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Medical Device Program Manager Jobs in Ohio (NOW HIRING)

L3HHCM20

Program Manager

Cincinnati, OH · Hybrid

... Device, and Height of Burst Sensor development and manufacturing for DoD weapon systems. We are ... The Program Manager will typically spend their time; 80% on development of new or manufacturing of ...

L3Harris Technologies

Program Manager

Cincinnati, OH · Hybrid

... Device, and Height of Burst Sensor development and manufacturing for DoD weapon systems. We are ... medical conditions), gender identity, gender expression, sexual orientation, marital status ...

NAMSA

Client Success Program Manager

Northwood, OH · On-site

$75K/yr

... to focus solely on medical device materials for safety. NAMSA started testing medical devices ... Program/project management experience preferred PMP and CAPM certification preferred. Working ...

Venteon

Program Manager

Cincinnati, OH · On-site

Medical / Dental / Vision * 401(k) Responsibilities of the Program Manager * Serve as the primary point of contact for assigned aerospace customer programs from award through production and delivery

Venteon

Program Manager

Cincinnati, OH · On-site

Medical / Dental / Vision * 401(k) Responsibilities of the Program Manager * Serve as the primary point of contact for assigned aerospace customer programs from award through production and delivery

L3Harris Technologies

Program Manager

Mason, OH · On-site

Program Manager Job Code: 42085 Job Location: Mason, OH Job Schedule: 9/80: Employees work 9 out of ... medical conditions), gender identity, gender expression, sexual orientation, marital status ...

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All JobsMedical Device Program JobsMedical Device Program Manager JobsMedical Device Program Manager Jobs in Ohio

Medical Device Program Manager information

See Ohio salary details

$36.6K

$102.2K

$149.3K

How much do medical device program manager jobs pay per year?

As of Aug 6, 2026, the average yearly pay for medical device program manager in Ohio is $102,162.00, according to ZipRecruiter salary data. Most workers in this role earn between $75,600.00 and $126,000.00 per year, depending on experience, location, and employer.

What is the difference between Medical Device Program Manager vs Medical Device Quality Engineer?

AspectMedical Device Program ManagerMedical Device Quality Engineer
CredentialsProject management certifications, engineering degreeQuality assurance certifications (e.g., CQE), engineering degree
Work EnvironmentCross-functional teams, project planning, product developmentQuality systems, compliance, testing, and validation
Employer & Industry UsageMedical device companies, manufacturing, R&DRegulatory agencies, manufacturing, quality departments
Search & Comparison IntentManaging projects, product launches, timelinesEnsuring quality, compliance, risk management

The Medical Device Program Manager focuses on overseeing product development projects, coordinating teams, and ensuring timely delivery. In contrast, the Medical Device Quality Engineer concentrates on maintaining quality standards, regulatory compliance, and testing processes. Both roles are essential in the medical device industry but serve different functions within the product lifecycle.

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

To thrive as a Medical Device Program Manager, you need a strong background in project management, regulatory compliance, and biomedical engineering or a related field, often supported by a relevant degree and industry experience. Familiarity with project management tools (such as MS Project), quality management systems (QMS), and certifications like PMP or Six Sigma are highly valued. Exceptional leadership, cross-functional communication, and problem-solving skills help drive successful product development and team coordination. These competencies ensure programs meet regulatory standards, stay on schedule, and deliver safe, effective medical devices to market.

What is a medical device program manager?

A Medical Device Program Manager oversees the planning, development, and execution of projects related to medical devices within a company. They coordinate cross-functional teams, manage timelines, ensure regulatory compliance, and serve as the main point of contact for stakeholders. Their role is crucial in bringing safe and effective medical devices from concept to market, ensuring that all aspects of the program meet quality and regulatory standards. Medical Device Program Managers often work closely with engineering, quality assurance, regulatory affairs, and marketing teams.

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

A Medical Device Program Manager works closely with cross-functional teams including engineering, regulatory affairs, quality assurance, manufacturing, and marketing throughout the product development lifecycle. They coordinate timelines, facilitate communication, and resolve conflicts to ensure project milestones are met while maintaining compliance with regulatory standards. Regular meetings and progress updates are essential, as the Program Manager acts as a central point of contact to align various team goals and address issues proactively. This collaborative approach helps streamline development and supports successful product launches.
What are popular job titles related to Medical Device Program Manager jobs in Ohio? For Medical Device Program Manager jobs in Ohio, the most frequently searched job titles are:
What job categories do people searching Medical Device Program Manager jobs in Ohio look for? The top searched job categories for Medical Device Program Manager jobs in Ohio are:
What cities in Ohio are hiring for Medical Device Program Manager jobs? Cities in Ohio with the most Medical Device Program Manager job openings:
Medical Device Program Manager jobs near you
Infographic showing various Medical Device Program Manager job openings in Ohio 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 $102,162 per year, or $49.1 per hour.

Lead Medical Device Product Lifecycle Engineer

KK Associates

Blue Ash, OH • On-site

$66K - $85K/yr

Other

Posted 6 days 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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