Associate Director, Quality Evaluations, Integrations, And External Services

Novartis UK

8 years pharmaceutical industry experience
R&d program knowledge preclinical clinical
Regulatory compliance fda glp gcp oecd
The role is primarily responsible for managing quality operational activities and leading due diligence in M&A and integration scenarios

Job Summary

  • The role is primarily responsible for managing quality operational activities and leading due diligence in M&A and integration scenarios.
  • Candidates must possess a deep understanding of international regulatory standards including FDA, GLP, and GCP to ensure compliance.
  • This position requires extensive experience in third-party vendor oversight, including CRO selection and performance monitoring.

Matching Summary

The role is primarily responsible for managing quality operational activities and leading due diligence in M&A and integration scenarios.

Skills & Requirements

Must-have

  • 8 years pharmaceutical industry experience
  • R&D program knowledge preclinical clinical
  • Regulatory compliance FDA GLP GCP OECD
  • Third-party vendor oversight and management
  • Quality due diligence execution and reporting

Nice-to-have

  • Familiarity with cell and gene platforms
  • Experience with chemical bioanalytical methods
  • Strong leadership and consensus building skills
  • Knowledge of animal welfare regulations
  • Ability to drive quality culture globally

Key Requirements

  • Ph.D. or Masters in Life Sciences
  • Minimum 8 years pharmaceutical industry experience
  • Expertise in R&D programs and quality assessments

Work Rights

Not specified

Tailored Resume

Cover Letter