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Director Medical Device Product Development Jobs in Delaware

Danaher

Sales Representative Medical Device

Wilmington, DE · On-site +1

$90K - $100K/yr

... directed by annual performance objectives and quota. This position reports to the Regional Sales ... in a medical device industry preferred * 1+ years capital equipment sales experience preferred ...

IT MINDS L.L.C.

Quality Engineer - Medical Device

Newark, DE · On-site

$70K - $90K/yr

Quality Engineer - Medical Device Location: Delaware Largescale Medical Device client facing a ... Perform detailed reviews of production line documentation, including: o Process documentation o ...

Mary Dickson

Director, Design Assurance

Newark, DE · On-site

$167.40 - $297.60/hr

Direct the Design Assurance organization to support new product development and sustain activities ... Medical Device Directive. * Familiarity with ISO 14970, IEC 60601, IEC 62366, and EN 62304.

Hologic

Senior Software Engineer, Medical Device

Newark, DE · On-site

$119K - $157K/yr

Develop an expert level of understanding of our products and their use in clinical practice, to ... Collaborate with Test Engineers to understand functionality for the development and support of ...

Hologic Inc.

Lead Design Assurance Engineer

Newark, DE · On-site

$119K - $186K/yr

... in medical device development? At Hologic, we are seeking a Lead Design Assurance Engineer to play a pivotal role in new product development, ensuring that design controls, risk management, and ...

Hologic

Lead Design Assurance Engineer

Newark, DE · On-site

$119K - $186K/yr

... in medical device development? At Hologic, we are seeking a Lead Design Assurance Engineer to play a pivotal role in new product development, ensuring that design controls, risk management, and ...

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All JobsMedical Device Product Development JobsDirector Medical Device Product Development JobsDirector Medical Device Product Development Jobs in Delaware

Director Medical Device Product Development information

What is the difference between Director Medical Device Product Development vs Product Manager Medical Devices?

AspectDirector Medical Device Product DevelopmentProduct Manager Medical Devices
ResponsibilitiesOversees entire product development lifecycle, manages teams, sets strategic directionFocuses on product planning, feature definition, and market analysis
Required CredentialsEngineering or life sciences degree, experience in medical device development, regulatory knowledgeBackground in engineering, marketing, or life sciences, familiarity with medical device regulations
Work EnvironmentLeadership role in R&D or product development departments, cross-functional teamsCollaborates with engineering, marketing, and sales teams, often in a more tactical role

The main difference is that the Director Medical Device Product Development leads and manages the entire development process and teams, focusing on strategic oversight, while the Product Manager Medical Devices concentrates on product planning and market needs. The director role involves higher-level management and regulatory oversight, whereas the product manager handles day-to-day product features and customer requirements.

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Director Medical Device Product Development jobs near you

Software Engineer - Medical Device Product Development

Fusion Life Sciences

Newark, DE • On-site

Contractor

Re-posted 4 days ago

Job description

 
Job:Software Engineer – Medical Device Product Development
Location: Newark, DE (Hybrid)
 
Experience: 7+ years
 
Industry Preference: Medical Devices / Regulated Healthcare Products / Embedded or Product Software
Role Summary:
We are seeking a Software Engineer with strong product development experience to support development and maintenance of software systems used in medical device platforms.
The role involves designing, developing, debugging, and maintaining software for both existing and next-generation medical device products, while ensuring compliance with quality and regulatory requirements.The ideal candidate will have experience working in cross-functional engineering environments, supporting the full product software lifecycle from design through
testing and release.
Key Responsibilities:
Product Software Development Design, develop, and maintain software for medical device products and platforms.
Implement new product features and support enhancement of existing systems.
Develop software aligned with product design and system architecture.
Agile Development Work within Agile / Scrum development environments.
Support continuous integration and automated build pipelines.
 
Testing & Debugging
Identify, troubleshoot, and resolve complex software issues.
Support development of software test plans and collaborate with test engineers.
Design Documentation
Create and maintain software requirements, design documentation, and technical specifications.
Ensure documentation supports regulatory and internal compliance requirements.
Cross-Functional Collaboration
Work closely with Design Assurance, Regulatory Affairs, Clinical Affairs, and Quality teams.
Support engineering changes and product improvements.

Product Lifecycle Support
Contribute to development of new products and improvements to existing systems.
Participate in product roadmap discussions and technical design reviews.
Technical Leadership
Provide technical guidance and mentorship to junior engineers.
Support adoption of engineering best practices and quality standards.
Required Qualifications:
5+ years of software development experience in product development environments.
Strong programming skills in C++, C#, .NET, or similar object-oriented languages.
Experience with software architecture, algorithms, and data structures.
Experience debugging and troubleshooting complex systems.
Familiarity with version control systems (Git, SVN, Azure DevOps, etc.).
Strong understanding of software development lifecycle.