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Medical Device Product Development Manager Jobs in Ohio

Vesco Medical

Product Development Engineer

New Albany, OH · On-site

... management system are required. Primary Responsibilities * Lead assigned medical-device projects ... At least three years of product-development engineering experience in the medical-device industry.

Posted today

UFP Industries

Product Development Manager

Blanchester, OH · On-site

$101K - $127K/yr

Job Summary We are seeking an experienced and highly motivated Senior Industrial Designer / Product Development Manage with 5-7 years of experience leading product development and innovation ...

Westfield

Product Development Manager

Westfield Center, OH · On-site

$116K - $145K/yr

Job Summary The Product Development Manager is responsible for the ongoing maintenance, development, and delivery of Insurance product offerings. The role oversees and is accountable for the product ...

Westfield

Product Development Manager

Westfield Center, OH · Hybrid

$100K - $126K/yr

Job Summary The Product Development Manager is responsible for the ongoing maintenance, development, and delivery of Insurance product offerings. The role oversees and is accountable for the product ...

Bridgestone

Product Development Manager

Brook Park, OH · On-site

$107K - $134K/yr

As we expand our portfolio, we are seeking a Product Development Manager to lead the creation and launch of next-generation credit card products. This role is key to driving innovation ...

Belcan

Electrical Engineer

Cincinnati, OH

$50 - $60/hr

Familiarity with regulated medical device development, design controls, risk management inputs ... constrained product architectures. * Experience integrating motors, actuators, sensors, power ...

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

Medical Device Product Development Manager information

See Ohio salary details

$37K

$117.9K

$134.8K

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

As of Aug 31, 2026, the average yearly pay for medical device product development manager in Ohio is $117,853.00, according to ZipRecruiter salary data. Most workers in this role earn between $106,700.00 and $133,800.00 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 Ohio?

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

Medical Device Product Development Manager jobs near you

Lead Medical Device Product Lifecycle Engineer

KK Associates

Blue Ash, OH • On-site

$66K - $85K/yr

Other

Re-posted 21 hours ago

Job description

Job Title: Senior Medical Device Quality & Validation Engineer
Location: Blue Ash, OH
Duration: 6 months
Role Descriptions: 7+ years of engineering experience in medical device or other regulated industries. Experience leading cross-functional technical projects. Experience with component development, supplier qualification, design verification, and manufacturing validation. Strong understanding of design controls, change management, risk management, process validation, and quality system compliance.
Must Have Technical/Functional Skills
Strong expertise in Medical Device Product Lifecycle Management (PLM), Design Controls, and Engineering Change Management (ECO/ECN/ECR).
Hands-on experience with Design Verification & Validation (V&V), test methods, protocol development, and technical documentation.
Deep understanding of Risk Management methodologies, including ISO 14971, DFMEA, PFMEA, and hazard analysis.
Knowledge of Quality Management Systems (QMS), ISO 13485, FDA 21 CFR Part 820/QMSR, and regulatory compliance requirements.
Experience in Supplier Quality Engineering, component qualification, supplier development, and Design for Manufacturability (DFM). Proficiency in Process Validation activities including IQ/OQ/PQ, pilot builds, validation builds, and manufacturing transfer. Ability to interpret engineering drawings, GD&T, tolerance stack-ups, specifications, and acceptance criteria. Strong root cause analysis and problem-solving skills utilizing 8D, CAPA, 5 Why, Fishbone, and corrective action processes. Excellent project management skills, including planning, scheduling, risk management, stakeholder management, and cross-functional coordination. Effective leadership, communication, and influencing skills, with the ability to drive decisions and deliver results without direct authority.
Roles & Responsibilities
Lead multiple high-priority lifecycle change projects from concept through implementation.
Drive project plans, timelines, risk mitigation strategies, and implementation readiness.
Coordinate cross-functional teams across Engineering, Quality, Regulatory, Manufacturing, Supply Chain, Procurement, Operations, and external suppliers.
Serve as the technical interface with suppliers for component development, DFM reviews, tooling readiness, process capability, and component qualification.
Support design verification and validation activities, including test planning, execution, data review, and technical documentation.
Partner with manufacturing sites on process validation activities, including IQ/OQ/PQ, pilot builds, validation builds, and production launch readiness.
Apply strong knowledge of design controls, engineering change management, risk management, quality system requirements, and regulatory expectations.
Review engineering drawings, specifications, GD&T requirements, tolerance analyses, and component acceptance criteria.
Drive root cause analysis, technical problem solving, and timely closure of project issues.
Communicate project status, risks, decisions, and recommendations clearly to stakeholders and senior leadership.
Demonstrate strong ownership, urgency, accountability, and ability to influence without direct authority.

Generic Managerial Skills, If any
Strong communication skills, with proficiency in reading, writing, and speaking English.
Ability to multitask, understand customer requirements, and respond promptly and accurately.
Capability to prioritize and manage multiple tasks in a fast paced environment.
Ability to understand and follow complex written procedures.
Ability to work effectively in a team environment and contribute to team goals.
Strong decision making and problem solving abilities with sound situational judgment.
Essential Skills: EIS : MDD Risk Management
Desirable Skills:
Keyword:
Skills: EIS : New Product Development (NPD) Methodology and Management~EIS : MDD Risk Management
Experience Required: 6-8

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