Cell Therapy Quality Automation Director

Bristol Myers Squibb

Madison (NJ)

On-site

USD 188,250 - 228,114

Full time

14 days+
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Benefits offered by this job

Health Coverage
401(k) plan
Paid Time Off

Job summary

A leading biopharmaceutical company is seeking a Director of Cell Therapy Quality Automation in New Jersey. This global role involves leading quality initiatives to enhance manufacturing processes and ensure compliance with industry standards. The ideal candidate has 14+ years of experience in quality systems, strong leadership skills, and a proven track record in project management. This position offers competitive compensation and comprehensive benefits, promoting a balance between work and personal life.

Qualifications

  • Bachelor's degree in a relevant field (e.g., Engineering, Life Sciences); advanced degree preferred.
  • Extensive experience in quality systems and operations, typically achieved through 14+ years of experience.
  • Strong knowledge of industry standards and regulatory requirements related to quality systems.

Responsibilities

  • Lead the identification, execution, and implementation of quality solutions.
  • Collaborate with manufacturing, regulatory, and IT teams to ensure quality.
  • Drive compliance with industry best practices and regulatory requirements.

Skills

Leadership
Project management
Communication
Collaboration

Education

Bachelor's degree in relevant field
Advanced degree preferred

Tools

Quality systems knowledge

Job description

A leading biopharmaceutical company is seeking a Director of Cell Therapy Quality Automation in New Jersey. This global role involves leading quality initiatives to enhance manufacturing processes and ensure compliance with industry standards. The ideal candidate has 14+ years of experience in quality systems, strong leadership skills, and a proven track record in project management. This position offers competitive compensation and comprehensive benefits, promoting a balance between work and personal life.
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