Sr. Scientist Biologics Ad

Johnson & Johnson

Schaffhausen, Switzerland
**
Container closure integrity testing (ccit)
Cell and gene therapy analytics
Antibody drug conjugate analytics
** Johnson & Johnson is seeking a Senior Scientist for their Particulates and Container Closure Integrity (PCCI) team in Schaffhausen, Switzerland. The role involves project coordination, method validation, and supporting biotherapeutic products in a GMP-regulated environment. **

Job Summary

  • The Particulates and Container Closure Integrity (PCCI) team is a development lab within the global Janssen Research & Development organization embedded in the GMP environment of the Johnson&Johnson Innovative Medicine Supply Chain (IMSC).
  • In this position, you are responsible for further developing the center of excellence (CoE) for container closure integrity testing (CCIT) for products in the cell and gene therapy, antibody and antibody drug conjugate space, building up, growing, and coordinating laboratory analytics for CCI testing.
  • After a thorough on-the-job training, you will have responsibility for project coordination, method validations and transfers to manufacturing sites and commercial quality control laboratories, drafting regulatory submissions and supporting marketed products.

Matching Summary

Match Score: 75

** Johnson & Johnson is seeking a Senior Scientist for their Particulates and Container Closure Integrity (PCCI) team in Schaffhausen, Switzerland. The role involves project coordination, method validation, and supporting biotherapeutic products in a GMP-regulated environment. **

Skills & Requirements

Must-have

  • Container Closure Integrity Testing (CCIT)
  • cell and gene therapy analytics
  • antibody drug conjugate analytics
  • GMP-regulated development environment
  • method validations and transfers

Nice-to-have

  • self-employed and entrepreneurial style
  • curiosity and drive
  • team-oriented environment
  • respect diversity and inclusion

Key Requirements

  • M.S. with at least 5 years’ experience or PhD with at least 2 years’ experience
  • Experience within the pharmaceutical or GMP-regulated industry preferred
  • Excellent communication skills in English (written and spoken)

Work Rights

Not specified

Tailored Resume

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