Base: $65,250 - $169,400; bonus: eligible for comp...
Not specified (likely on-site or hybrid based on typical industry standards).
5+ years gmp quality control laboratory experience
Api or finished product manufacturing knowledge
Experience with method validation and transfer
Eli Lilly is seeking an Associate for their Quality Assurance team focusing on Quality Control activities related to Active Pharmaceutical Ingredients (API). The ideal candidate will have a background in GMP Quality Control with at least five years of experience and a strong understanding of regulatory requirements
Job Summary
This role serves as a liaison between Contract Manufacturing organizations and Eli Lilly to ensure quality compliance.
The position requires providing quality oversight of QC activities, method validations, and stability programs in accordance with cGMPs.
Eli Lilly offers a comprehensive benefit program including medical, dental, vision, 401(k), and wellness benefits.
Matching Summary
Match Score: 85
Eli Lilly is seeking an Associate for their Quality Assurance team focusing on Quality Control activities related to Active Pharmaceutical Ingredients (API). The ideal candidate will have a background in GMP Quality Control with at least five years of experience and a strong understanding of regulatory requirements.
Salary
Base: $65,250 - $169,400; Bonus: Eligible for company bonus based on performance; Benefits: Comprehensive program including 401(k), medical, dental, vision, and wellness
Skills & Requirements
Must-have
5+ years GMP Quality Control Laboratory experience
API or finished product manufacturing knowledge
Experience with method validation and transfer
Knowledge of cGMPs and regulatory commitments
Ability to review analytical procedures and deviations
Nice-to-have
Small molecule testing experience
Root cause analysis skills
Statistical application skills
Coaching and mentoring abilities
Strong written and verbal communication
Key Requirements
BS in Pharmacy, Chemistry, Biological Sciences, or Life Sciences
5+ years of GMP Quality Control Laboratory knowledge
Authorized to work in the United States on a full-time basis
Work Rights
Must be authorized to work in the US on a full-time basis