Sr. Director, Sassenheim Quality Head & Global Lentivirus Operations

Johnson & Johnson Innovative Medicine

Sassenheim, Netherlands
Base: 127,900 eur to 221,145 eur annually; bonus/e...
Not specified (potentially hybrid based on industry standards)
Cgmp compliance and quality management
Quality assurance and quality control leadership
Global lentivirus supply chain management
Johnson & Johnson is seeking a Senior Director for Quality and Global Lentivirus Operations in Sassenheim, Netherlands. This leadership role focuses on ensuring compliance with quality standards and managing a team to drive high-quality product supply in the pharmaceutical sector

Job Summary

  • The Senior Director leads all Quality functions at the Sassenheim site, ensuring compliance with cGMP standards and driving long-term quality strategies for clinical and commercial manufacturing.
  • This role also partners globally to harmonize quality operations across multiple sites, promoting scalable and compliant lentivirus production.
  • The position emphasizes building a high-performing quality team, fostering a culture of excellence, and maintaining strong relationships with regulatory authorities and internal stakeholders.

Matching Summary

Match Score: 85

Johnson & Johnson is seeking a Senior Director for Quality and Global Lentivirus Operations in Sassenheim, Netherlands. This leadership role focuses on ensuring compliance with quality standards and managing a team to drive high-quality product supply in the pharmaceutical sector.

Salary

Base: 127,900 EUR to 221,145 EUR annually; Bonus/Equity: Not specified; Benefits: 8% holiday allowance

Skills & Requirements

Must-have

  • cGMP compliance and quality management
  • Quality Assurance and Quality Control leadership
  • Global lentivirus supply chain management
  • Regulatory inspection readiness
  • Quality Management System (QMS) expertise
  • Team leadership and talent development

Nice-to-have

  • Strategic thinking and change sponsorship
  • Risk assessment and mitigation skills
  • Effective negotiation and influencing
  • Business acumen and budget management
  • Fluent English and Dutch communication
  • Culture of continuous improvement

Key Requirements

  • University degree in pharmacy, engineering, chemistry, microbiology or related field
  • At least 12 years pharmaceutical industry experience
  • Minimum 12 years Quality Assurance/Quality Systems experience
  • Experience with vaccines and biological manufacturing quality management
  • Proven people management and leadership experience
  • Experience hosting global regulatory inspections
  • Fluent in English and Dutch

Work Rights

Not specified

Tailored Resume

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