Sr. Director, Sassenheim Quality Head & Global Lentivirus Operations

J&J FAMILY OF COMPANIES

Sassenheim, Netherlands
Base: 127,900 eur to 221,145 eur; holiday allowanc...
Not specified (likely on-site due to leadership and compliance responsibilities)
Cgmp standards
Quality management system
Lentivirus operations
Johnson & Johnson is seeking a Senior Director for Quality and Global Lentivirus Operations at their Sassenheim facility in the Netherlands. This strategic leadership role involves overseeing quality management, ensuring compliance with cGMP standards, and fostering a culture of excellence within the organization

Job Summary

  • This role ensures strict compliance with cGMP standards and Janssen’s quality requirements, while establishing and maintaining robust Quality standards and systems across the site.
  • Beyond site-specific responsibilities, the role serves as the Quality partner to the Autologous Lentivirus Operations leader, focusing on compliantly expanding and scaling the global lentivirus supply chain across multiple locations.
  • Provides leadership to build a high-performing, collaborative team through hiring, mentoring, and talent development.

Matching Summary

Match Score: 85

Johnson & Johnson is seeking a Senior Director for Quality and Global Lentivirus Operations at their Sassenheim facility in the Netherlands. This strategic leadership role involves overseeing quality management, ensuring compliance with cGMP standards, and fostering a culture of excellence within the organization.

Salary

Base: 127,900 EUR to 221,145 EUR; Holiday Allowance: 8%; Benefits: Not specified

Skills & Requirements

Must-have

  • cGMP standards
  • Quality Management System
  • lentivirus operations
  • global regulatory agency inspections
  • Quality Assurance
  • Quality Control

Nice-to-have

  • inclusive work environment
  • culture of excellence
  • continuous improvement
  • strategic leadership role
  • risk assessment strategies

Key Requirements

  • University degree in pharmacy, engineering, chemistry, microbiology or related scientific / engineering discipline
  • At least 12 years’ working experience in the pharmaceutical industry
  • Minimum of 12 years of Quality Assurance / Quality Systems experience
  • Fluent in English and Dutch (written and spoken)

Work Rights

Not specified

Tailored Resume

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