Technical Writer at Bristol Myers Squibb · New Brunswick, NJ · Joined
BS
Technical Writer
Bristol Myers Squibb · New Brunswick, NJ · Just now · 0 applicants
NewHybridFull-timeMiddle
Pay
Pay not listed
Workplace
Hybrid
Job type
Full-time
Level
Middle
Source: jobright · Posted by joined-scrapper
About the role
Bristol Myers Squibb is seeking a Technical Writer to author and coordinate CMC regulatory submission content for its Cell Therapy portfolio, collaborating with cross-functional teams to meet filing deadlines.
What you’ll do
Author and coordinate regulatory submission content
Manage submission timelines and document processes
Collaborate with cross-functional technical and regulatory teams
Support regulatory strategy for CMC documentation
What you’ll need
Bachelor's degree in Biology or related discipline with 2+ years experience
Cell therapy CMC experience
Familiarity with eCTD structure
Outstanding verbal and written communication skills
Proficiency in Microsoft Office (Word, Excel, SharePoint, PPT)
Experience in biotech/pharma end-to-end product development
Original job description
Bristol Myers Squibb is hiring a Technical Writer to deliver CMC documentation supporting regulatory strategy for its Cell Therapy clinical portfolio, from early development through registrational applications. The role authors and coordinates regulatory submission content, manages submission timelines and document processes, and collaborates with…