Sr. Director, Sassenheim Quality Head & Global Lentivirus Operations

Johnson & Johnson MedTech

Sassenheim, Netherlands
Base: 127,900 eur to 221,145 eur annually includin...
Hybrid
Cgmp compliance and quality management
Quality assurance and quality control leadership
Global lentivirus supply chain management
Johnson & Johnson MedTech is seeking a Senior Director for Quality and Global Lentivirus Operations in Sassenheim, Netherlands. This strategic leadership role focuses on ensuring compliance with quality standards and cGMP regulations while managing quality assurance and control functions across multiple sites

Job Summary

  • The Senior Director leads all Quality functions at the Sassenheim site ensuring compliance with cGMP standards and Janssen’s quality requirements while managing a team of QA & QC professionals.
  • This role drives global consistency in Quality Operations across multiple sites and implements process changes to support scalable, compliant lentivirus production.
  • The position champions a culture of quality compliance, continuous improvement, and talent development while collaborating with cross-functional teams and external stakeholders.

Matching Summary

Match Score: 85

Johnson & Johnson MedTech is seeking a Senior Director for Quality and Global Lentivirus Operations in Sassenheim, Netherlands. This strategic leadership role focuses on ensuring compliance with quality standards and cGMP regulations while managing quality assurance and control functions across multiple sites.

Salary

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

Skills & Requirements

Must-have

  • cGMP compliance and quality management
  • Quality Assurance and Quality Control leadership
  • Global lentivirus supply chain management
  • Regulatory inspection readiness and audit leadership
  • Quality Management System (QMS) development
  • Team leadership and talent development
  • Cross-functional collaboration and stakeholder management

Nice-to-have

  • Strategic thinking and change sponsorship
  • Risk assessment and mitigation
  • Continuous improvement culture
  • Business acumen and budget management
  • Effective communication with health authorities
  • Inclusive leadership and diversity promotion

Key Requirements

  • University degree in pharmacy, engineering, chemistry, microbiology or related discipline
  • Minimum 12 years pharmaceutical industry experience
  • At least 12 years Quality Assurance and Quality Systems experience
  • Proven people management and quality leadership experience
  • Experience hosting global regulatory inspections
  • Fluent in English and Dutch (written and spoken)

Work Rights

Not specified

Tailored Resume

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