Description: Manufacturing Senior Technical Writers work cross-functionally with Manufacturing, MS&T, and Quality groups to lead MO deviation investigations, and author/revise GMP documentation to support clinical and commercial lot release for 2 CAR T products. The Senior Technical Writer will also …read more

Key Responsibilities and Major Duties: Write and revise standard operating procedures (SOPs) for GMP Analytical and Microbiology laboratory operation and instruments. Ability to interview cross functional subject matter experts and translate their description into actionable instructions- Work Instructions, Job Aids …read more