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Medical Device Product Development Manager Jobs in Florida

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Product Development Manager - Medical Device

Pompano Beach, FL · On-site

$107K - $134K/yr

The primary role of the Product Development Manager is to plan, organize and direct engineers to ... Minimum 5+ years of engineering experience within the medical device industry. * 3+ years in a ...

New

Medical Device Rep

Boca Raton, FL · On-site

$82K - $113K/yr

... development and promotion of medical supplies and device products. We believe that our proven ... Ability to effectively manage a physician-based customer base * Skills to communicate clinically ...

Medical Device Rep

Sarasota, FL · On-site

$82K - $113K/yr

... development and promotion of medical supplies and device products. We believe that our proven ... Ability to effectively manage a physician-based customer base * Skills to communicate clinically ...

Product Development Manager

Cape Canaveral, FL · On-site

$97K - $121K/yr

Job Summary The Product Development Manager guides and manages the lifecycle of new technology offerings as well as feature enhancements to the company's product portfolio. This is an onsite position ...

... medical device company and a leader in new product development and medical education in orthopedics and cardiothoracic surgery. Arthrex is actively searching for a Product Manager or a Sr. Product ...

Medical Device Sales Rep

Tampa, FL · On-site

$84K - $114K/yr

Promote and sell products to current and potential customers within a defined geography. * Develop ... Understand and execute sales territory management and customer development. * Establish and ...

... medical device company and a leader in new product development and medical education in orthopedics and cardiothoracic surgery. Arthrex is actively searching for a Product Manager or a Sr. Product ...

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Medical Device Product Development Manager information

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.

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 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 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.
What are the most commonly searched types of Medical Device Product Development jobs in Florida? The most popular types of Medical Device Product Development jobs in Florida are:
What cities in Florida are hiring for Medical Device Product Development Manager jobs? Cities in Florida with the most Medical Device Product Development Manager job openings:
Infographic showing various Medical Device Product Development Manager job openings in Florida as of July 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution.

Product Development Manager - Medical Device

Medical Device Manufacturing Co

Pompano Beach, FL • On-site

$107K - $134K/yr

Full-time

Medical, Dental, Vision, Life, PTO

Posted 3 days ago

New

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Job description

Departmental Manager providing direct management of engineers, supervisors, and technicians. Allocates resources based upon departmental plans & budgets. Responsible for hire/fire decisions within their department. Submits departmental budgets, performance / productivity targets and reports on results. Measured against performance plan goals and objectives.


The primary role of the Product Development Manager is to plan, organize and direct engineers to meet company objectives for design, development of new products and make improvements to existing products by performing the following duties personally or through subordinates. This manager ensures that all engineering activities are completed on time and conform to the standards as established by design control procedures.


Duties and Responsibilities:

• Supervise the team of engineers within the product development department.

• Responsible for the development of new products as determined by the company’s product development roadmap. Continually researches for new methods or components to enhance or improve existing products.

• Prepare and/or review engineering change requests; coordinate cross functional teams to determine feasibility, develop and oversee preparation and implementation of all engineering change notices and document change control.

• Responsible for maintaining and implementing processes and procedures covered by design control.

• Assist quality and compliance in the implementation of the quality system including but not limited to support in conducting risk analysis, closing customer complaints, CARs, internal audits, and other activities covered by the quality system.

• Assist manufacturing operations with development of processes, tooling, molds, and design transfer necessary to produce new products.

• Provide customer service and sales & marketing departments with orientation and training on new products, and assist with preparation of sales presentations, service/repair methods, and marketing literature.

• Perform other duties as assigned.


Required Qualifications:

• Bachelor’s degree in mechanical engineering.

• Minimum 5+ years of engineering experience within the medical device industry.

• 3+ years in a leadership role within product development, engineering, design, etc.

• Experience with GMP and other regulatory compliance requirements.

• Experience with design & development of medical devices within a design control process.

• Prior hands-on customer interaction and proven experience understanding the voice of the customer.

• Change management: willing to make hard fact-based decisions, comfortable with anuninstructed and changing environment.

• Skilled at developing new ideas from both a product and process perspective.

• Demonstrated practical application of design FMEA, value engineering, and design for manufacturability concepts.

• Extensive experience in 3D CAD modeling and 2D dimensioning using Solidworks.


Physical / Mental Demands:

• Working conditions are normal for an office environment.

• Work may require weekend and evening work.

• Work may require travel.

• Physical activity includes sitting, walking, standing, bending, squatting, reaching above shoulders and lifting up to 40 pounds.

• Work under stress in a fast-paced environment.

• Must be alert, able to concentrate, and use good judgment.


Company Description

IMI specializes in tamper-evident technologies that help prevent drug diversion and misuse. Our solutions are essential to hospital and pharmacy drug security programs.