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Medical Device Product Development Manager Jobs in Florida

Advanced Medical Supply

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 ...

Advanced Medical Supply

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 ...

Arthrex

Sr. Product Manager, Vet Systems

Naples, FL · On-site

$119K - $157K/yr

Requisition ID: 65189 Title: Sr. Product Manager, Vet Systems Arthrex, Inc. is a global medical device company and a leader in new product development and medical education within the orthopedic ...

ARTHREX

Sr. Product Manager, Vet Systems

Naples, FL · On-site

$119K - $157K/yr

Requisition ID: 65189 Title: Sr. Product Manager, Vet Systems Arthrex, Inc. is a global medical device company and a leader in new product development and medical education within the orthopedic ...

ARTHREX

Product Manager, Vet Systems

Naples, FL · On-site

Product Manager, Vet Systems Arthrex, Inc. is a global medical device company and a leader in new product development and medical education within the orthopedic field. We are actively searching for ...

Arthrex

Product Manager, Vet Systems

Naples, FL · On-site

Product Manager, Vet Systems Arthrex, Inc. is a global medical device company and a leader in new product development and medical education within the orthopedic field. We are actively searching for ...

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Medical Device Product Development Manager information

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 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:

Medical Device Product Development Manager jobs near you
Infographic showing various Medical Device Product Development Manager job openings in Florida 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.

Director, Regulatory Affairs (Product Development)

Arthrex

Naples, FL • On-site

$141K - $186K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 16 days ago

Arthrex rating

7.8

Company rating: 7.8 out of 10

Based on 77 frontline employees who took The Breakroom Quiz

175th of 544 rated manufacturers

Job description

Requisition ID: 66263 Title:Director, Regulatory Affairs (Product Development)
Join Arthrex and help shape the future of medical device innovation.
We are seeking an experienced Director, Regulatory Affairs (Product Development) for our global headquaters in Naples, FL.who will lead regulatory strategy and execution across our product development portfolio, including new product introductions, product modifications, and marketing material approvals. This high-impact leadership role partners closely with Engineering, Product Management, Clinical, Operations, and Quality teams to drive successful product commercialization and global regulatory compliance. At Arthrex, you'll work alongside industry-leading innovators dedicated to improving surgical outcomes worldwide. This is an opportunity to make a significant impact on the development and commercialization of cutting-edge medical technologies while leading a talented regulatory team in a collaborative, mission-driven environment.
Arthrex, Inc. is a global medical device company and a leader in new product development and medical education in orthopedics. Join our talented team at a growing global medical device company focused on Helping Surgeons Treat Their Patients Better™.
Essential Duties and Responsibilities:
  • Lead regulatory oversight for new product development, product design and process modifications, and related engineering changes.
  • Lead a team of Regulatory Affairs people leaders who manage segment-aligned teams and provide regulatory support across the product development lifecycle across all business segments.
  • Serve as the senior regulatory partner to Engineering and Product Management, ensuring early alignment on regulatory strategy and risk mitigation during design and development.
  • Drive integration of regulatory deliverables into design control documentation, technical files, and DHFs.
  • Guide the preparation and strategic planning of regulatory submissions for the U.S. (510(k)), Canada (Medical Device Licenses), and the European Union (CE Marking under MDR).
  • Align regulatory approaches across business segments to ensure consistency in decision-making, risk tolerance, and execution practices.
  • Represent Regulatory Affairs in product development governance, program reviews, and cross-functional working groups.
  • Direct the regulatory review and approval process for promotional and marketing materials related to new and modified products.
  • Support the review and refinement of labeling, instructions for use (IFUs), and promotional claims to ensure compliance with global regulatory standards.
  • Lead regulatory strategy for innovation-focused or high-risk programs in collaboration with internal and external stakeholders.
  • Support the development and performance of regulatory personnel, including leadership coaching and succession planning.
  • Contribute to inspection readiness, regulatory audits, and internal quality system improvement initiatives.

Education and Experience:
  • Bachelor's Degree required; advanced degree preferred (MBA, MS) preferred.
  • 12+ years of experience in Regulatory Affairs with at least 5 years in a leadership role.
  • Demonstrated success managing regulatory personnel and overseeing strategy for product development and change management programs.
  • Knowledge and Skill Requirements/Specialized Courses and/or Training:
  • In-depth knowledge of FDA 510(k) and EU MDR regulatory pathways.
  • Expertise in design control, engineering change processes, risk management, and product lifecycle documentation.
  • Strong leadership, communication, and collaboration skills across cross-functional teams.
  • Ability to translate complex regulatory concepts into actionable strategies for business and technical partners.
  • Ability to plan, evaluate, and improve the efficiency of business processes and procedures to enhance speed, quality, efficiency, and output.
  • Experience in regulatory review of labeling and promotional materials in compliance with FDA, FTC, Health Canada, and EU advertising standards.

Business Impact Statement:
This position plays a critical role in enabling product commercialization by ensuring timely regulatory approvals across the U.S., Canada, and EU. It directly supports revenue generation by protecting product launch timelines and ensuring compliance with evolving global regulatory requirements. The Sr. Director helps safeguard business continuity through regulatory risk mitigation and alignment with internal product development and market release goals.
Autonomy & Decision-Making:
This role operates with significant autonomy in regulatory strategy development, submission planning, and execution oversight. The Sr. Director exercises independent judgment in determining regulatory pathways, assessing risk, managing design control readiness, and driving issue resolution. The individual is accountable for regulatory performance and readiness across multiple product families and global markets, and is empowered to represent the function in high-level cross-functional discussions and business planning.
Language and Communication Skills:
Ability to comprehend and apply language skills to the degree required to perform the job based upon the job requirements listed above. Ability to verbally communicate ideas and issues effectively to other team members and management. Ability to write and record data and information as required by procedures.
Arthrex Benefits
  • Medical, Dental and Vision Insurance
  • Company-Provided Life Insurance
  • Voluntary Life Insurance
  • Flexible Spending Account (FSA)
  • Supplemental Insurance Plans (Accident, Cancer, Hospital, Critical Illness)
  • Matching 401(k) Retirement Plan
  • Annual Bonus
  • Wellness Incentive Program
  • Free Onsite Medical Clinics
  • Free Onsite Lunch
  • Tuition Reimbursement Program
  • Trip of a Lifetime
  • Paid Parental Leave
  • Paid Time Off
  • Volunteer PTO
  • Employee Assistance Provider (EAP)
  • Eligible for discretionary Long Term Incentive program

All qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other status protected by law.
Making People Better at Arthrex
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Job Details
Date: Aug 1, 2026
Requisition ID: 66263
Salary Range:
Job title: Director, Regulatory Affairs (Product Development)
Arthrex
Location:

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