Skills
GMP laboratory testing
Analytical method execution
Quality control documentation
About the Role
Join the Quality Control – Analytics team supporting a growing portfolio of cell and gene therapy (CGT) products, including CAR-T, iPSC, AAV, LVV, and synthetic DNA. As a QC Analyst I, you’ll perform laboratory testing in a fast-paced, GMP-regulated environment while helping ensure data quality and product compliance.
Responsibilities
- Execute laboratory testing to support GMP release and characterization activities
- Assist with the development, qualification, and execution of analytical methods
- Generate, review, and document analytical results according to GMP expectations
- Collaborate with teams across Analytical/Process Development and Manufacturing
- Contribute to maintaining laboratory readiness, equipment use, and quality-focused workflows
Requirements
- Experience performing analytical testing in a regulated laboratory setting (GMP preferred)
- Strong attention to detail and comfort working with technical documentation
- Ability to work effectively in a fast-paced environment and follow established procedures
- Strong teamwork and cross-functional communication skills
Benefits
- Opportunity to support cutting-edge CGT therapies
- Work in a mission-driven, quality-focused GMP environment
- Collaboration with Analytical and Manufacturing partners
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