×
Register Here to Apply for Jobs or Post Jobs. X
More jobs:

QA Documentation Specialist

Job in Vacaville, Solano County, California, 95688, USA
Listing for: TekWissen ®
Full Time position
Listed on 2026-01-12
Job specializations:
  • Quality Assurance - QA/QC
    Data Analyst
  • Healthcare
Salary/Wage Range or Industry Benchmark: 20 - 25 USD Hourly USD 20.00 25.00 HOUR
Job Description & How to Apply Below
Position: QA Documentation Specialist I

Job Title:

QA Documentation Specialist I

Duration: 6 Months

Job Type: Contract

Work Type: Onsite

Shift: Monday to Friday from 08:00 AM to 05:00 PM

Pay Range: $20 to $25 per hour

Overview

Tek Wissen is a global workforce management provider headquartered in Ann Arbor, Michigan that offers strategic talent solutions to our clients worldwide. Our client is a leading biotechnology company that combines technological insight with world‑class manufacturing, scientific expertise, and process excellence and helps their customers to deliver new and innovative medicines that help treat a wide range of diseases. Our client specializes in pharmaceutical ingredients, bioscience, biopharmaceuticals, custom manufacturing, biotechnology, life science ingredients, nutrition, microbial control, agriculture, materials science, personal care, and cell and gene therapy.

Summary

We are looking for a motivated and detail‑oriented Quality Systems Support Specialist to join our Vacaville, CA team. The role focuses on supporting Quality System Management through document control activities and PQS integration, ensuring full compliance with cGMP and global regulatory requirements.

Responsibilities
  • Support implementation, execution, and maintenance of PQS integration and Quality Documents in Veeva for the Vacaville site.
  • Collaborate with the Quality Document Control group to complete workflows, manage document gating, and coordinate document change processes to minimize operational impact.
  • Initiate and manage documents in Veeva Quality Docs.
  • Format and edit controlled documents.
  • Track and log source document requests.
  • Ensure all activities comply with cGMP and global quality requirements.
  • Maintain a high level of inspection readiness at all times.
Required Skills
  • 1–3 years of experience in Quality within the pharmaceutical or biopharmaceutical industry (supplier quality experience preferred).
  • Strong ability to collaborate within diverse, cross‑functional teams.
  • Experience with Veeva Quality Document Management System and Microsoft Teams.
  • Technical writing experience.

Tek Wissen® Group is an equal opportunity employer supporting workforce diversity.

#J-18808-Ljbffr
To View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
 
 
 
Search for further Jobs Here:
(Try combinations for better Results! Or enter less keywords for broader Results)
Location
Increase/decrease your Search Radius (miles)

Job Posting Language
Employment Category
Education (minimum level)
Filters
Education Level
Experience Level (years)
Posted in last:
Salary