About the job

Are you a talented Technical Writer with expertise in (CMC) documentation within the Biotech industry based in Europe?

I am recruiting for a fast-growing US-based Biotech company on a contract basis as part of an exciting journey in developing life-changing medicines.

Responsibilities;

• Collaborate with cross-functional teams to create, review, and edit CMC documentation, including regulatory submissions, batch records, protocols, and reports.
• Content creation in MAAs, BLAs, INDs and IMPDs
• Work closely with subject matter experts to gather information and clarify technical details

Requirements:

• Proven experience as a Technical Writer within the pharmaceutical industry, specifically in CMC module 3 documentation
• Fluent in English (Mandarin is a bonus)
• Minimum 5 years experience in Biologics

If this sounds like your ideal role, please reach out!

E - Lbroomes@barringtonjames.com