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Project Engineer – Medical Device Development

8 Oct 2025
Verified by Turrior

Content + Source + Freshness • 13 Dec 2025 • 95% confidence

78 / 100

Offer value

Moderate value influenced by the technical nature of the role and its reliance on regulatory compliance in medical device development.

  • Significant involvement in innovative medical device projects.
  • Collaborative cross-functionality enhances skill diversity.
  • Requires dedicated work within strict regulatory boundaries.
Pros
  • Involvement in significant medical device projects promoting innovation.
  • Collaboration with multidisciplinary teams enhances exposure and learning.
  • Strong industry relevance leading to robust future opportunities.
Cons
  • High stakes as role directly impacts product safety and regulatory compliance.
  • Potential for long hours and intense project timelines.
  • Onsite requirement may limit flexibility for some candidates.

Who it's for

Mid-Level • Onsite

Good fit
  • Engineers experienced in the medical devices sector.
  • Mid-level professionals seeking to grow their project management expertise.
  • Individuals passionate about healthcare technology.
Not recommended for
  • Recent graduates or those lacking relevant experience.
  • Candidates desiring fully remote roles.
  • Individuals who prefer low-pressure environments.

Motivation fit

Desire to innovate within the medical device category.Interest in enhancing project management and collaboration skills.Commitment to ensuring product safety and compliance.

Key skills

Project management expertise in engineering contexts.Cross-functional team collaboration.Knowledge of regulatory requirements and documentation.Technical documentation proficiency.
Score: 78/100 AI verified analysis

About the job

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Project Engineer – Medical Device Development

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Location: Minnetonka, Minnesota, USA (100% Onsite)
Locals Preferred
Experience: 3-5 years

Key Responsibilities
-Develop and manage project plans, budgets, schedules, and risk registers.
-Drive design and development of medical devices in compliance with regulatory standards.
-Collaborate with cross-functional teams (engineering, quality, regulatory) to ensure alignment and compliance.
-Oversee product testing, validation, and verification activities.
-Maintain accurate documentation to support regulatory submissions and product lifecycle management.
-Primary Focus: Advance alternate source projects to completion (currently 4 active projects).
-Collaboration: Work with internal teams and external suppliers to meet project goals.
Nature of Role:
-Approximately 70% project management
-Approximately 30% task coordination (tasks largely handled by other team members)
-Tools: Uses Microsoft Project for project management (familiarity preferred, not required).
-Background: Engineering background preferred; experience in any technical field will also be considered.
Work Style: Highly deadline-driven, capable of managing multiple ongoing initiatives.

Core Skills
-Project management
-Cross-functional collaboration
-Regulatory compliance
-Technical documentation
-Strong communication skills

Education & Experience
-Bachelor’s degree (other degrees acceptable with relevant experience).
-3-5 years of work experience.

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