Project Manager – Medical Devices (Operations / Manufacturing / Supply Chain)

Overview

On Site
Depends on Experience
Contract - Independent
Contract - W2
Contract - 12 Month(s)
No Travel Required
Unable to Provide Sponsorship

Skills

ISO 13485
Manufacturing
Medical Devices
Project Management
Regulatory Compliance
Supply Chain Management

Job Details

Project Manager – Medical Devices (Operations / Manufacturing / Supply Chain)

Location:
• Santa Rosa, CA – Onsite
• Minneapolis, MN – Onsite

Duration: Contract
Experience: 5+ Years (US Project Management experience required)

Job Description

We are seeking an experienced Project Manager with a strong background in the medical device industry to support cross-functional initiatives across Operations, Manufacturing, and Supply Chain. The ideal candidate will have hands-on experience working in FDA-regulated environments, managing complex projects, and driving data-backed insights to support operational excellence.

This is an onsite role requiring close collaboration with engineering, quality, operations, and supply chain teams.

Key Responsibilities

  • Lead end-to-end project management for medical device operations and manufacturing initiatives

  • Partner with Operations, Manufacturing, Supply Chain, Quality, and Engineering teams

  • Manage project scope, schedule, budget, risks, and dependencies

  • Drive process improvements across production, supply chain, and operational workflows

  • Ensure compliance with FDA regulations, GMP, and ISO 13485 standards

  • Track KPIs, analyze data, and present insights to stakeholders

  • Coordinate supplier-related and production planning activities

  • Deliver projects on time while maintaining quality and regulatory compliance

Required Skills & Qualifications

  • 5+ years of Project Management experience in the US

  • Experience within Medical Devices / Life Sciences / Regulated Manufacturing

  • Strong knowledge of:

    • Manufacturing Operations

    • Supply Chain & Vendor Management

    • Production Planning & Process Improvement

  • Familiarity with FDA, GMP, ISO 13485 environments

  • Strong analytical skills with ability to work with data and drive insights

  • Excellent communication and cross-functional collaboration skills

  • Ability to work 100% onsite at Santa Rosa, CA or Minneapolis, MN

Preferred Qualifications

  • PMP certification

  • Lean / Six Sigma experience

  • APICS / CPIM or supply-chain related certification

  • Experience with NPI (New Product Introduction) or Design Transfer projects

Work Authorization

  • Must be authorized to work in the US

Why This Role

  • High-impact projects in regulated medical device environments

  • Opportunity to work closely with manufacturing and operations leadership

  • Long-term contract potential

Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.

About Anagha Techno Soft