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Regulatory Project Manager IV

Permanente, CA 95014

Posted: 06/13/2024 Employment Type: Contract Job Category: Project Management Job Number: 605375 Is job remote?: Yes Country: United States

Job Description

Target Pay Rate: 70-100/hr **salary will be commensurate with experience 

Job Description: 

The Program Manager will provide regulatory and quality support for product submissions, approvals, and launch readiness. You will work hand in hand with cross- functional teams and may provide hands-on individual contribution to meet the team’s objectives. You will be responsible for developing program timelines, tracking submission deliverables, and providing support for regulatory submissions by coordinating with various team members. You will collaborate closely with multiple cross-functional teams to drive global product launch readiness. In addition, you will drive day-to day program activities, generate and own reports and score cards, and conduct risk assessments to meet overall program objectives.

Responsibilities include:
  • Oversee regulatory submissions and approvals for portfolios of work
  • Establish a robust understanding of the overall critical path to coordinate activities and resolve problems alongside cross-functional partners
  • Communicate program status and escalate risks to a variety of stakeholders
  • Establish and manage Quality Design History File documentation timelines and successful execution across multiple cross-functional stakeholders
Key Qualifications:
  • 8+ years of program/project management experience in a regulated industry, preferably in medical products and/or digital health
  • Proven track record of driving regulatory submissions, approvals, and launches with multi-disciplinary teams
  • Outstanding communication and organizational skills. Ability to optimally manage multiple projects simultaneously
  • Excellent analytical and problem-solving capabilities, with a keen eye to detect and mitigate risks
  • Independent self-starter who thrives in ambiguous environments
  • Hands-on experience in the use of project management and reporting software
Additional Requirements:
  • Experience with Design Controls and Quality Systems
  • Solid understanding of regulatory process for different classes of medical devices in both the US and internationally
  • May require occasional travel
Education & Experience:
  • BS/MS in Engineering, Biomedical Science or equivalent science degree.

**CO/NY candidates may not be considered 

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About Permanente, CA

Ready to embark on a thrilling career journey in vibrant Permanente, California? Nestled in the heart of Silicon Valley, this region boasts an exceptional blend of innovation and natural beauty, with job opportunities as enticing as the view from the top of nearby Mount Hamilton. From tech startups to renowned companies like Google and Apple, Permanente is a hotbed for professional growth in diverse industries. With the verdant trails of Rancho San Antonio County Park, the striking artworks at the Cantor Arts Center, and performances at the Mountain View Center for the Performing Arts, Permanente offers a rich tapestry of cultural experiences. Don't miss out on the chance to write the next chapter of your career story in this dynamic and enchanting location - explore our job listings today!

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