Analytical Qc & As&t Expert

Novartis UK

Analytical method validation and transfer
Gmp glp qms compliance expertise
Oos investigation and capa implementation
The role involves leading analytical release testing, investigational support, and stability testing within a highly skilled laboratory environment

Job Summary

  • The role involves leading analytical release testing, investigational support, and stability testing within a highly skilled laboratory environment.
  • Candidates must ensure strict compliance with GMP, GLP, QMS, and pharmacopoeia standards while managing method lifecycles.
  • Novartis seeks to reimagine medicine by leveraging experienced associates who drive quality, safety, and efficiency in their operations.

Matching Summary

The role involves leading analytical release testing, investigational support, and stability testing within a highly skilled laboratory environment.

Skills & Requirements

Must-have

  • Analytical method validation and transfer
  • GMP GLP QMS compliance expertise
  • OOS investigation and CAPA implementation
  • Stability study coordination
  • Laboratory equipment qualification

Nice-to-have

  • Continuous improvement project experience
  • Risk management initiatives
  • Cross-functional stakeholder collaboration
  • New technology evaluation skills

Key Requirements

  • Master degree in pharmacy or chemistry
  • At least 5 years in QC department
  • Fluent in Italian language
  • Good knowledge of English

Work Rights

Not specified

Tailored Resume

Cover Letter