Project Manager

  • $58–$60 Per Hour

Highlights

Collaborate with top-tier teams in Regulatory Affairs, Quality, R&D, Supply Chain, and Commercial Operations, contributing to impactful projects that shape the future of clinical diagnostics. Join a pioneering leader in the diagnostics industry as a Project Manager driving critical IVDR Technical File assembly and Label Cutover initiatives.

Numbers & Facts

LocationFremont, CA
Salary$58–$60 Per Hour

Description

  • Current Openings
  • Veterans Program
  • Working With Indotronix
  • Referral Program

All current openings

Project Manager

  • Location: Fremont, California 94538
  • Work model: On-site
  • Posted July 8, 2026
  • Job ID: JPC - 206069

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Job Description

Project Manager - IVDR Technical Files & Label Cutover

Location: Fremont, CA (Contract)

Division: Clinical Diagnostics - Niche Diagnostics

About the Role

Join a pioneering leader in the diagnostics industry as a Project Manager driving critical IVDR Technical File assembly and Label Cutover initiatives. You will play a central role in ensuring regulatory compliance and the successful transition of product labeling across a diverse diagnostics portfolio. Collaborate with top-tier teams in Regulatory Affairs, Quality, R&D, Supply Chain, and Commercial Operations, contributing to impactful projects that shape the future of clinical diagnostics.

Responsibilities

  • Lead end-to-end management of IVDR Technical File and labeling projects, from initiation through implementation
  • Develop, track, and update comprehensive project plans, timelines, risk registers, and status reports
  • Coordinate cross-functional teams to achieve deliverables on schedule and escalate issues as needed
  • Facilitate project meetings and ensure timely execution of action items
  • Support change management for product labeling and regulatory submissions
  • Collaborate across Regulatory, Quality, Operations, Supply Chain, Manufacturing, and Marketing to align project goals
  • Maintain accurate project documentation in accordance with quality and regulatory standards
  • Track readiness, inventory, and cutover milestones for successful product transition
  • Identify and mitigate risks impacting regulatory timelines or market continuity

Required Skills and Experience

  • Bachelor's degree in Life Sciences, Engineering, Business, Regulatory Affairs, or related field
  • 3-5 years' experience in project management, coordination, regulatory, quality, or operations within a regulated industry (medical device, diagnostics, healthcare)
  • Proven track record managing cross-functional projects with multiple stakeholders
  • Strong organizational and communication skills with attention to detail
  • Proficiency in Smartsheet, Excel, PowerPoint, and collaboration tools
  • Ability to manage multiple priorities in a dynamic environment
  • Effective facilitator with a proactive, collaborative mindset

Preferred Skills

  • Exposure to IVDR or regulated product environments
  • Experience with regulatory compliance, labeling changes, or technical documentation projects
  • Knowledge of medical device or diagnostic regulatory requirements

Benefits

  • Opportunity to make a significant impact in a globally recognized diagnostics division
  • Professional growth through collaboration with industry leaders and exposure to cutting-edge regulatory projects
  • Supportive, innovative, and cross-functional team environment
  • Flexible contract role with potential for extension

How to Apply

Ready to advance your career in diagnostics project management? Submit your application and join a team dedicated to excellence, innovation, and compliance.

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Interested in this role?

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Job details

Job ID JPC - 206069

Location Fremont, California, United States

Work Model On-site

Job Type Contract

Experience 2-5 years

Industry Healthcare - Health Services

Pay Rate $58 - $60 (Hourly)

Posted July 8, 2026

Skills Project Management Project Coordination regulatory quality operations

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