Senior Director - Analytical Development And Quality Control

Eli Lilly UK

Base: $148,500 - $257,400; bonus/equity: eligible ...
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15 years industrial pharmaceutical experience
10 years qc management experience
Thorough knowledge of cgmps and ich guidance
** Eli Lilly UK is seeking a Senior Director of Analytical Development and Quality Control to oversee and enhance the analytical development functions for diagnostic radiopharmaceutical products. The ideal candidate will have extensive experience in pharmaceutical analytical development and quality control, with a strong focus on leadership and strategic innovation. **

Job Summary

  • The Senior Director will provide strategic technical leadership to drive analytical development and quality control strategies for diagnostic radiopharmaceutical products.
  • This role is accountable for building and developing a high-performing team through proactive coaching, structured mentoring, and workforce planning.
  • Eli Lilly offers a comprehensive benefit program including medical, dental, vision, 401(k), pension, and well-being benefits alongside a competitive salary range.

Matching Summary

Match Score: 75

** Eli Lilly UK is seeking a Senior Director of Analytical Development and Quality Control to oversee and enhance the analytical development functions for diagnostic radiopharmaceutical products. The ideal candidate will have extensive experience in pharmaceutical analytical development and quality control, with a strong focus on leadership and strategic innovation. **

Salary

Base: $148,500 - $257,400; Bonus/Equity: Eligible for company bonus based on performance; Benefits: Comprehensive program including 401(k), pension, medical, dental, vision, and wellness perks

Skills & Requirements

Must-have

  • 15 years industrial pharmaceutical experience
  • 10 years QC management experience
  • Thorough knowledge of cGMPs and ICH guidance
  • Experience with FDA CMC guidance
  • Leadership of scientific teams

Nice-to-have

  • Familiarity with radiochemistry
  • International travel capability
  • Strong project management skills
  • Cross-functional collaboration abilities
  • Strategic thinking capabilities

Key Requirements

  • PhD in chemistry or related field
  • Minimum 15 years in analytical development/QC
  • Minimum 10 years in QC management
  • Expertise in global cGMP regulations
  • Proven ability to manage competing priorities

Work Rights

Not specified

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