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R&D Project Manager; Medical Devices

Job in Santa Clara, Santa Clara County, California, 95053, USA
Listing for: ManpowerGroup Global, Inc.
Full Time position
Listed on 2026-02-01
Job specializations:
  • Healthcare
    Healthcare Management
  • Management
    Healthcare Management
Salary/Wage Range or Industry Benchmark: 50 - 53 USD Hourly USD 50.00 53.00 HOUR
Job Description & How to Apply Below
Position: R&D Project Manager (Medical Devices)

Job Title: R&D Project Manager (Medical Devices)
Location: 3200 Lakeside Dr, Santa Clara, CA 95054
Duration: 12 Months
Work Arrangement: 100% Onsite
Pay Range: $50–$53 per hour (W2)

Role Overview

The R&D Project Manager will be responsible for planning, executing, and delivering cross‑functional projects within scope, schedule, and budget. This role requires strong project management skills, experience working in regulated environments, and the ability to communicate effectively with senior leadership, suppliers, and internal teams.

Key Responsibilities
  • Define and manage overall project scope, including development of project charters and detailed project plans
  • Identify key milestones and provide regular project status updates to stakeholders
  • Manage project schedules, resources, budgets, risk assessments, and documentation
  • Lead cross‑functional teams to execute project tasks, resolve issues, and achieve agreed‑upon deliverables
  • Drive teams to meet milestones and commitments aligned with senior leadership expectations
  • Prepare and present data‑driven reports and presentations using advanced Excel and Power BI for senior leadership
  • Track budget performance, report variances, and recommend contingency plans as needed
  • Lead meetings with internal cross‑functional teams and external suppliers
  • Document and distribute meeting minutes, including decisions and action items
  • Foster a collaborative work environment that supports team effectiveness
  • Ensure compliance with FDA regulations and quality standards, including ISO 9001 and ISO 13485
  • Support and collaborate on supplier process validation activities
Required Experience
  • 3–6 years of experience in an FDA‑regulated industry

We are looking for a candidate who is eligible to work with any employer without sponsorship. If you’re interested, please click “Apply” button.

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