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Sr. Project Manager, RAQA

Role overview

Qualifications

  • Bachelor’s degree (BA/BS) or equivalent
  • PMP certification or equivalent preferred
  • Minimum of 7 years of project management experience, preferably within medical device, life sciences, pharmaceutical, or other regulated industry
  • Strong knowledge of project management methodologies and tools

Responsibilities

  • Lead medium to high complexity cross-functional RAQA projects from initiation through completion
  • Develop and maintain project plans, schedules, and related documentation
  • Coordinate activities across multiple functional teams and partners
  • Monitor project progress and communicate status, risks, issues, and mitigation plans to stakeholders

Key facts

Other skills

  • Planning
  • Prioritization
  • Social Skills
  • Communication
  • Presentations
  • Problem Solving
  • Critical Thinking
  • Decision Making

About the company

VB Spine logo

VB Spine

Unknown

Company details

Company size1001 - 5000

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Job description

Sr. Project Manager, RAQA
Location: Leesburg, VA, Allendale, NJ or Remote

Company: VB Spine

Looking for a career where your work truly matters? At VB Spine, you’ll be part of a mission-focused team that supports surgeons during life-changing spinal procedures. We’re the largest privately held spine company and among the largest family-owned medical technology companies in the world, dedicated to innovation, surgeon partnerships, and improving patient outcomes in spine care. As a Sr. Project Manager, RAQA in our Regulatory Affairs & Quality Assurance function within the Spine division, you’ll lead large, complex, cross-functional projects that support regulatory compliance, quality systems, product lifecycle management, and critical business objectives.


What You’ll Do:

  • Lead medium to high complexity cross-functional RAQA projects from initiation through completion
  • Develop and maintain project plans, schedules, budgets, resource plans, communication plans, and related documentation
  • Partner with functional leaders to define project scope, objectives, deliverables, milestones, and success criteria
  • Coordinate activities across Regulatory Affairs, Quality Assurance, R&D, Operations, Supply Chain, Manufacturing, Clinical, Marketing, Finance, and external partners
  • Facilitate cross-functional meetings and ensure decisions, action items, risks, and dependencies are documented and managed
  • Monitor project progress and communicate status, risks, issues, and mitigation plans to stakeholders and leadership
  • Identify project risks and develop mitigation and contingency plans
  • Manage project scope, schedule, cost, and quality while balancing competing priorities
  • Drive resolution of project issues through collaboration across functional teams
  • Support implementation of new regulatory requirements, quality initiatives, remediation activities, product changes, and compliance projects
  • Ensure projects comply with internal quality system requirements and applicable global regulatory standards
  • Track project financials, including budget forecasts and actual expenditures
  • Support continuous improvement of project management processes, tools, and best practices
  • Provide coaching and mentoring to less experienced project managers and team members
  • Present project updates and recommendations to senior management and project sponsors

What You Bring:

  • Bachelor’s degree (BA/BS) or equivalent (emphasis in management or related discipline preferred)
  • PMP certification or equivalent (e.g., PRINCE2) preferred
  • Minimum of 7 years of project management experience, preferably within medical device, life sciences, pharmaceutical, or other regulated industry
  • Experience with quality systems, regulatory compliance, product development, or manufacturing projects preferred
  • Strong knowledge of project management methodologies and tools (Microsoft Project, SharePoint, Visio, etc.)
  • Working knowledge of Quality Management Systems (QMS) and global regulatory requirements (FDA, ISO 13485, MDR, etc.)
  • Understanding of design controls, change management, CAPA, complaint handling, risk management, and product lifecycle processes
  • Excellent planning, organization, prioritization, interpersonal, facilitation, communication, and presentation skills
  • Demonstrated ability to influence without direct authority and drive consensus
  • Strong problem-solving, critical thinking, and decision-making skills
  • Ability to manage multiple priorities in a fast-paced, changing environment

Why VB Spine?
We believe in growing talent from within. At VB Spine, join a high-performing team where you’ll lead critical RAQA projects that strengthen compliance, quality, and product lifecycle excellence — supporting the delivery of innovative spinal solutions that improve patient lives.

Compensation:
Pay for this role is competitive and based on experience, qualifications, and performance. The typical pay range for this position is $125,000.00 - $145,000.00 annually, with potential for bonuses and incentives plus benefits. Final compensation is determined on a case-by-case basis and considers a variety of factors including experience level, skillset, and market conditions.

Benefits include:

  • Comprehensive health, dental, and vision insurance
  • 401(k) with company match
  • Paid time off (PTO) and holidays
  • Ongoing training and professional development opportunities
  • Opportunity to grow within a fast-paced, dynamic company

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MR

Marcus Rivera

Chief Revenue Officer

m.rivera@company.com
linkedin.com/in/marcusrivera
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