ZipRecruiter

Log In

1

Medical Device Software Engineer Jobs in New York

Clarapath Inc

Embedded Software Engineer

Hawthorne, NY · On-site

$115K - $155K/yr

Embedded Software Engineer LOCATION: Hawthorne, NY (on-site) TYPE : Full time, regular COMPENSATION ... We are looking for a team player who views medical device development as a competitive advantage.

Clarapath Inc

Embedded Software Engineer

Hawthorne, NY

$115K - $155K/yr

Embedded Software Engineer LOCATION: Hawthorne, NY (on-site) TYPE : Full time, regular COMPENSATION ... We are looking for a team player who views medical device development as a competitive advantage.

Clarapath

Embedded Software Engineer

Hawthorne, NY · On-site

$138K - $182K/yr

We are looking for a Software Engineer who will assist in the development of our next generation ... Develop software for medical device within a well-established robotics framework. * Driver ...

Clarapath

Embedded Software Engineer

Hawthorne, NY

$138K - $182K/yr

We are looking for a Software Engineer who will assist in the development of our next generation ... Develop software for medical device within a well-established robotics framework. * Driver ...

Jj

Principal Med Device Security Engineer

Raritan, NJ · On-site +1

... performing medical device company. This is an exciting opportunity to impact development ... Ability to generate SBOMs from Software source code and Binaries, Firmware, and Operating Systems

Danaher

Software Engineer Internships

Flushing, NY

Producing documentation to support medical device regulatory processes Who This Is For * Students graduating in 2026 or later with a Bachelor's degree in Computer Science, Software Engineering ...

Danaher

Software Engineer Internships

Stamford, CT

Producing documentation to support medical device regulatory processes Who This Is For * Students graduating in 2026 or later with a Bachelor's degree in Computer Science, Software Engineering ...

next page

Showing results 1-20

All JobsMedical Device Software Engineer JobsMedical Device Software Engineer Jobs in New York

Medical Device Software Engineer information

See New York salary details

$69.5K

$161.4K

$224.8K

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

As of Aug 6, 2026, the average yearly pay for medical device software engineer in New York is $161,396.00, according to ZipRecruiter salary data. Most workers in this role earn between $131,300.00 and $189,300.00 per year, depending on experience, location, and employer.

How do you become a medical device software engineer?

To become a medical device software engineer, individuals typically need a bachelor's degree in software engineering, computer science, or a related field. Experience with embedded systems, programming languages like C or C++, and knowledge of medical device regulations such as FDA standards are important. Certifications in quality management or regulatory compliance can also enhance job prospects.

What are the key skills and qualifications needed to thrive as a medical device software engineer?

To thrive as a Medical Device Software Engineer, you need a solid background in software development, embedded systems, and biomedical engineering, often supported by a degree in computer science, electrical engineering, or a related field. Experience with programming languages like C/C++, knowledge of real-time operating systems, and familiarity with medical device regulatory standards such as IEC 62304 are typically required. Strong problem-solving skills, attention to detail, and effective communication are essential soft skills for this position. These skills ensure high-quality, compliant software that contributes to safe and reliable medical devices, which are critical for patient health.

What is a medical device software engineer?

A Medical Device Software Engineer is responsible for designing, developing, testing, and maintaining software used in medical devices. They ensure compliance with regulatory standards like FDA and IEC 62304 while working on embedded systems, user interfaces, or cloud-based healthcare applications. Their role involves collaborating with cross-functional teams, including hardware engineers and regulatory specialists, to ensure patient safety and product effectiveness.

What are the typical daily responsibilities of a medical device software engineer?

Medical Device Software Engineers typically spend their days designing, coding, and testing software for medical devices in compliance with health regulations. They collaborate closely with hardware engineers, quality assurance teams, and regulatory specialists to ensure that the software integrates seamlessly with device hardware and meets performance and safety standards. Documenting development processes, participating in code reviews, and addressing feedback from cross-functional teams are also common aspects of the role. This position often requires troubleshooting issues in both simulated and real clinical environments to ensure the reliability and safety of the device.

What are the most commonly searched types of Medical Device Software Engineer jobs in New York? The most popular types of Medical Device Software Engineer jobs in New York are:
What are popular job titles related to Medical Device Software Engineer jobs in New York? For Medical Device Software Engineer jobs in New York, the most frequently searched job titles are:
What job categories do people searching Medical Device Software Engineer jobs in New York look for? The top searched job categories for Medical Device Software Engineer jobs in New York are:
Medical Device Software Engineer jobs near you
Infographic showing various Medical Device Software Engineer job openings in New York as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 15% Part Time, and 6% Contract. Highlights an 91% Physical, 1% Hybrid, and 8% Remote job distribution, with an average salary of $161,396 per year, or $77.6 per hour.

Design Software Quality Consultant (Medical Devices)

Stark Pharma Solutions Inc

Piscataway, NJ • Remote

Contractor

Re-posted 6 days ago

Job description

Hi,

My name is Karthik Mutyala, from Stark Pharma Solutions Inc, we are hiring talents for our client. I am working on Design Software Quality position right now. Please send me your updated resume if you have relevant experience and interested in this position. The detailed job description is as follows

Role: Design Software Quality Consultant (Medical Devices)

Location: REMOTE
Duration: Long Term
 

Position Overview

We are seeking an experienced Design Software Quality Consultant to support post-acquisition integration activities for a medical device product portfolio. This role will focus on ensuring software design quality, regulatory compliance, and successful integration of acquired products into the client's quality management system.

The ideal candidate will have deep expertise in Software Design Quality, Model-Based Systems Engineering (MBSE), and medical device software compliance, with experience supporting new product development in regulated environments.

Key Responsibilities

  • Review and assess Design History Files (DHFs) and product development documentation for acquired medical device products.
  • Support software design quality activities during post-acquisition product integration.
  • Ensure compliance with internal quality standards and global regulatory requirements.
  • Lead Model-Based Systems Engineering (MBSE) activities for software-enabled medical devices.
  • Review software engineering deliverables to ensure compliance with design controls and quality requirements.
  • Partner with cross-functional teams including R&D, Software Engineering, Quality, and Regulatory Affairs.
  • Support risk management, usability engineering, and software lifecycle compliance activities.

Required Qualifications

  • 10+ years of Software Quality Engineering experience in the medical device industry.
  • Strong experience with Software Design Quality and Design Controls.
  • Hands-on experience with Model-Based Systems Engineering (MBSE).
  • Experience supporting software quality for new product development or medical device integration/remediation projects.
  • Knowledge of IEC 62304, IEC 60601, ISO 14971, and medical device software regulations.
  • Experience with Software as a Medical Device (SaMD).
  • Strong understanding of software verification, validation, and compliance within regulated environments.

I am actively connecting with professionals for current and upcoming opportunities. If you are open to exploring new roles or would like to stay informed about relevant positions, please send me your updated resume along with the best number and time to reach you.  

Please follow Stark Pharma Solutions on LinkedIn for the latest job updates: https://www.linkedin.com/company/99455976/

Thank you,

Karthik Mutyala

Recruiting Manager

Stark Pharma Solutions Inc

Email: karthik@starkpharma.com

15 Corporate Place S, Suite 350,

Piscataway, New Jersey 08854

www.starkpharma.com