Scientist - Qa Parenteral

Eli Lilly

Research Triangle Park, North Carolina, USA
$65,250 - $169,400; bonus/equity: compyny bonus; b...
Onsite
Cgmp expert
Parenteral manufacturing quality
Verification and validation oversight
Eli Lilly is seeking a Scientist for their Quality Assurance team in the new Parenteral, Device, and Packaging Assembly Facility in Research Triangle Park, North Carolina. The ideal candidate will have extensive experience in parenteral manufacturing quality assurance, particularly in cGMP compliance, and will play a crucial role in the design and startup phases of the facility

Job Summary

  • The Quality Assurance Representative is responsible for demonstrating leadership, teamwork, and quality and regulatory knowledge and oversight to provide guidance, consultation and influence in the design, verification, and startup of the parenteral areas.
  • Act as a cGMP expert, working with Global Facility Delivery, Lilly project staff, and selected A&E firm to complete the detailed design of the assigned areas employing QbD and QRM principals and ensuring the integration of Global Quality System requirements into the design, verification, validation and start up.
  • Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance).

Matching Summary

Match Score: 85

Eli Lilly is seeking a Scientist for their Quality Assurance team in the new Parenteral, Device, and Packaging Assembly Facility in Research Triangle Park, North Carolina. The ideal candidate will have extensive experience in parenteral manufacturing quality assurance, particularly in cGMP compliance, and will play a crucial role in the design and startup phases of the facility.

Salary

$65,250 - $169,400; Bonus/Equity: Company bonus; Benefits: Comprehensive benefit program

Skills & Requirements

Must-have

  • cGMP expert
  • Parenteral manufacturing quality
  • Verification and validation oversight
  • Quality oversight of verification activities
  • QbD and QRM principles

Nice-to-have

  • Strong technical aptitude
  • Foster a strong quality culture
  • Build technical capability
  • Global parenteral platforms experience
  • Barrier or isolator technologies

Key Requirements

  • At least 5 years of quality knowledge
  • Previous experience with C&Q / Verification and Validation oversight
  • Bachelors or equivalent degree in a scientific field

Work Rights

Not specified

Tailored Resume

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