Project (Design) Mgr 3

Overview

On Site
$111 - $111
Contract - W2

Skills

Agile
Budget
Collaboration
Communication
Computer Hardware
Computer Science
Confluence
Continuous Improvement
Cross-functional Team
Development Testing
Documentation
Human Factors And Ergonomics
ISO 13485
ISO 9000
JIRA
Leadership
Management
Medical Devices
Organizational Skills
PMP
Process Improvement
Product Management
Project Management
Project Planning
Quality Assurance
Robotics
Software Development
Software Development Methodology
Stakeholder Engagement
Regulatory Compliance
Reporting
Requirements Elicitation
Resource Management
System Integration
System Requirements
Waterfall
Workflow

Job Details

Position Summary:

We are seeking a dynamic and experienced Software Project Manager to lead and coordinate the development of cutting-edge surgical robotic platforms. The successful candidate will be responsible for managing software development lifecycles, ensuring timely delivery, compliance with medical device standards, and collaboration across multidisciplinary teams including but not limited to: product management, software & controls engineers, hardware engineers, clinical design engineers, human factors, regulatory and quality engineering teams.

Key Responsibilities:

Manage Full Software Development Lifecycle:

Plan, track, and oversee software project activities from requirements gathering to design, development, testing, validation, documentation, and release.

Cross-Functional Team Leadership:

Facilitate communication and collaboration among inter-, and intra-project teams (with several cross-functional stakeholders) to ensure project success.

Project Planning & Tracking:

Develop detailed project schedules, set milestones, allocate resources, monitor progress, and proactively mitigate risks. Provide clear communication to the organization on accurate project status, critical path, as well as potential areas of risk

Stakeholder Engagement:

Serve as the main point of contact for project stakeholders, reporting on project status, challenges, and solutions.

Regulatory Compliance:

Support the team to ensure deliverables adhere to regulatory standards (e.g., IEC 62304, ISO 13485, FDA 21 CFR Part 820), documentation, and quality system requirements.

Continuous Improvement:

Explore process improvements and arrive at recommendations for future adoption relevant to best practices in agile, waterfall, or hybrid project management methodologies tailored to medical device software.

Budget & Resource Management:

Track project budgets, forecasts, and resources to keep projects on target.

Qualifications:

Bachelor s or Master s degree in Computer Science, Engineering, or related technical discipline.

5+ years of project management experience in software development, with at least 2-3 years in medical device or robotics.

Proven track record leading software projects for medical devices, preferably surgical robotics.

Solid understanding of software development methodologies (Agile, Waterfall, Hybrid).

Familiarity with surgical robotic platforms, control software, integration with hardware systems, and surgical workflow.

Strong knowledge of regulatory requirements for medical software (IEC 62304, ISO 14971, FDA regulations).

Exceptional communication, leadership, and organizational skills.

Project Management Professional (PMP) or equivalent certification preferred.

Experience with project management tools (JIRA, MS Project, Confluence, etc.).

Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.