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Medical Device Product Development Manager Jobs (NOW HIRING)

Norsk Titanium

Product Development Manager

Plattsburgh, NY · On-site

$107K - $125K/yr

Norsk Titanium is hiring a Product Development Manager for our Plattsburgh, NY additive manufacturing site!Who is Norsk Titanium? What do we do? If you haven't heard our name in passing before, you ...

SharkNinja

Product Development Manager

Needham, MA · On-site

$124K - $155K/yr

Manager, Product Development -- Shark Robots Needham, MA (onsite) At SharkNinja, Product ... medical insurance, dental insurance, vision insurance, flexible spending accounts, health savings ...

SharkNinja

Product Development Manager

Needham, MA · On-site

$124K - $155K/yr

... new product development (creation and management) of assigned product(s) from brainstorm phase ... medical insurance, dental insurance, vision insurance, flexible spending accounts, health savings ...

HIS LLC

PRODUCT DEVELOPMENT MANAGER

Manhattan, NY · On-site

$126K - $157K/yr

Product Manager JOB OVERVIEW Revision Date- 10/2021 * Understand and execute HIS International/account product initiatives of assigned programs from fabric sourcing through style development up until ...

Cosmo Appliances

Product Development Manager

Chino, CA · On-site

$23 - $28/hr

Review and test product samples to evaluate new developments and market fit. * Analyze product defects, generate detailed reports, and provide actionable insights to management for quality ...

Itron, Inc

Product Development Manager

West Union, SC · Hybrid

$96K - $121K/yr

The Product Development Manager at our Oconee, SC manufacturing facility leads a multidisciplinary engineering team to design and deliver innovative electro-mechanical solutions for the Utilities and ...

DS2

Product Development Manager

Niceville, FL · On-site

$120K - $155K/yr

DS2 is seeking a Product Development Manager to lead innovative software development teams in building the next generation of aerospace mission planning capabilities. In this role, you will ...

WELLMEI MOLD

Be Seen First

Market Development Manager - Injection Mold/Injection Molding

Abbott Park, IL · Remote

$80K - $120K/yr (+ commission)

Develop new business opportunities with North American healthcare and medical device manufacturers ... Familiarity with supplier sourcing, new product development (NPI), or tooling procurement processes.

SharkNinja

Product Development Manager

Needham, MA · On-site

$124K - $155K/yr

... new product development (creation and management) of assigned product(s) from brainstorm phase ... medical insurance, dental insurance, vision insurance, flexible spending accounts, health savings ...

SharkNinja

Product Development Manager

Needham, MA · On-site

$124K - $155K/yr

... new product development (creation and management) of assigned product(s) from brainstorm phase ... medical insurance, dental insurance, vision insurance, flexible spending accounts, health savings ...

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Medical Device Product Development Manager information

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$42.5K

$127K

$144.5K

How much do medical device product development manager jobs pay per year?

As of Sep 5, 2026, the average yearly pay for medical device product development manager in the United States is $126,987.00, according to ZipRecruiter salary data. Most workers in this role earn between $114,500.00 and $143,000.00 per year, depending on experience, location, and employer.

What does a medical device product development manager do?

A Medical Device Product Development Manager oversees the entire process of bringing a medical device from the concept stage to market launch. They coordinate cross-functional teams, manage timelines, ensure compliance with regulatory standards, and oversee testing and validation of products. Their responsibilities also include working with engineers, designers, and regulatory specialists to ensure the device meets safety, efficacy, and user needs. Ultimately, they play a critical role in ensuring that new medical devices are developed efficiently, safely, and in compliance with industry standards.

How does a medical device product development manager typically collaborate with cross-functional teams during the development process?

A Medical Device Product Development Manager works closely with cross-functional teams, including engineering, regulatory affairs, quality assurance, marketing, and clinical experts, to ensure that product requirements are met throughout each development phase. They facilitate regular meetings to align on project milestones, address potential risks, and incorporate feedback from various stakeholders. This collaborative environment helps ensure that the final product complies with regulatory standards and meets market needs, making strong communication and project management skills essential in this role.

What are the key skills and qualifications needed to thrive as a medical device product development manager, and why are they important?

To thrive as a Medical Device Product Development Manager, you need expertise in engineering or life sciences, experience with product lifecycle management, and knowledge of regulatory requirements, often supported by a relevant degree. Familiarity with CAD software, project management tools, and compliance systems such as ISO 13485 or FDA regulations is typically required. Strong leadership, cross-functional communication, and problem-solving skills help drive innovation and align diverse teams. These competencies are vital to ensure products are developed efficiently, safely, and in compliance with industry standards.

What is the difference between Medical Device Product Development Manager vs Medical Device Quality Assurance Specialist?

