QA Documentation Specialist I
Aequor JD ·www.aequor.com
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M-F 5x onsite 1st shift (8am - 5pm)
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
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
Frequently asked questions
Who is hiring for the QA Documentation Specialist I role?
Aequor JD is hiring for the QA Documentation Specialist I position, a Shazamme client. Apply directly on the employer's career site.
Where is the QA Documentation Specialist I job located?
The QA Documentation Specialist I role with Aequor JD is based in Vacaville, CA, US.
What does the QA Documentation Specialist I role pay?
Aequor JD lists the QA Documentation Specialist I role at USD 15–26 per hour.
Is the QA Documentation Specialist I role full-time or contract?
This is a full time position at Aequor JD.
What experience level is the QA Documentation Specialist I role?
The QA Documentation Specialist I position is aimed at mid-level candidates.
How do I apply for the QA Documentation Specialist I role at Aequor JD?
Apply directly on Aequor JD's career page via the Apply button on this listing. ZammeJobs links straight through to the employer's ATS — no third-party form, no resume database.