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Medical Device Embedded Software Engineer Jobs in Collierville, TN

Tegra Medical

Quality Engineer

Hernando, MS · On-site

$67K - $87K/yr

The role of the Quality Engineer is to assist in the planning, executing, and finalizing projects ... software in the medical device or related industry. * Experience with ISO 13485:2016 standard and ...

Osv_bioventus

Sr Quality Engineer

Memphis, TN · On-site

$86K - $116K/yr

... and/or software. Electrical Engineering or related fields preferred. * Minimum 5 years (with Bachelor's) or 4 years (with Master's) of experience within the medical device industry with a ...

Osv_bioventus

Sr Quality Engineer

Memphis, TN · On-site

$86K - $116K/yr

... and/or software. Electrical Engineering or related fields preferred. * Minimum 5 years (with Bachelor's) or 4 years (with Master's) of experience within the medical device industry with a ...

Bioventus

Sr Quality Engineer

Memphis, TN · On-site

$86K - $116K/yr

... and/or software. Electrical Engineering or related fields preferred. * Minimum 5 years (with Bachelor's) or 4 years (with Master's) of experience within the medical device industry with a ...

CONMED

Design Quality Engineer II

Memphis, TN · On-site

A relentless focus on the safety and the efficacy of the medical device. * Review and approve engineering designs/changes for adequate quality, reliability, maintainability, risk management, modeling ...

Integra LifeSciences

Project Engineer II

Cordova, TN · On-site

Minimum of 3 years of industry experience in engineering; medical device industry experience is a ... Software: familiarity with CAD (i.e. solidworks) and statistical analysis (i.e. minitab). PHYSICAL ...

Integra LifeSciences

Project Engineer II

Cordova, TN · On-site

Minimum of 3 years of industry experience in engineering; medical device industry experience is a ... Software: familiarity with CAD (i.e. solidworks) and statistical analysis (i.e. minitab). PHYSICAL ...

Cisco

Software Engineer, Backend

Memphis, TN · On-site

$155K - $222K/yr

... the software development lifecycle. Preferred Qualifications * Programming experience in Rust ... S. employees are offered benefits, subject to Cisco's plan eligibility rules, which include medical ...

Cisco

Senior Software Engineer, Backend

Memphis, TN · On-site +1

$165K - $241K/yr

... the software development lifecycle. Preferred Qualifications * Programming experience in Rust ... S. employees are offered benefits, subject to Cisco's plan eligibility rules, which include medical ...

Osv_bioventus

Sr Sustaining Engineer

Memphis, TN · Hybrid

$88K - $109K/yr

... embedded systems. * Hands-on experience with root cause analysis, engineering testing, design of ... Experience working within medical device quality systems, manufacturing controls, complaint ...

Osv_bioventus

Sr Sustaining Engineer

Memphis, TN · Hybrid

$88K - $109K/yr

... embedded systems. * Hands-on experience with root cause analysis, engineering testing, design of ... Experience working within medical device quality systems, manufacturing controls, complaint ...

Bioventus

Sr Sustaining Engineer

Memphis, TN · On-site

$88K - $109K/yr

... embedded systems. * Hands-on experience with root cause analysis, engineering testing, design of ... Experience working within medical device quality systems, manufacturing controls, complaint ...

Globus Medical

Quality Engineer

Memphis, TN · On-site

$69K - $90K/yr

... medical device regulations and ISO 13485 quality system requirements. As a contributor to the quality engineering organization, this professional will be a self-motivated and characterized as an ...

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Showing results 21-40

All JobsMedical Device Embedded Software Engineer JobsMedical Device Embedded Software Engineer Jobs in Collierville, TN

Medical Device Embedded Software Engineer information

See Collierville, TN salary details

$61.9K

$135.6K

$153.9K

How much do medical device embedded software engineer jobs pay per year?

As of Aug 6, 2026, the average yearly pay for medical device embedded software engineer in Collierville, TN is $135,647.00, according to ZipRecruiter salary data. Most workers in this role earn between $116,300.00 and $153,000.00 per year, depending on experience, location, and employer.

What is a medical device embedded software engineer?

Medical Device Embedded Software Engineers are professionals who design, develop, and maintain the specialized software that runs on hardware inside medical devices, such as pacemakers, infusion pumps, and imaging machines. They ensure that the software meets strict regulatory standards for safety, reliability, and performance. Their work involves programming, testing, debugging, and documenting embedded code, as well as collaborating with hardware engineers and regulatory teams to bring safe and effective medical products to market.

What is the difference between Medical Device Embedded Software Engineer vs Firmware Engineer?

AspectMedical Device Embedded Software EngineerFirmware Engineer
CredentialsBachelor's in Electrical, Computer Engineering, or related; often certifications in medical device standardsBachelor's in Electrical, Computer Engineering, or related; certifications vary by industry
Work EnvironmentMedical device companies, regulated environments, quality assurance focusConsumer electronics, industrial, or embedded systems companies
Industry UsagePrimarily in healthcare, medical device manufacturingBroader tech sectors, including consumer electronics and industrial systems
Search & Comparison IntentHigh overlap in embedded systems, safety standards, and certification requirements

The Medical Device Embedded Software Engineer and Firmware Engineer roles share core skills in embedded systems development. However, the Medical Device Embedded Software Engineer focuses specifically on medical device safety, regulatory compliance, and working within healthcare environments. Firmware Engineers may work across various industries without the strict medical standards, making the Medical Device Embedded Software Engineer role more specialized in healthcare applications.

What are the key skills and qualifications needed to thrive as a medical device embedded software engineer, and why are they important?

