Quality Strategy Lead – Global Compliance & Improvement

Johnson & Johnson Innovative Medicine

Raritan (NJ)

On-site

USD 122,000 - 213,000

Full time

10 days ago
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Job summary

Johnson & Johnson Innovative Medicine in Raritan, NJ is seeking a Senior Manager, Quality Strategy to shape and execute the integrated quality strategy across QA, QS, and QC. You will lead strategy and governance for quality initiatives at the site, partner with leadership, and drive regulatory readiness.

The role requires 8+ years in regulated QA/QC/Operations, strong leadership, and deep GMP knowledge. This position is based in Raritan, New Jersey with responsibility for Advanced Therapies

Qualifications

  • Bachelor’s degree in engineering, science, or related field.
  • 8+ years of experience in QA/QC/QS in a regulated environment.
  • Strong leadership and communication skills.
  • Proficiency with Microsoft Office and quality systems applications.

Responsibilities

  • Lead development and governance of the Raritan Quality portfolio across QA, QC, and QS.
  • Partner with local and cross-functional leaders to deploy quality improvement initiatives.
  • Drive continuous improvement across the Advanced Therapies Quality network.
  • Align quality strategy with site, platform, and enterprise goals.
  • Manage budgeting and resource planning for quality initiatives.
  • Ensure regulatory readiness and compliance across operations.

Skills

Quality Assurance
Quality Systems
Quality Control
Process Excellence
Lean Six Sigma
GMP Operations
Regulatory Knowledge
Leadership
Executive Communication

Education

Bachelor’s degree in engineering or science

Tools

Microsoft Word
Excel
PowerPoint
OneNote
TComet
truVault

Job description

Johnson & Johnson Innovative Medicine in Raritan, NJ is seeking a Senior Manager, Quality Strategy to shape and execute the integrated quality strategy across QA, QS, and QC. You will lead strategy and governance for quality initiatives at the site, partner with leadership, and drive regulatory readiness.

The role requires 8+ years in regulated QA/QC/Operations, strong leadership, and deep GMP knowledge. This position is based in Raritan, New Jersey with responsibility for Advanced Therapies

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