Job Title: Technical Program Manager
Location : Houston, Texas , Minneapolis, Minnesota (Fullty Onsite Role)
Visa : USC, GC, GC EAD, H4 EAD
Notes from the Client:
This would be a "Medical" Technical Program Manager. They are NOT looking for anyone that is outside of the Medical Industry/previous Medical PM.
Companies you can target
Zimmer
Biomet
Cook Medical
Class 3 Medical devices (would be great to have) .."implantable, pacemaker" key words to search.
Position Summary
The Technical Program Manager will manage overall programs of small to medium scope or subsections of larger programs. This role involves leading cross-functional teams to develop and execute strategies for new product development and commercialization of new products. The Program Manager will ensure that programs meet milestones and deliverables, representing thecore team to the organization and external partners, reporting progress, and resolving issues.
Minimum Requirements and Qualifications
Education: BS degree
Experience:
8+ years of experience in end-to-end product implementation within the medical device industry
5+ years of experience leading broad, multi-disciplinary teams
Experience with implantable and connected systems
Managed integration of multiple subsystems as part of a connected medical device program, including cloud/mobile applications/embedded system
Preferred Experience:
Class III medical device product development
Broad, multi-disciplinary technical knowledge in the medical device industry
Experience working in a broader enterprise/cross-functional business environment
Skills:
Strong leadership, organizational, planning, and follow-up skills
Advanced verbal and written communication skills
Ability to work effectively in a team in a fast-paced, changing environment
Ability to work in a highly matrixed and geographically diverse business environment
Ability to synthesize complex business and technical aspects of small to medium-scale development programs
Multi-tasking, prioritizing, and meeting deadlines in a timely manner
Responsibilities
Manage overall programs of small to medium scope or subsections of larger programs
Lead cross-functional teams to develop and execute strategies for new product development and commercialization
Manage resources to ensure programs meet milestones and deliverables
Represent the core team to the organization and external partners
Report team progress, program recommendations, and resolve issues
Develop detailed plans in alignment with strategic objectives, including master schedules, budgets, program milestones, and key tasks and deliverables
Provide guidance and direction to the core team
Identify and assist in clearing barriers to effective progress
Resolve program resource issues and facilitate reallocation of activities and efforts to ensure schedules are achieved
Conduct financial evaluation of programs
Facilitate all core team meetings and track progress against the project plan
Comply with US FDA regulations, other regulatory requirements, company policies, operating procedures, processes, and task assignments
Maintain positive and cooperative communication and collaboration with all levels of employees, customers, contractors, and vendors
Additional Activities
Perform other related duties and responsibilities as assigned
Travel Requirements
This position may require business travel.
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