Job Description
Position Title: QA Documentation Specialist I
Work Location: Vacaville, CA 95688
Assignment Duration: 6 months
Work Schedule: M-F 8am - 5pm
Work Arrangement: Onsite
Position Summary: 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: Initiating and management of documents in Veeva Quality Docs.
• Formating and editing of control documents.
• 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.
Qualification & Experience:
• 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.
• Preferred experience with Veeva Quality Document Management System and Microsoft Teams.
• Preferred Technical writing experience.
- For information on benefits, equal opportunity employment, and location-specific applicant notices, click here
At SPECTRAFORCE, we are committed to maintaining a workplace that ensures fair compensation and wage transparency in adherence with all applicable state and local laws. This position’s starting pay is: $ 26.14/hr.