Sr. Director, Sassenheim Quality Head & Global Lentivirus Operations
Johnson & Johnson
Sassenheim, Netherlands
Base: 127,900 eur to 221,145 eur annually; bonus/e...
12 years pharmaceutical quality experience
Cgmp compliance for lentivirus manufacturing
Qualified person deputy authority
This strategic leadership role oversees all Quality functions at the Johnson & Johnson Sassenheim site while driving global consistency across multiple international locations
Job Summary
This strategic leadership role oversees all Quality functions at the Johnson & Johnson Sassenheim site while driving global consistency across multiple international locations.
The incumbent acts as a Deputy Qualified Person with independent decision-making authority on product release and rejection of non-conforming products.
The position requires extensive experience hosting global regulatory agency inspections and fostering a culture of continuous improvement within a diverse, inclusive environment.
Matching Summary
This strategic leadership role oversees all Quality functions at the Johnson & Johnson Sassenheim site while driving global consistency across multiple international locations.
Salary
Base: 127,900 EUR to 221,145 EUR annually; Bonus/Equity: Not specified; Benefits: 8% holiday allowance included
Skills & Requirements
Must-have
12 years pharmaceutical quality experience
cGMP compliance for lentivirus manufacturing
Qualified Person deputy authority
Global regulatory inspection leadership
QA/QC team management and development
Nice-to-have
Aseptic processing in ISO 5 clean rooms
Biosafety cabinet operation experience
Fluent Dutch language skills
CAR-T cell therapy background
Strategic change sponsorship mindset
Key Requirements
University degree in pharmacy, engineering, chemistry, or microbiology
Minimum 12 years in pharmaceutical quality leadership
Comprehensive knowledge of vaccines and biological manufacturing
Proven track record in building QA/QC teams
Experience with commercial cGMP manufacturing operations