Cross-Functional Medical Device R&D Project Manager

Medline Industries, Inc.

Northfield (MN)

On-site

USD 92,000 - 138,000

Full time

5 days ago
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Job summary

Medline Industries, LP in Minnesota seeks a Product Development Project Manager to guide development of medical devices, dietary supplements, cosmetics, and OTC/ANDA/NDA drugs. You will manage all aspects of projects and lead cross-functional teams across R&D, quality, regulatory, manufacturing, and product divisions.

The role requires a Bachelor's in engineering or science and at least 2 years in medical device or pharma. PMP is preferred. Domestic/international travel up to 10% may be required.

Qualifications

  • Bachelor's degree in engineering or science field (required).
  • Minimum 2 years of experience in medical device or pharmaceutical field.
  • Knowledge of design controls, risk assessments, and 510(k) process.
  • Willingness to travel up to 10% (domestic and international).

Responsibilities

  • Guide and manage a portfolio of product development projects across medical devices, supplements, cosmetics, and OTC drugs.
  • Lead cross-functional teams including R&D, quality, regulatory, manufacturing, and product divisions.
  • Develop, communicate, and track project plans, objectives, budgets, scope, and timelines.
  • Conduct risk assessments and develop contingency plans to mitigate delays or cost overruns.
  • Represent Medline on ASTM/AAM/ISO committees and contribute to new test standards.
  • Maintain team morale and ensure transparent, ongoing communication.

Skills

Project management
Medical device knowledge
Risk assessments
Design controls
510(k) process
Travel up to 10%

Education

Bachelor's degree in Engineering or Science related field

Tools

Microsoft Project

Job description

Medline Industries, LP in Minnesota seeks a Product Development Project Manager to guide development of medical devices, dietary supplements, cosmetics, and OTC/ANDA/NDA drugs. You will manage all aspects of projects and lead cross-functional teams across R&D, quality, regulatory, manufacturing, and product divisions.

The role requires a Bachelor's in engineering or science and at least 2 years in medical device or pharma. PMP is preferred. Domestic/international travel up to 10% may be required.

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