PLS Technical Writer

The PLS Technical Writer is responsible for authoring, coordinating, and maintaining Quality Management System (QMS) documentation and quality records to support compliant GMP operations within a regulated contract testing laboratory. This role involves collaborating with cross-functional teams to develop, revise, and manage controlled documentation, including investigations, deviations, CAPAs, and SOPs, ensuring compliance with cGMP regulations and data integrity requirements. The position requires translating complex laboratory and operational data into clear, scientifically sound technical documentation while supporting audit readiness and continuous improvement initiatives.