Skip to main content
Tallo logoTallo logo
Apply for this opportunity

This job application is on an outside website. Be sure to review the job posting there to verify it's the same.

QA Documentation Specialist I

Job

TalentBurst, Inc.

Vacaville, CA (In Person)

$49,672 Salary, Full-Time

Posted 4 days ago (Updated 19 hours ago) • Actively hiring

Expires 7/12/2026

Review key factors to help you decide if the role fits your goals.
Pay Growth
?
out of 5
Not enough data
Not enough info to score pay or growth
Job Security
?
out of 5
Not enough data
Calculating job security score...
Total Score
49
out of 100
Average of individual scores

Were these scores useful?

Skill Insights

Compare your current skills to what this opportunity needs—we'll show you what you already have and what could strengthen your application.

Job Description

QA Documentation Specialist
I 3.5 3.5
out of 5 stars Vacaville, CA 95688 $15.69
  • $26.14 an hour
  • Contract TalentBurst, Inc. 65 reviews $15.69
  • $26.14 an hour
  • Contract QA Documentation Specialist I Vacaville, CA 6+ Months with a high possibility of extension M-F 5x onsite 1st shift (8am
  • 5pm)
Description:
We are seeking a highly motivated and experienced Quality Systems Support Specialist to join our team in Vacaville, CA. In this role, you will provide essential support to the Quality System Management process with document control and PQS integration, ensuring compliance with cGMP and global requirements.
Key Responsibilities:
Support the implementation, execution and maintenance of the PQS integration and Quality Documents in Veeva at the Vacaville site. Support PQS integration by working with the Quality Document control group to complete workflows, document gating and coordinate elements of the document change process to ensure minimal disruption to site operations Support Quality Documents by: o Initiating and management of documents in Veeva Quality Docs. o Formating and editing of control documents o Track and log request of source documents Ensure all activities are conducted in compliance with cGMP and global requirements. Strive to maintain the highest level of inspection readiness at all times
Key Requirements:
1-3 years of experience in Quality within the pharmaceutical or biopharmaceutical industry, preferably within a supplier quality function. Ability to effectively collaborate within a diverse, cross-functional team. On-site presence at the Vacaville location is required. Preferred experience with Veeva Quality Document Management System and Microsoft Teams. Preferred Technical writing experience #TB_OTH #ZR Why TalentBurst? At TalentBurst, we deliver more than talent, we deliver outcomes. We partner with you to move quickly and connect you to opportunities aligned with your skills and long term growth. Backed by precision, transparency, and results, we connect top talent with leading organizations through trusted partnerships. We offer competitive compensation and comprehensive benefits, including medical, dental, vision, and retirement options. TalentBurst is an equal opportunity employer committed to an inclusive and diverse workforce.