Quality Documentation Specialist I (Veeva & cGMP)

SGS Consulting; Sacramento (CA); On-site; USD 70,000 - 95,000; Full time

Job summary

SGS Consulting in Vacaville, CA, seeks a Quality professional to support PQS integration and management of Quality Documents within Veeva. This on-site role requires 1–3 years of Quality experience in pharma or biopharma, preferably in supplier quality.

Knowledge of Veeva QDM and strong technical writing skills are a plus. You will collaborate with cross-functional teams to ensure documentation workflows, change control, and regulatory compliance while maintaining readiness for inspections at

Qualifications

• Experience collaborating within a cross-functional team in a regulated biopharma setting.
• On-site presence at Vacaville site is required.
• Preferred experience with Veeva Quality Docs and Microsoft Teams; technical writing is a plus.

Responsibilities

• Support PQS integration by assisting in workflows and approvals at the Vacaville site.
• Support PQS integration by coordinating document change processes with gating and QA teams.
• Initiate and manage documents in Veeva Quality Docs and format/edit control documents.
• Track and log requests for source documents and ensure compliance with cGMP and global requirements.
• Maintain high inspection readiness at all times through disciplined document control.

Skills

Collaboration

On-site presence

Technical writing experience

Tools

Veeva Quality Document Management System

Microsoft Teams

Job description

SGS Consulting in Vacaville, CA, seeks a Quality professional to support PQS integration and management of Quality Documents within Veeva. This on-site role requires 1–3 years of Quality experience in pharma or biopharma, preferably in supplier quality.

Knowledge of Veeva QDM and strong technical writing skills are a plus. You will collaborate with cross-functional teams to ensure documentation workflows, change control, and regulatory compliance while maintaining readiness for inspections at