Sr. Manager, Product Quality Integrator

Johnson & Johnson

Beerse, Antwerp, Belgium
Quality strategy and compliance management
Global quality liaison and communication
Health authority submission review and approval
The Senior Manager, Product Quality Integrator has end-to-end accountability for the quality strategy and quality aspects from Early Development through commercialization in Launch and Grow for an assigned group of large molecules (biological) products

Job Summary

  • The Senior Manager, Product Quality Integrator has end-to-end accountability for the quality strategy and quality aspects from Early Development through commercialization in Launch and Grow for an assigned group of large molecules (biological) products.
  • Johnson & Johnson provides an inclusive work environment where each person is considered as an individual and respects the diversity and dignity of employees.
  • This position supports global quality processes, drives decision making and problem solving, and collaborates with cross-functional teams to ensure patients receive the right quality products.

Matching Summary

The Senior Manager, Product Quality Integrator has end-to-end accountability for the quality strategy and quality aspects from Early Development through commercialization in Launch and Grow for an assigned group of large molecules (biological) products.

Skills & Requirements

Must-have

  • Quality strategy and compliance management
  • Global Quality liaison and communication
  • Health authority submission review and approval
  • Quality assurance in biotherapeutics manufacturing
  • Cross-functional team leadership
  • Risk assessment and problem solving
  • cGMP standards knowledge

Nice-to-have

  • Mentorship and team development
  • Flexible work hours across global regions
  • Experience with technology transfer and process validation
  • Quality content development for regulatory filings
  • Collaboration with external manufacturers
  • Business continuity process support
  • Quality complaint trend analysis

Key Requirements

  • Bachelor’s degree in Pharmacy, Biology, Biochemistry, Biotechnology, Engineering or similar
  • Minimum 8 years pharmaceutical or biotechnology industry experience
  • Knowledge of cGMP standards and policies
  • Ability to work across organizational boundaries
  • Flexible hours for US, EMEA, and ASPAC schedules
  • Up to 10% domestic and international travel
  • Preferred Master’s or advanced degree

Work Rights

Not specified

Tailored Resume

Cover Letter