1

Medical Device Risk Management Jobs in Nebraska (NOW HIRING)

Performs data management, scheduling, documentation, education and other duties associated with ... Completion of post-high school course work in medical or related field desired. OTHER CREDENTIALS ...

Performs data management, scheduling, documentation, education and other duties associated with ... Completion of post-high school course work in medical or related field desired. OTHER CREDENTIALS ...

Therapy Manager (Sales Rep)

Omaha, NE · On-site

$85K - $255K/yr

Mainstay Medical Mainstay Medical is a medical device company focused on marketing an innovative ... Territory Management & Growth * Analyze market trends, referral patterns, and territory ...

Our customers include more than 40 of the top 50 medical device companies and eight of the top ten ... Experience managing and supporting enterprise network environments, including LAN/WAN and wireless ...

... in Med Device or Life Sciences organizations. * Strong facilitation skills with proven ability to ... Curious and innovative, with the ability to push boundaries while navigating governance and risk.

The ideal candidate has a proven track record in medical device sales, is highly strategic, goal ... Account & Territory Management * Build and maintain a robust sales pipeline using Salesforce.com to ...

The ideal candidate has a proven track record in medical device sales, is highly strategic, goal ... Account & Territory Management * Build and maintain a robust sales pipeline using Salesforce.com to ...

... M system. * Drive lead generation activities through continuous review and refinement of ... Minimum 5 years of medical device industry experience selling physician preference therapies in the ...

Quality Engineer

Holdrege, NE · On-site

$86K - $111K/yr

Overview emBecta is a global medical device company with a 100‑year legacy in insulin delivery ... SUMMARY As directed by the Quality Engineering Manager, the Quality Engineer II is accountable for ...

Consistently use Salesforce.com to manage sales funnelopportunitydevelopment and at-risk business ... Experience in Medical Device products, both capital and disposable, for specific surgery procedures ...

embecta is a global medical device company with a 100-year legacy in insulin delivery and diabetes ... Support and influence change management within the plant: liaison between the core team, program ...

embecta is a global medical device company with a 100-year legacy in insulin delivery and diabetes ... Support and influence change management within the plant: liaison between the core team, program ...

Investigator

Elkhorn, NE · On-site

$40 - $60/hr

Ethos Risk Services is a leading insurance claims investigation and medical management company ... A handheld camcorder with high-quality zoom and a covert camera device. Use of stabilization ...

Showing results 41-60

Medical Device Risk Management information

What is medical device risk management?

Medical device risk management is the systematic process of identifying, evaluating, and controlling risks associated with medical devices throughout their lifecycle. This process ensures that potential hazards are minimized to protect patient safety and comply with regulatory standards, such as ISO 14971. Risk management includes activities like risk assessment, implementing controls, monitoring, and documenting all steps to demonstrate compliance. It is a critical function in the design, manufacturing, and post-market phases of medical device development.

How does a medical device risk management professional typically collaborate with cross-functional teams during the product development lifecycle?

Medical Device Risk Management professionals work closely with engineering, regulatory affairs, quality assurance, and clinical teams to identify, assess, and mitigate potential risks associated with medical devices. They participate in design reviews, facilitate risk assessments such as FMEA, and ensure that risk controls are effectively implemented and documented according to regulatory standards like ISO 14971. Regular communication and collaboration are essential to align risk management activities with project timelines and compliance requirements, ensuring patient safety and product success.

What are the key skills and qualifications needed to thrive in medical device risk management, and why are they important?

To thrive in Medical Device Risk Management, you need a solid background in engineering or life sciences, a thorough understanding of regulatory standards (such as ISO 14971), and experience in risk assessment processes. Familiarity with risk management software, quality management systems, and relevant regulatory databases is typically required, along with certifications like Certified Risk Manager (CRM) or RAC. Strong analytical thinking, attention to detail, and effective communication are crucial soft skills for evaluating risks and collaborating with cross-functional teams. These competencies ensure the safety and compliance of medical devices, protecting both end-users and the company from regulatory or safety issues.

What is the difference between Medical Device Risk Management vs Medical Device Quality Assurance?

AspectMedical Device Risk ManagementMedical Device Quality Assurance
Primary FocusIdentifying, evaluating, and mitigating risks associated with medical devicesEnsuring products meet quality standards and regulatory requirements
CertificationsISO 14971, RAPS certifications often preferredISO 13485, regulatory compliance certifications
Work EnvironmentDesign and development teams, risk analysis meetingsManufacturing, inspection, and quality control departments
Industry UsageUsed throughout product lifecycle for safety managementUsed to maintain product quality and compliance

While both roles are essential in the medical device industry, Risk Management focuses on minimizing safety risks throughout the product lifecycle, whereas Quality Assurance ensures products consistently meet quality and regulatory standards. Understanding these differences helps professionals align their skills with industry needs.

