QA Documentation Specialist I - PQS/Veeva, Onsite

TekWissen ®; Vacaville (CA); On-site; USD 27,552 - 34,440; Part time

Job summary

A strategic workforce management provider is seeking a QA Documentation Specialist I to support quality system management through document control activities. The position requires 1–3 years of experience in the pharmaceutical industry, proficiency in Veeva Quality Document Management System, and strong collaboration skills. The role will focus on ensuring compliance with regulations, maintaining document quality, and executing PQS integration in Vacaville, CA. This position offers a pay range of $20 to $25 per hour.

Qualifications

• 1–3 years of experience in Quality within the pharmaceutical or biopharmaceutical industry.
• Supplier quality experience preferred.
• Strong technical writing skills.

Responsibilities

• Support implementation, execution, and maintenance of PQS integration.
• Collaborate to manage document gating and coordinate change processes.
• Initiate and manage documents in Veeva Quality Docs.
• Ensure compliance with cGMP and global quality requirements.

Skills

Collaboration within cross-functional teams

Experience with Veeva Quality Document Management System

Technical writing

Tools

Veeva

Microsoft Teams

Job description

A strategic workforce management provider is seeking a QA Documentation Specialist I to support quality system management through document control activities. The position requires 1–3 years of experience in the pharmaceutical industry, proficiency in Veeva Quality Document Management System, and strong collaboration skills. The role will focus on ensuring compliance with regulations, maintaining document quality, and executing PQS integration in Vacaville, CA. This position offers a pay range of $20 to $25 per hour.