The successful candidate will contribute to the advancement of our product pipeline by performing QA batch record review, label review and verifications, document archival of records, and other assigned tasks
Job Summary
The successful candidate will contribute to the advancement of our product pipeline by performing QA batch record review, label review and verifications, document archival of records, and other assigned tasks.
Responsibilities include, but are not limited to: Reviews routine manufacturing batch documentation and quality control data for in-process and finished product to support disposition and lot closure.
The annual base pay for this position ranges from $ 65,556.80 - $98,335.20.
Matching Summary
The successful candidate will contribute to the advancement of our product pipeline by performing QA batch record review, label review and verifications, document archival of records, and other assigned tasks.
Salary
Base: $65,556.80 - $98,335.20; Bonus/Equity: short-term incentive bonus opportunity, equity-based long-term incentive program; Benefits: qualified retirement program [401(k) plan], paid vacation and holidays, paid leaves, health benefits (medical, prescription drug, dental, and vision)
Skills & Requirements
Must-have
QA batch record review
label review and verifications
document archival
cell therapy quality assurance
manufacturing batch documentation review
quality control data review
Nice-to-have
organizational, prioritization, and time management
collaborate, work, and communicate effectively
attention to detail and quick learning
knowledge of cell culture techniques
work in a self-guided manner
Key Requirements
BA/BS in Biology, Chemistry, Microbiology, Engineering, or related field
Associate’s degree with up to 2 years of relevant experience
High School diploma with up to 4 years of relevant experience
Must be able to work on multiple projects simultaneously
Flexibility of occasionally working in weekend or holidays