What job categories do people searching Medical Device Risk Management jobs in Nebraska look for?

The top searched job categories for Medical Device Risk Management jobs in Nebraska are:

What cities in Nebraska are hiring for Medical Device Risk Management jobs?

Cities in Nebraska with the most Medical Device Risk Management job openings:

Infographic showing various Medical Device Risk Management job openings in Nebraska as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 17% Part Time, and 5% Contract. Highlights an 91% Physical, 1% Hybrid, and 8% Remote job distribution.

Cardiac Device Specialist

Lincoln, NE • Remote

Bryan Health
Health Care and Social Assistance • 5 - 10K employees

Full-time

This job post has expired today. Applications are no longer accepted.


Bryan Health rating

6.9

Company rating: 6.9 out of 10

Based on 123 frontline employees who took The Breakroom Quiz


Job description

GENERAL SUMMARY: 

Responsible for the programming of arrhythmic devices in a safe and effective manner.  Troubleshoots and determines device solutions, conducts in-clinic and remote monitoring. Performs data management, scheduling, documentation, education and other duties associated with Arrhythmia Services.   

PRINCIPAL JOB FUNCTIONS: 

  1. *Commits to the mission, vision, beliefs and consistently demonstrates our core values. 

  1. *Performs and evaluates in-clinic and remote monitoring, including analyzing rhythm strips for proper device function. 

  1. *Operates a variety of programmers (Biotronik, Boston Scientific, ELA, Medtronic, and Abbott) to assess pacemaker, defibrillator and implantable loop monitor function during clinic visits. 

  1. *Attaches ECG electrodes to patients, as necessary, to assist in achieving proper documentation of sensing and capture during programming as well as other troubleshooting issues; maintains patient comfort and safety during procedures. 

  1. *Evaluates symptoms prior to physician evaluation to gather data on chronotropic incompetence, when symptoms occur; correlates to device function as needed. 

  1. *Analyzes and provides solutions to remote technical problems related to transmission quality and transmitter function. 

  1. *Analyzes and provides solutions to programming technical problems related to quality of ECG and programmer function. 

  1. *Provides technical support to physicians, patients and other staff as needed.   

  1. *Researches device issues related to generators, lead wires, adapters, programming choices and helps summarize data/information for midlevel, cardiologist or electrophysiologist.  

  1. *Contacts appropriate personnel/vendor when a device problem is identified and needs follow-up. 

  1. *Enters implant data, programming changes, appointments and other information, as needed, in current database system. 

  1. *Ensures that charges and diagnoses are documented and submitted to Billing Services via Electronic Health Record (EHR) for arrhythmic devices and procedures. 

  1. Schedules remote, pacemaker and Implantable Cardiac Device (ICD), and implantable loop recorder. 

  1. Contacts nursing homes, physicians, outstate cardiology clinic sites and other people, as necessary, to schedule appointments; reschedule appointments and send out appointment letters as needed. 

  1. *Creates remote and clinic reports for pacemakers, ICDs and implantable loop recorders, generated from current database. 

  1. *Records interactions with patients in progress notes of EHR when necessary; provides information to office nurses when further physician follow-up is needed. 

  1. Educates healthcare professionals, patients and others on various aspects of pacing and defibrillation. 

  1. *Teaches patients and family members how to properly operate remote transmitters; reinforces concepts and information provided to patients and their families by physician, mid-levels and other staff. 

  1. *Participates in continuing education to meet requirements of cardiac device specialist certification; endeavors to keep abreast of new and developing technologies associated with the area of pacing and electrophysiology. 

  1. *Assists physicians and staff in complying with end-of-life decisions, helping educate and arrange programming to deactivate devices as needed. 

  1. Assists in developing procedures to maintain efficiency in the department, office, outstate clinics and other areas within Bryan Heart. 

  1. Maintains professional growth and development through seminars, workshops, and professional affiliations to keep abreast of latest trends in field of expertise. 

  1. Participates in meetings, committees and department projects as assigned. 

  1. Performs other related projects and duties as assigned.  

EDUCATION AND EXPERIENCE: 

High school diploma or equivalency required.  Completion of post-high school course work in medical or related field desired.   

OTHER CREDENTIALS / CERTIFICATIONS: 

Basic Life Support (CPR) certification required. Bryan Health recognizes American Heart Association (for healthcare 

professionals), American Red Cross (for healthcare professionals) and the Military Training Network. 

International Board of Heart Rhythm Education Certified Cardiac Device Specialist (IBHRE CCDS) encouraged but not required after five (5) years of employment.  


What Bryan Health employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom