Description:
We are seeking a Technical Writer with a strong scientific background to support documentation and compliance in a regulated biotech/pharma lab environment. Key Responsibilities:Write and revise SOPs, protocols, technical reports, CMC sections, and regulatory documents Author and manage deviations, investigations, and change controls Work with Empower, LIMS, TrackWise, Veeva, and SAP systems Coordinate with vendors, manage testing shipments, and process invoices Support GMP/GLP compliance and st
Aug 6, 2025;
from:
dice.com