Quality Director

J&J FAMILY OF COMPANIES

Wilson, North Carolina, United States
Hybrid (onsite in wilson, nc, with some travel to greater philadelphia during the project design phase)
Quality control testing management
Quality assurance review and approval
Compliance and regulatory activities
Johnson & Johnson is seeking a Quality Director for their new biologics manufacturing facility in Wilson, North Carolina. This leadership role will oversee all quality-related programs and activities, ensuring compliance and operational excellence within the organization's standards

Job Summary

  • J&J is expanding manufacturing capacity with a $2 billion investment to support portfolio growth and deliver breakthrough biologic medicines.
  • The Quality Director will lead all quality aspects from design through construction, commissioning, and regulatory approval of a new biotherapeutic manufacturing facility.
  • Johnson & Johnson provides an inclusive work environment that respects diversity and promotes organizational excellence.

Matching Summary

Match Score: 85

Johnson & Johnson is seeking a Quality Director for their new biologics manufacturing facility in Wilson, North Carolina. This leadership role will oversee all quality-related programs and activities, ensuring compliance and operational excellence within the organization's standards.

Skills & Requirements

Must-have

  • Quality Control testing management
  • Quality Assurance review and approval
  • Compliance and regulatory activities
  • Product Release decision authority
  • GMP regulations application
  • Cross-functional team collaboration
  • Quality culture development

Nice-to-have

  • Mentoring and coaching staff
  • Financial leadership and budgeting
  • Innovative and tenacious mindset
  • Strong interpersonal skills
  • Change management leadership
  • Detail-oriented with big picture focus
  • Ethical and Credo-based decision making

Key Requirements

  • Bachelor’s degree in science or engineering
  • 10-15 years leadership in biological/pharmaceutical industry
  • 5 years Quality leadership experience
  • Experience with FDA/EMEA biologics regulations
  • Proven global organization management
  • Strong knowledge of regulatory compliance
  • Ability to apply GMP and international guidelines

Work Rights

Not specified

Tailored Resume

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