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Medical Device Product Development Manager Jobs (NOW HIRING)

Abbott

Product Development Engineer

Santa Clara, CA · On-site

Plan, develop, and execute design verification activities for medical device systems and subsystems ... Support risk management activities through verification of risk control measures and investigation ...

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Medical Device Product Development Manager information

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$42.5K

$127K

$144.5K

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

As of Jul 21, 2026, the average yearly pay for medical device product development manager in the United States is $126,987.00, according to ZipRecruiter salary data. Most workers in this role earn between $114,500.00 and $143,000.00 per year, depending on experience, location, and employer.

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 cities are hiring for Medical Device Product Development Manager jobs? Cities with the most Medical Device Product Development Manager job openings:
What are the most commonly searched types of Medical Device Product Development jobs? The most popular types of Medical Device Product Development jobs are:
What states have the most Medical Device Product Development Manager jobs? States with the most job openings for Medical Device Product Development Manager jobs include:
Medical Device Product Development Manager jobs near you
Infographic showing various Medical Device Product Development Manager job openings in the United States as of July 2026, with employment types broken down into 1% As Needed, 83% Full Time, 14% Part Time, and 2% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $126,987 per year, or $61.1 per hour.

Business Development Consultant For Medical Device Manufacturer

MedCepts

Bowling Green, KY • On-site

Full-time

Re-posted 18 days ago

Job description

Description
We are a manufacturer looking for manufacturers reps and consultants for business development throughout North America. ISO 13485:2003, 9001:2008, FDA Compliant. Seeking sales rep or consultants to call on engineers, product development, senior buyers at medical device mfgrs such as Biomet, Edwards LifeSciences, J&J, or to other CNC shops as secondary source to fill overflow capacity. Opportunities also exist to create new products for surgeons. Little customer service or follow up required. We are looking for opportunities to quote and will pay 8% if quotes become manufacturing product.
REGULATORY COMPLIANCE ISO, FDA CERTIFICATIONS
• ISO 13485:2003
• ISO 9001:2008
Since 1996
Woman owned
100% Made in America
BUSINESS CAPABILITIES OVERVIEW
Our company's Engineering has a substantial amount of experience with medical device product development, technology development, project management and manufacturing. Our inhouse design and manufacturing of complex precision machined components and final product assembly meets customers development and production needs. We can manage a project through the entire project life cycle-from prototype through full-scale production. Our founder was also a Co-Founder of Symbiosis Corporation (Founded in 1985) a leader and pioneer in the emergence of disposable medical instruments. Symbiosis introduced disposable instruments in two areas of treatment: Low-cost biopsy forceps that were marketed through Microvasive, a subsidiary of Boston Scientific Corporation, and Laparoscopic instruments that were marketed through Ethicon Endosurgery, a Johnson & Johnson subsidiary.
PROJECT MANAGEMENT
When a project is entered into the Manufacturing data base, an engineer/project leader is selected to manage and implement a project from concept/customer design specifications through commercialization to the customer. The project leader remains accountable for each project through the project or product life cycle. Project leaders are responsible for design for manufacturing and target pricing.
TECHNOLOGY DEVELOPMENT
We have a substantial amount of experience with enabling technology development for multiple medical device specialties.
PRODUCT DEVELOPMENT
It all starts with a customer's 3D model from a 3D modeling program such as Solid Works or ProEngineer. Our company converts the customer's product geometry into CNC machine code utilizing various computer automated manufacturing software programs. Customer prototypes are quickly produced through a fully staffed tool-room, and rapid printing and prototyping systems. Engineers generate CNC programs, design manufacturing tooling and quickly integrate new manufacturing processes into selected production centers. Measurement systems and test methods are also developed to ensure first article inspection dimensions and specifications requirements are met.
MANUFACTURING
Manufacturing methods and equipment are designed in-house with a special emphasis placed on Lean manufacturing and Six Sigma methodologies. Equipment is designed for standardization, and modular set-up. Engineers and machine operators participate in the design, programming and set-up of 5-axis CNC Milling, Swiss CNC Turning, CNC Multi-Axis Grinding and secondary processing operations. Our company utilizes Lean Design andManufacturing methodologies, and determines the most efficient and cost-effective methods of manufacturing.
CONTRACT MANUFACTURING
Long-term manufacturing agreements enable year-over-year savings for our customers. These savings are achieved through continuous improvement, and year-over-year efficiency gains.
MEDICAL DEVICE PRODUCT EXPERIENCE
• Endoscopy Biopsy Forceps
• Endoscopy Surgical Devices
• Laparoscopic Electrosurgical Devices
• Cardiovascular Devices
• Stent Delivery Systems (Balloon expandable and self-expanding Nitinol stent delivery systems)
• Stent Manufacturing
• Guidewire Manufacturing
• Cardiovascular Biotomes
• Artherectomy Devices
• Cardiac Surgery Instrumentation
• Ventricular Assist Devices
• Rhythm Management and Defibrillation Devices
• Abdominal Aortic Aneurysm (AAA) Devices
• Endovascular Devices
• Neurovascular Devices
• Orthopaedic Trauma Products
• Orthopaedic Plate and Screw Systems
• Small and Large Bone Plate and Screw Systems
• Intramedullary Fixation Devices
• Dental Implants
PRODUCT DEVELOPMENT AND MANUFACTURING CAPABILITIES:
• 3D Modeling
• Rapid Prototyping and 3D Printing
• Investment Casting
• Swiss CNC Turning
• CNC-3-5 Axis Milling
• CNC 8-Axis Grinding
• EDM and Wire EDM
• Titanium Anodizing
• Laser Marking
• Laser, TIG and MIG Welding
• Electropolishing
• Metal Polishing and Finishing
• Heat Treatment of Metals
• Micro-Bead Blasting
• Passivation
• Bending and Forming
• Clean Room Assembly
• Manufacturing Documentation
• Manufacturing Scale-up
• Design and Product Transfer to Customers
• Test Method Development and Validation
• Product and Process Validation
• Lean Manufacturing
• Six Sigma Methodologies
Candidate Profile: At least 10 years experience selling to or working with medical device manufacturers of all sizes including start ups looking for engineering and prototype work. Relationships with surgeons and device r&d labs extremely helpful.
Training required: Marketing collateral and in-house technical experts. No technical expertise required on your part, just open the door for us. We are looking for someone to generate leads, open doors, use their contacts to get us to the right people, and we'll take it from there.

Apply