-term disability insurance.
- Voluntary life, AD&D, and short-term disability insurance.
- Critical Illness and Accident Insurance.
- 401(k) Savings Plan.
- 401(k) Employer Contribution.
- Pet Insurance.
- Commuter Benefits.
- Employee Assistance Program (EAP).
- Tax-Advantaged Accounts (FSA, HSA, Dependent Care FSA).
- HSA Employer Contribution (when enrolled in a HDHP).
- Tuition Reimbursement.
- Continuing Education of up to 2,500 annualized.
- Excellent working relationship with prestigious group of physicians in Orthopedics in the US and #1 in Illinois and Indiana.
Our employees make the difference in our patients’ lives, and we value their contributions. Midwest Orthopaedics at Rush offers a comprehensive compensation and benefits package and an opportunity to grow and develop your career with an industry leader. Come see what we’re all about. Equal Opportunity Employer.
Equal Opportunity Employer
This employer is required to notify all applicants of their rights pursuant to federal employment laws.
For further information, please review the Know Your Rights notice from the Department of Labor.