Product Manager Senior (Science Field)
About The Position
Seize your opportunity to make a personal impact as a Senior Product Manager supporting the Defense Health Agency Operational Medical Systems (OPMED). GDIT is your place to make meaningful contributions to challenging projects and grow a rewarding career. At GDIT, people are our differentiator. Our work depends on a Senior Product Manager utilizing their project management expertise to ensure our client’s medical solutions, including preventive treatments, drugs, diagnostics, hemorrhage control, and battlefield pain management, transition from advanced development and into the hands of the military medical providers on the battlefield.
Requirements
- Bachelor’s degree in Science field
- 8+ years of related experience and at least 5 years in project management
- DoD 5000 Acquisition experience with preparing acquisition documentation for the advance development of medical products
- Not applicable, however must be clearable for a T1 Public Trust
- Exceptional communication, writing, and project management skills for developing documentation and collaborating with diverse teams.
- Adept at cross-functional teamwork and engaging multiple stakeholders.
- Ability to execute using Microsoft Office Suite, Word, PowerPoint, and Excel, as well as Microsoft Outlook
- US Citizenship Required
Nice To Haves
- Master's degree
Responsibilities
- Provide product management support to the assigned medical products
- Lead Integrated Product Teams (IPT), Working Groups (WG), and In-Progress Reviews to include scheduling meetings, facilitating collaboration among all stakeholders, preparing agendas and related documentation, developing meeting minutes, and tracking action items
- Utilize working knowledge of the DoD 5000 acquisition medical product development and PPBE processes to prepare or support the documentation development of Life Cycle Cost Estimates, Single Acquisition Management Plans (SAMP), and Test and Evaluation Master Plans (TEMPs)
- Support the development of integrated master schedules and identify, assess, and mitigate programmatic risks and issues
- Lead all major initiatives to advance product development and associated activities
- Assist with programmatic and technical document review, market research, and vendor site visits/demonstrations
- Support clinical trial protocol development and prepare documentation that complies with the Food and Drug Administration (FDA) requirements
- Independently coordinate, draft and finalize responses for review
- Develop and/or review information papers, acquisition documentation, protocols, etc., when necessary to support assigned products
- Successfully communicate with personnel at various echelons through the use of effective interpersonal and communication skills
- Manage and track numerous, diverse, simultaneous efforts and have the ability to effectively prioritize requirements for multiple on-going projects in support of the product team
- Participate in special projects and other duties as required
Benefits
- AI-powered career tool that identifies career steps and learning opportunities
- An internal mobility team focused on helping you achieve your career goals
- Comprehensive benefits and wellness packages, 401K with company match, and competitive pay and paid time off
- Award-winning culture of innovation and a military-friendly workplace
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
