Sr. Quality Specialist, GxP Document Control

Position Overview

Reporting to the Sr. Director, GxP Quality Management Systems, the Senior QA Specialist, GxP Document Control and Quality Systems is responsible for supporting the administration, organization, and continuous improvement of the Quality Management System (QMS) at Bicara Therapeutics. This role serves as a key resource for document control, quality systems coordination, audit scheduling and tracking, and general QA operational support. Core to this work is ensuring quality documentation is accurate, organized, inspection‑ready, and maintained in accordance with company procedures and applicable GxP requirements.

This role is based in Boston with a hybrid schedule (three days onsite per week); however, a remote schedule would be considered.

Responsibilities

• Lead day‑to‑day document control activities within the electronic QMS, including development, formatting, routing, review, approval, issuance, revision, archival, and re...