Associate - Qa Representative - Floor Support

Lilly

Concord, North Carolina, United States
Base: $65,250 - $169,400; bonus/equity: compyny bo...
Onsite (8-12 hour shifts required, not eligible for remote work)
3+ years pharmaceutical quality experience
5+ years regulated manufacturing industry
Cgmp compliance and documentation knowledge
Lilly is seeking a Quality Assurance Representative for their new manufacturing facility in Concord, North Carolina. The role involves ensuring GMP compliance and providing quality oversight during the design and startup of the facility, requiring a strong background in pharmaceutical manufacturing

Job Summary

  • Lilly is investing over $1 billion to build a new state-of-the-art manufacturing site in Concord, North Carolina.
  • The Quality Assurance Representative will provide guidance on GMP compliance during the design, verification, and startup of manufacturing areas.
  • Employees are eligible for a company bonus, comprehensive benefits including medical and dental, and participation in a 401(k) plan.

Matching Summary

Match Score: 85

Lilly is seeking a Quality Assurance Representative for their new manufacturing facility in Concord, North Carolina. The role involves ensuring GMP compliance and providing quality oversight during the design and startup of the facility, requiring a strong background in pharmaceutical manufacturing.

Salary

Base: $65,250 - $169,400; Bonus/Equity: Company bonus depending on performance; Benefits: Medical, dental, vision, 401(k), vacation

Skills & Requirements

Must-have

  • 3+ years pharmaceutical quality experience
  • 5+ years regulated manufacturing industry
  • cGMP compliance and documentation knowledge
  • Bachelor's degree in scientific field
  • Onsite work availability required

Nice-to-have

  • Cross-functional team communication skills
  • Mentoring and training capabilities
  • Strong technical writing experience
  • Ability to work independently as SME
  • Fostering a strong quality culture

Key Requirements

  • 3+ years Quality pharmaceutical manufacturing experience
  • 5+ years pharmaceutical or regulated manufacturing experience
  • Bachelor's degree in scientific field
  • Ability to work onsite 8-12 hour shifts
  • ASQ Certified CSQA preferred

Work Rights

Not specified

Tailored Resume

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