tekwissenVacaville, CA
QA Documentation Specialist I
$20 to $25 per hour
Apply →QA Documentation Specialist I
QA Documentation Specialist I
tekwissenVacaville, CA
19 days ago
$20 to $25 per hour
Quality Control AnalystsQuality Control Systems ManagersSoftware Quality Assurance Analysts and Testers
Pharmaceutical Preparation ManufacturingDocument Preparation ServicesBiological Product (except Diagnostic) Manufacturing
Apply for this role →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:
TekWissen 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.
TekWissen® Group is an equal opportunity employer supporting workforce diversity.
Also on the board Same function, level within a rung
Level
Senior
Salary
$20 to $25 per hour
Location
Vacaville, CA
Occupation
Quality Control Analysts
Industry
Pharmaceutical Preparation Manufacturing
Posted
19 days ago