To thrive as a Medical Device Embedded Software Engineer, you need a strong background in embedded systems design, C/C++ programming, and a degree in electrical engineering, computer engineering, or a related field. Familiarity with real-time operating systems (RTOS), hardware-software integration, and industry standards like IEC 62304 or FDA regulations is typically required. Attention to detail, strong problem-solving abilities, and effective teamwork are vital soft skills for this role. These competencies are crucial for developing reliable, safe, and compliant software that meets stringent healthcare requirements.

What are some common challenges faced by medical device embedded software engineers when working on cross-functional teams?

Medical Device Embedded Software Engineers often collaborate closely with hardware engineers, regulatory specialists, and quality assurance teams. A common challenge is ensuring that software requirements align with hardware limitations and regulatory standards, which can necessitate frequent adjustments and clear documentation. Additionally, balancing the pace of software development with the rigorous testing and validation processes required for medical devices can be demanding. Effective communication and adaptability are essential to navigate these multidisciplinary interactions and deliver safe, compliant products.
What cities near Collierville, TN are hiring for Medical Device Embedded Software Engineer jobs? Cities near Collierville, TN with the most Medical Device Embedded Software Engineer job openings:
Medical Device Embedded Software Engineer jobs near you

6Q02 - Quality - QAEN - QUALITY ASSURANCE ENGINEER

Inteplast Group, Ltd

Gallaway, TN • On-site

Full-time

Re-posted 2 days ago

Job description

TITLE: Quality Assurance Engineer
POSITION OBJECTIVE: Assists the Quality Assurance and Regulatory Affairs Manager in regulatory compliant company-wide quality assurance department that provides all research, support, product development, and quality assurance functions required along with accurate specifications, service, and delivery of product to our customers. Assist the Quality Assurance and Regulatory Affairs Manager in the management of the quality assurance department to support production schedules, personnel, resources and continuous improvement efforts that achieve efficient service productivity. Assists the Quality Assurance and Regulatory Affairs Manager in the evaluation and controls to vendor reliability of goods and services.
QUALIFICATIONS:
  • To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
  • Bachelor's degree in industrial engineering, mechanical engineering, or business from an accredited four-year college is preferred. Associate's degree or equivalent from an accredited two-year college/technical school, or higher will be considered, plus 2-4 years of quality assurance engineering experience in a medical device manufacturing environment; or equivalent combination of education and experience. Experience in Plastic Injection and/or Blow Molding is desired.
  • Must have working knowledge of the FDA 21 CFR Part 820 Quality System Regulation.
  • Working knowledge of ISO 13485:2016 Standard is preferred.
  • Current certified ISO 13485:2016 Lead Auditor certificate is preferred.
  • Computer literate in Microsoft Office suite and experience with imputing data into database systems is a must. Proficiency in SAP is a plus.
  • Ability to apply common sense understanding to carry out detailed written or oral instructions. Ability to deal with problems involving concrete variables in standardized situations.
  • Ensure consistent, dependable attendance and demonstrate a willingness to accommodate non-standard work hours as necessary.
  • Capable of effectively managing job-related stress and fostering productive workplace interactions.

JOB RESPONSIBILITIES:
  • Assists the Quality Assurance and Regulatory Affairs Manager in developing and maintaining a complete, comprehensive, and compliant quality management system that supports the manufacture and sourcing of medical products in FDA product device classes I and II and Health Canada Class I; currently excluding FDA Device Class III and Health Canada Device Class II, III, IV products.
  • Assists the Quality Assurance and Regulatory Manager with medical device company compliance to various regulatory agencies and regulations; specifically, the FDA and Health Canada: QSR and applicable cGMP's, AMMI Sterilization Standards, OSHA, EPA and other federal, state and local regulatory agencies.
  • Assists Quality Assurance and Regulatory Affairs Manager in the compliance and maintenance of the quality management system.
  • Provides the quality engineering function assuring that products meet their intended use through product specification, continuous evaluation, and data analysis.
  • Provides the company-wide training in statistical techniques and quality science.
  • Directs technical and administrative personnel engaged in quality assurance activities.
  • Evaluates and provides for audits, corrective actions, preventive actions, and compliance verification of internal and external quality management systems and their functions.
  • Investigates, prepares, and maintains records for customer complaints with root cause analysis along with corrective action, preventive action, and effectiveness check.
  • Acts as a quality representative for customers and vendors.
  • Assures validation and compliance of our medical device products through our contract sterilization facilities and our sourced medical device products sterilization facilities.
  • Acts as a quality representative for customers and vendors.
  • Other duties as assigned by Quality Assurance and Regulatory Affairs Manager.

WORK ENVIRONMENT CONDITIONS SUBJECTED TO IN THIS POSITION:
  • Office environment consists of a fixed or modular office that includes adequate lighting, heating/cooling, equipment and furniture in a good working condition.
  • Must be able to work constructively and cheerfully in an environment that may be stressful due to adversarial situations, and at all times maintaining company as well as employee confidentiality.
  • Must be able to tolerate a manufacturing environment of noise, fumes, and particulates generated from various types of plastic materials and equipment.

Inteplast Group is an Affirmative Action and Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.
If you need a reasonable accommodation for any part of the employment process, please contact us by email at applicantaccommodation@inteplast.com and let us know the nature of your request and your contact information. Requests for accommodation will be considered on a case-by-case basis. Please note that only inquiries concerning a request for reasonable accommodation will be responded to from this email address.
For more information, about our commitment to equal employment opportunity, view the EEO - Know Your Rights and Pay Transparency Statement.

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