Engineering Program Manager
Мэтч & Сопровод
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Описание вакансии
TL;DR
Engineering Program Manager: Planning and directing the design and development of new medical device products or software systems with an accent on technical quality/reliability systems, feasibility studies, and end-to-end documentation through R&D. Focus on coordinating cross-functional and external supplier activities to drive concepts from initial design to market release.
Location: Brooklyn Park, Minnesota, United States of America (Onsite, minimum 4 days a week)
Salary: $142,400 - $213,600 (USD)
Company
is a global healthcare technology company focused on alleviating pain, restoring health, and extending life.
What you will do
- Plan, direct, and implement all aspects of design and development for new medical device products or software systems.
- Develop, evaluate, implement, and maintain technical quality assurance/control and reliability systems and standards.
- Oversee investigation and evaluation of existing technologies and guide conceptualization of new methodologies, materials, machines, processes, or products.
- Direct development of new concepts from initial design through market release, including feasibility studies.
- Monitor documentation maintenance across all R&D phases.
- Coordinate activities with outside suppliers and consultants to ensure timely delivery and select/develop personnel for efficient operations.
Requirements
- Practical experience leading and managing execution of processes, projects, and initiatives within a defined functional area.
- Advanced knowledge and skills in a specific technical or professional discipline.
- Understanding of how work impacts other areas of the organization.
- Bachelor’s degree required (or an equivalent degree meeting U.S. degree requirements for degrees earned outside the United States).
- Minimum 5 years of relevant experience with a bachelor’s degree, or 3 years with an advanced degree.
- Onsite role based in Brooklyn Park, Minnesota (minimum 4 days a week onsite).
Nice to have
- Experience in medical devices or other regulated industries (FDA, ISO 13485, design controls).
- PMP/PgMP or Agile certifications (Scrum, SAFe).
- Experience managing large, complex, or global engineering programs.
- Familiarity with systems engineering, hardware/software integration, or connected devices.
- Experience with program management tools (Jira, Smartsheet, Azure DevOps, MS Project).
- Experience working cross-functionally with R&D, Quality, Regulatory, and Manufacturing teams.
Culture & Benefits
- Competitive salary range and eligibility for a short-term incentive ( Incentive Plan, MIP).
- Health, dental, and vision insurance plus Health Savings Account and Healthcare Flexible Spending Account (for regular employees working 20+ hours/week).
- 401(k) plan with employer contribution and match, paid time off, paid holidays, and employee assistance program.
- Tuition assistance/reimbursement and global well-being program (Simple Steps).
- Onsite collaboration with in-person exchanges as part of the work model.
Hiring process
- Review application profile to confirm minimum requirements are evident.
- Interviews to assess program leadership, technical discipline depth, and cross-functional coordination experience.
- Final evaluation of fit for onsite expectations and role scope.
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