Senior Project Manager - 246300 Job at Medix™, Maple Grove, MN

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  • Medix™
  • Maple Grove, MN

Job Description

Senior Project Manager – Medical Device Development

About the Role

An established medical device solutions provider is seeking a Senior Project Manager to lead cross-functional initiatives that bring innovative products from concept through commercialization. This position is ideal for a strategic, detail-oriented leader who thrives in a fast-paced, regulated environment and enjoys guiding complex projects from idea to market launch.

Key Responsibilities

  • Lead multi-disciplinary teams to execute new product development projects within scope, schedule, and budget.
  • Develop and maintain detailed project plans, resource forecasts, budgets, and risk management strategies.
  • Serve as the primary liaison between internal teams, clients, and external partners—driving alignment, transparency, and accountability.
  • Ensure all deliverables meet regulatory requirements and internal quality standards.
  • Proactively identify project risks and implement mitigation strategies to protect timelines and deliverables.
  • Facilitate collaboration and communication across engineering, manufacturing, quality, and business development functions.
  • Conduct project reviews and apply lessons learned to strengthen future execution.
  • Contribute to business development efforts through feasibility assessments and project scoping.
  • Mentor junior project managers and foster a culture of operational excellence.

Qualifications

  • Bachelor’s degree in Engineering, Business, or related field (Master’s preferred).
  • 5+ years of project management experience within the medical device or highly regulated manufacturing industry.
  • Demonstrated success leading complex, cross-functional product development initiatives.
  • PMP certification strongly preferred.
  • Strong leadership and communication skills with the ability to influence without direct authority.
  • Experience managing multiple concurrent projects in a deadline-driven environment.
  • Familiarity with FDA regulatory pathways; experience with 510(k) submissions is a plus.
  • Analytical mindset with strong problem-solving and decision-making capabilities.

Compensation & Benefits

  • Competitive base salary ($130K–$160K, depending on experience)
  • Comprehensive health, dental, and vision coverage
  • Company 401(k) with match
  • Generous paid holidays (including your birthday!) and PTO
  • Wellness perks including gym membership subsidy
  • Employer-paid life, short-term, and long-term disability insurance
  • Health Savings Account (HSA) contributions

Why Join Us?

You’ll be part of a mission-driven organization focused on advancing healthcare through innovation and collaboration. This role offers both strategic influence and hands-on impact in shaping products that improve patient outcomes.

Job Tags

Temporary work,

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