Position Overview
As a Document Control Specialist, you will work maintain controlled documents within the company's quality management system. This position will require expertise in Microsoft Word and Excel as well as PDF automation tools in Adobe Acrobat Professional.
Type: Full time / permanent
Type: onsite (no remote)
Salary: Commensurate with experience
Position Responsibilities
- Facilitate the implementation of the document management system
- Assist the System Administrator in performing the daily functions
- Perform a visual quality check of each document and validate the correctness
- Provide publishing support for company documents
- Assist in managing non-conformance events, deviations, CAPAs in the electronic QMS.
- Document and track Change requests as they are initiated
- Create training courses and manage training for all QMS personnel
Skills, Education and Experience Required
- Associates or bachelor's degree
- Minimum of 3 years of experience in pharmaceutical document control
- Working knowledge of GMPs (21 CFR 210/211, 1271 and 810).
- Experience with Change Control practices/strategies