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Program Manager (Medical Device)
- LCI-Lawinger Consulting (Fridley, MN)
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Job Summary
The Program Manager is responsible for planning, managing, and executing complex, multi-device product development projects in alignment with applicable standard operating procedures. This role leads cross-functional teams—including product development, quality, manufacturing, and procurement—from concept through commercialization as defined by customer agreements.
Essential Functions
+ Manage a portfolio of complex projects spanning one or multiple business lines.
+ Provide on-site leadership, motivating teams to meet goals, responsibilities, and milestones.
+ Own full project life cycle; ensure delivery meets or exceeds customer expectations.
+ Track and report on project metrics, milestones, testing, and deployment activities.
+ Work collaboratively and analytically to support a high-performance, solutions-focused environment.
+ Contribute to the development of organizational practices, templates, policies, tools, and partnerships.
+ Support project estimation and develop detailed plans for all project phases.
+ Secure and manage resources necessary to meet project objectives and timelines.
+ Communicate project status, milestones, risks, and issues to leadership.
+ Understand and align solutions with customer goals and industry best practices.
+ Manage scope, change control, and project documentation.
+ Oversee ongoing quality control and support resolution of quality issues.
+ Define Statements of Work and product/service specifications.
+ Manage all aspects of project and program engagement, including planning, vendor relationships, communication, budgeting, change management, risk, and issue tracking.
+ Provide progress updates to stakeholders.
+ Coach, mentor, and supervise project team members.
+ Ensure adherence to scope, schedule, budget, and quality standards.
+ Support internal functions such as finance, accounting, HR, and quality to ensure compliance.
Requirements
Education & Experience
+ Bachelor’s degree in a scientific or technical field; 10+ years of experience in a regulated industry (e.g., pharmaceuticals or medical devices).
+ Minimum 10 years of project management experience in a regulated environment.
Skills & Competencies
+ Ability to manage confidential and sensitive information.
+ Comfortable in a fast-paced, dynamic environment.
+ Strong organizational skills; able to manage multiple projects simultaneously.
+ Effective under pressure with strong problem-solving abilities.
Compensation: $110k-$155k + Bonus
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