AspectMedical Device Product Development ManagerMedical Device Quality Assurance Specialist
CredentialsEngineering degree, certifications like PMP or PDMAQuality assurance certifications like CQE, ISO auditor
Work EnvironmentDesign teams, R&D, cross-functional project groupsQuality labs, compliance departments, manufacturing oversight
Industry UsageLeading product development from concept to launchEnsuring products meet quality and regulatory standards

The Medical Device Product Development Manager focuses on designing and developing new medical devices, managing cross-functional teams, and bringing products to market. In contrast, the Medical Device Quality Assurance Specialist ensures that products meet quality standards and regulatory requirements throughout the development and manufacturing process. Both roles are essential in the medical device industry but serve different functions in product lifecycle management.

What is medical device product development?

Medical device product development involves designing, testing, and bringing new medical devices to market, ensuring they meet safety and regulatory standards. A Medical Device Product Development Manager oversees this process, coordinating cross-functional teams, managing timelines, and ensuring compliance with industry regulations such as FDA or ISO standards.

What cities are hiring for Medical Device Product Development Manager jobs?

Cities with the most Medical Device Product Development Manager job openings:

What are the most commonly searched types of Medical Device Product Development jobs?

The most popular types of Medical Device Product Development jobs are:

What states have the most Medical Device Product Development Manager jobs?

States with the most job openings for Medical Device Product Development Manager jobs include:

Medical Device Product Development Manager jobs near you
Infographic showing various Medical Device Product Development Manager job openings in the United States 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 $126,987 per year, or $61.1 per hour.

Senior Software Engineer - Medical Device (Onsite - Irvine, CA) Possible Temp-to-Hire

Pharmavise

Irvine, CA • On-site

$130K - $172K/yr

Contractor

Re-posted 21 days ago

Job description


Our F500 Medical Device client has an exciting opportunity for a Senior Software Engineer.
Job Summary:
We are seeking a skilled Senior Software Engineer to join the Client's Urology team. In this role, you will be responsible for technical activities related to the customization and validation of the Android Operating System (version 5) deployed within a Class III medical device. This role bridges software engineering, cybersecurity, and medical device product integration for a commercial product. The successful candidate will assess, modify, and harden the Android OS to close cybersecurity gaps, adapt critical applications for compatibility, and perform OS-level verification and validation in alignment with regulated product development standards.
This role will work closely with cybersecurity, systems, and quality engineers to ensure system integrity, compliance, and reliable performance of the Android-based platform within the medical device system.
Responsibilities:
• Analyze and modify Android OS (v5) source to address identified cybersecurity vulnerabilities and compliance gaps.
• Implement OS-level patches, configuration changes, and security controls consistent with medical device cybersecurity guidance (FDA premarket & post market cybersecurity, and EU MDCG ).
• Manage integration of third-party libraries and drivers while maintaining software traceability and regulatory documentation.
• Adapt and refactor existing applications to ensure compatibility with the custom Android OS as needed.
• Optimize interprocess communication, resource management, and hardware interface behaviors in the updated OS environment.
• Collaborate with application developers to test and validate functionality per intended use.
• Conduct OS-level verification and validation per IEC 62304 and internal design control SOPs
• Support risk analysis and mitigation activities per ISO 14971 and internal software QMS SOPs.
• Contribute to software documentation, including software architecture, verification plans, test protocols, and traceability matrices.
• Participate in technical reviews and audits to ensure software compliance with applicable standards.
• Work in close coordination with cybersecurity, software, design quality, and system engineering teams to ensure secure and reliable system operation.
• Support integration testing and root cause analysis of OS-related issues.
Job Requirements:
• Bachelor's or master's degree in computer engineering, computer science, electrical engineering, or a related field.
• 7+ years of professional software engineering experience, with at least 3 years in Android OS development or customization.
• Hands-on experience with AOSP, Android build systems, and kernel-level modification.
• Strong understanding of embedded systems, Linux internals, and Android application frameworks.
• Proven experience in regulated environments (medical device, aerospace, automotive, or defense).
• Working knowledge of IEC 62304, ISO 14971, IEC 60601, and other regulations.
• Familiarity with cybersecurity risk assessment, threat modeling, and vulnerability remediation in embedded platforms.
Preferred Qualifications
• Experience with Android OS version 5 or legacy Android platforms in long-lifecycle products.
• Strong debugging, profiling, and reverse-engineering skills.
• Prior experience supporting device certification and regulatory submissions.
• Excellent communication and documentation skills for technical and compliance deliverables.
Other Details:
• Schedule: 08:00:AM - 04:30:PM
• Contract Length: 12 Months with possible extension
• Work Set-Up: Hybrid in Arbor Lakes, MN
• Start Date: 1/5/2026

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