R&d Qa Manager - Gvp

Elvium

Cambridge, GB
Hybrid
Pharmacovigilance quality oversight
R&d audit planning and execution
Vendor quality management
The R&D QA Manager will act as a guardian of patient safety and regulatory compliance within the Pharmacovigilance quality assurance team

Job Summary

  • The R&D QA Manager will act as a guardian of patient safety and regulatory compliance within the Pharmacovigilance quality assurance team.
  • This role offers opportunities for learning and development within a collaborative and inclusive work environment that values diversity and authenticity.
  • Mundipharma is a global healthcare company dedicated to innovative treatments, guided by principles of integrity and patient-centricity.

Matching Summary

The R&D QA Manager will act as a guardian of patient safety and regulatory compliance within the Pharmacovigilance quality assurance team.

Skills & Requirements

Must-have

  • Pharmacovigilance quality oversight
  • R&D audit planning and execution
  • Vendor quality management
  • GVP compliance expertise
  • Regulatory inspection support
  • CAPA and deviation management

Nice-to-have

  • Flexible hybrid working
  • Collaborative inclusive environment
  • Diversity and inclusion focus
  • Strong reporting and analysis skills
  • Autonomous risk-based decision making

Key Requirements

  • Scientific degree in Pharmacy, Chemistry, Biology, Engineering or similar
  • Certification in Quality Systems Management or auditing
  • Extensive QA experience in Pharmaceutical or Medical Devices industry
  • Proven GVP knowledge and regulatory interaction experience
  • Working knowledge of GCP preferred

Work Rights

Not specified

Tailored Resume

Cover Letter