Qa Manager-night Shift

Lilly

Concord, North Carolina, United States
Base: $94,500 - $138,600; bonus/equity: compyny bo...
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Bachelor's degree in science or engineering
5+ years pharmaceutical leadership experience
Gmp documentation review and approval
** Lilly is seeking a Night Shift Manager for Quality Assurance at its new Concord, North Carolina site, responsible for overseeing Device Assembly and Packaging operations. The ideal candidate will have extensive QA experience in the pharmaceutical industry, demonstrating leadership and technical expertise. **

Job Summary

  • The role involves providing technical oversight and leadership for the Device Assembly and Packaging workstream at Lilly's new Concord, North Carolina site.
  • Candidates will manage a team of up to 14 direct reports while ensuring compliance with cGMP regulations and supporting inspection readiness activities.
  • Lilly offers a comprehensive benefit program including medical, dental, vision, 401(k), pension, and a company bonus based on performance.

Matching Summary

Match Score: 75

** Lilly is seeking a Night Shift Manager for Quality Assurance at its new Concord, North Carolina site, responsible for overseeing Device Assembly and Packaging operations. The ideal candidate will have extensive QA experience in the pharmaceutical industry, demonstrating leadership and technical expertise. **

Salary

Base: $94,500 - $138,600; Bonus/Equity: Company bonus eligible; Benefits: Medical, dental, vision, 401(k), pension, vacation

Skills & Requirements

Must-have

  • Bachelor's degree in science or engineering
  • 5+ years pharmaceutical leadership experience
  • GMP documentation review and approval
  • Cross-functional technical project delivery
  • Night shift availability Monday through Friday

Nice-to-have

  • Strong interpersonal and communication skills
  • Ability to train and mentor others
  • Demonstrated problem-solving decision-making
  • Commitment to maintaining CSQA certification
  • Experience with highly automated combination products

Key Requirements

  • Bachelor's degree in science, engineering, or pharmaceutical field
  • 5+ years in pharmaceutical leadership with QA experience
  • Authorized to work in the United States full-time
  • ASQ CQM, CQE, or CQA certification preferred
  • Previous facility start-up and validation experience

Work Rights

Must be authorized to work in the US on a full-time basis

Tailored Resume

Cover Letter