R&D Project Lead – Medical Devices (Catheters)

Midwest Interventional Systems Inc

Maple Grove (MN)

On-site

USD 75,000 - 100,000

Full time

14 days+

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Benefits offered by this job

Flexible PTO
Paid holidays
Health/Dental/Vision
Disability insurance
HSA with employer contrib
401(k) with employer contrib
Parental Leave

Job summary

Midwest Interventional Systems Inc. is seeking a Project Manager to guide R&D projects from concept to market on a contract basis, coordinating cross-functional teams and client relationships.

The role requires 1–3 years in project coordination or management, a degree in Business/Mechanical/Biomedical engineering, and familiarity with FDA QSR and ISO 13485. You will develop project plans, manage budgets, and serve as the primary client contact to drive on-time delivery and product success.

Qualifications

  • Bachelor's degree in Business, Mechanical, or Biomedical Engineering or equivalent experience.
  • 1-3 years of project coordination or management required.
  • Familiarity with FDA QSR and ISO 13485 regulations.
  • Strong client communication and ability to handle ambiguity.

Responsibilities

  • Directs product development from concept to market on contract basis.
  • Lead cross-functional teams and manage budgets and timelines.
  • Prepare project plans, risk analyses, and client proposals.
  • Serve as primary client contact and ensure delivery to customers.
  • Coordinate with suppliers and consultants as needed.

Skills

Project coordination
Client communication
Quality systems knowledge
FDA QSR knowledge
Statistics knowledge
Cross-functional teamwork

Education

Bachelor's degree in Business, Mechanical, or Biomedical Engineering

Job description

Midwest Interventional Systems Inc. is seeking a Project Manager to guide R&D projects from concept to market on a contract basis, coordinating cross-functional teams and client relationships.

The role requires 1–3 years in project coordination or management, a degree in Business/Mechanical/Biomedical engineering, and familiarity with FDA QSR and ISO 13485. You will develop project plans, manage budgets, and serve as the primary client contact to drive on-time delivery and product success.

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