Associate Director - Qms Lifecycle Management (r&d)

Eli Lilly UK

Us, India
$115,500 - $169,400; not specified; comprehensive ...
On-site
R&d business partner for qms
Support qms process framework
Implement standards, governance, and metrics
Eli Lilly UK is seeking an Associate Director for QMS Lifecycle Management focused on R&D processes, responsible for ensuring the integrity and implementation of the Quality Management System. The ideal candidate will have over seven years of experience in the pharmaceutical industry with a strong background in R&D, quality assurance, and operational roles

Job Summary

  • The Associate Director, QMS Lifecycle Management (R&D Focus) serves as the R&D business partner within the Lifecycle Management pillar of the Quality Management System (QMS).
  • This role supports the integrity and evolution of the QMS process framework for R&D-relevant processes by partnering with Global Process Owners (GPOs) and key stakeholders to implement standards, governance, and metrics.
  • The incumbent is accountable for day-to-day coordination, health monitoring, and reporting for the R&D-relevant portion of the Lifecycle Management pillar, escalating risks, trends, and improvement opportunities to the Operational Controls Lead.

Matching Summary

Match Score: 85

Eli Lilly UK is seeking an Associate Director for QMS Lifecycle Management focused on R&D processes, responsible for ensuring the integrity and implementation of the Quality Management System. The ideal candidate will have over seven years of experience in the pharmaceutical industry with a strong background in R&D, quality assurance, and operational roles.

Salary

$115,500 - $169,400; Not specified; Comprehensive benefit program

Skills & Requirements

Must-have

  • R&D business partner for QMS
  • support QMS process framework
  • implement standards, governance, and metrics
  • monitor and report QMS health
  • identify process improvement opportunities

Nice-to-have

  • strong strategic thinking capability
  • demonstrated change agility
  • balance speed, quality, and risk
  • lead through influence in a matrixed environment

Key Requirements

  • 7+ years experience in pharmaceutical industry
  • Bachelor's degree in Life Science
  • Experience supporting cross-functional initiatives
  • Ability to drive process improvements through data analysis
  • Expertise in global regulatory standards for R&D

Work Rights

Not specified

Tailored Resume

Cover Letter