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Sr. Program Manager - Medical Device
Resolution MedicalUnited Statesfull_timeVerifiedPosted 27 Mar 2024
About the role
Description
Job Summary
The Sr Program Manager is responsible for the successful planning, management and execution of complex, usually multi-device product development projects and all applicable standard operating procedures. The Sr Program Manager will lead a cross-functional team consisting of product development, quality, manufacturing, and procurement personnel, through the Product Development cycle from concept to commercialization, as defined by customer development agreements.
Essential Functions
- Manage a portfolio of complex initiatives that span one or multiple lines of business
- Provide on-site leadership for project team by building and motivating team members to meet project goals, adhering to their responsibilities and project milestones
- Full project life cycle ownership: successful project delivery will include meeting or exceeding customer expectations with respect to project deliverables
- Report on project success criteria results, metrics, test and deployment management activities
- Work creatively and analytically within Resolution Medical’s problem-solving environment demonstrating teamwork, innovation and excellence
- Participate in establishing practices, templates, policies, tools and partnerships to expand and mature these capabilities for the organization
- Support preparation of estimates and develop detailed project plans for all phases of the project
- Procure adequate resources to achieve project objectives in planned timeframes
- Provide status reporting regarding project milestones, deliverable, dependencies, risks and issues, communicating across leadership
- Demonstrate a functional acumen to support how solutions will address customer goals while maintaining alignment with Resolution Medical and industry best practices
- Manage project scope and changes
- Manage ongoing quality control and participate in quality issue resolution
- Define the Statement of Work and Specifications for the requested goods and services
- Develop and manage all aspects of project and program engagement from planning, external vendor relationships, communications, resources, budget, change, risks and issues
- Provide progress reports as requested by key stakeholders
- Coach, mentor, motivate and supervise project team
- Ensure that projects and programs are proceeding according to scope, schedule, budget and quality standards
- Support continued development of best practices, templates, policies, tools and partnerships to expand and mature these capabilities for the organization
- Support company finance, accounting, human resources, and quality as necessary to ensure compliance with requirements
Requirements
Education, Experience, Required Skills
- Minimum of a Bachelor level degree in a Scientific or Technical Field and 15+ years or more experience in regulated industry, such as Pharmaceuticals or Medical Devices
- Minimum of 10 years Project Management experience within a Regulated Industry such as Pharmaceuticals or Medical Devices.
- Ability to handle and be trusted with confidential and/or sensitive information
- Able to work in a fast-paced, constantly changing environment
- Ability to be flexible and to handle multiple projects in an organized, timely manner
- Able to problem-solve, work under pressure, and to effectively manage stress
Physical Requirements
- Prolonged periods of sitting at a desk and working on a computer
- Must be able to lift up to 25 pounds at times
- Must have excellent hand-eye coordination
- Ability to differentiate between colored wires, tabs, and electronic components preferred
- Must wear gown, gloves, ear protection and other personal protective equipment as applicable
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