Senior Pharmaceutical Documentation Systems Specialist
Listed on 2026-10-06
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Pharmaceutical
Regulatory Compliance Specialist -
Quality Assurance - QA/QC
Regulatory Compliance Specialist, QA Specialist - Analyst/Manager
Afton Scientific seeks an experienced Documentation Systems Specialist III to join its Quality Assurance team in Virginia. You will administer master documents and databases, ensuring accuracy, traceability, and compliance with cGMP and FDA/EU guidelines.
The role requires strong documentation skills, familiarity with GMP-driven systems like Master Control or Veeva, and the ability to collaborate across QA, Operations, and Regulatory functions to support audits, changes, and validations.
Consider building your career as a Senior Pharmaceutical Documentation Systems Specialist at Rippling, Inc.
Our organisation is growing, and we are hiring a Senior Pharmaceutical Documentation Systems Specialist in Charlottesville, VA, United States.
This role is for the Senior Pharmaceutical Documentation Systems Specialist role at Rippling, Inc.
We are seeking a motivated Senior Pharmaceutical Documentation Systems Specialist to join Rippling, Inc. in Charlottesville, VA, United States.
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