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Medical Device Product Development Manager Jobs in Missouri

United Rentals

Product Development Manager

Saint Louis, MO · On-site

$110K - $138K/yr

As a Product Development Manager (PDM) within its Advanced Solutions Group (ASG), you will be focused on driving innovation and maturing ASG's offering portfolio by piloting, enhancing and preparing ...

United Rentals

Product Development Manager

Branch, MO · On-site

$104K - $130K/yr

As a Product Development Manager (PDM) within its Advanced Solutions Group (ASG), you will be focused on driving innovation and maturing ASG's offering portfolio by piloting, enhancing and preparing ...

Jobtailor

Staff Design Quality Engineer

California, MO · On-site

$90 - $130/hr

* Support new hardware and software medical device product development * Support sustaining product ... Interact with R&D, Program Management, Manufacturing Operations and Engineering, Quality Management ...

DeepSight Technology

Program Manager

Saint Louis, MO · On-site

$120K - $180K/yr

The ideal candidate will have experience managing product development programs within the medical device industry. Responsibilities * Drive complex product programs from initial concept/definition ...

DeepSight Technology

Program Manager

Saint Louis, MO · On-site

$120K - $180K/yr

The ideal candidate will have experience managing product development programs within the medical device industry.Responsibilities Drive complex product programs from initial concept/definition ...

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All JobsMedical Device Product Development JobsMedical Device Product Development Manager JobsMedical Device Product Development Manager Jobs in Missouri

Medical Device Product Development Manager information

See Missouri salary details

$35.7K

$113.9K

$130.2K

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

As of Aug 23, 2026, the average yearly pay for medical device product development manager in Missouri is $113,901.00, according to ZipRecruiter salary data. Most workers in this role earn between $103,100.00 and $129,300.00 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 are the most commonly searched types of Medical Device Product Development jobs in Missouri?

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

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

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

Medical Device Product Development Manager jobs near you
Infographic showing various Medical Device Product Development Manager job openings in Missouri 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 $113,901 per year, or $54.8 per hour.

Senior Compliance Engineer - Digital Health, Connected Medical Devices

Jobtailor

Portage Des Sioux, MO • On-site

$95 - $140/hr

Other

Posted 5 days ago

Job description

Responsibilities
  • Provide dedicated compliance engineering support for Stryker Medical’s Smart Care portfolio of software as/in a Medical Device, hardware, sensors, and customer applications
  • Lead product compliance strategy for new product development and sustaining engineering activities
  • Translate global regulatory and compliance requirements into design inputs, verification plans, and market access strategies
  • Drive compliance activities from concept development through verification, validation, and commercialization
  • Assess compliance risks, predicate product considerations, and emerging requirements
  • Integrate compliance requirements into system architecture, product design, and technology roadmaps
  • Define compliance test strategies, methods, operating environments, and worst-case conditions
  • Manage external testing laboratories, certification bodies, and third-party partners for global certifications and regulatory submissions
  • Serve as a technical compliance subject matter expert during design reviews, risk assessments, and development activities
  • Support procedure development, technical reviews, innovation opportunities, and cross-business initiatives
  • Collaborate with stakeholders and business units to align compliance strategies with user needs, product classifications, and market requirements
Requirements
  • Bachelor’s degree in Computer Science, Software Engineering, Electrical Engineering, or related discipline
  • 4+ years of compliance engineering experience required
  • Experience with product safety regulatory certification for major standards bodies and frameworks, including IEC 60601-1, IEC 60601-1-8, FCC Requirements, and IEC 62368-1
  • Experience with medical device product development lifecycle, including design controls and risk management
  • Experience working with and managing third-party certification laboratories such as UL, TÜV, CSA, and Intertek
  • Experience with device regulatory certification involving safety, EMC, and/or wireless standards
  • Knowledge of telecom/non-medical device standards
  • Familiarity with different software development life cycles
  • Basic knowledge of regulatory certification and device submission processes
  • Ability to work independently and effectively in a matrixed organization
  • Ability to work cross-functionally with Research & Development, Regulatory Affairs, and Marketing
  • Strong written, verbal, and interpersonal communication skills with the ability to influence without authority
Core Competencies

Demonstrates expertise in compliance engineering for medical devices, including regulatory certification processes and product safety standards. Proficient in managing compliance activities throughout the product development lifecycle while collaborating cross-functionally to align strategies with market requirements.

Highest-signal resume keywords
  • Compliance Engineering Experience
  • Regulatory Certification Knowledge
  • Product Safety Standards Expertise
  • Medical Device Development Lifecycle
  • Cross-Functional Collaboration
ATS Optimization Keywords Hard Skills
  • Compliance Engineering
  • Regulatory Certification
  • Risk Management
  • Design Controls
  • IEC 60601-1
  • IEC 60601-1-8
  • FCC Requirements
  • IEC 62368-1
  • Device Submission Processes
  • Telecom Standards
Soft Skills
  • Strong Communication Skills
  • Influencing Without Authority
  • Independent Work
  • Cross-Functional Teamwork
Industry Keywords
  • Medical Device
  • Compliance Strategy
  • Product Development
  • Verification Plans
  • Market Access Strategies
Tools & Technologies
  • Third-Party Certification Laboratories
  • UL
  • TÜV
  • CSA
  • Intertek
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