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Document Control Associate
Job in
Wilmington, New Hanover County, North Carolina, 28412, USA
Listed on 2026-08-29
Listing for:
Quality Chemical Laboratories LLC
Full Time
position Listed on 2026-08-29
Job specializations:
-
Quality Assurance - QA/QC
QA Specialist - Analyst/Manager, Quality Control - QC Analysts/Managers, Regulatory Compliance Specialist
Job Description & How to Apply Below
Maintains document and revision information.
Monitors tasks relating to documents.
Reconciles and updates each SOP manual.
Complies with cGMPs and company policies and procedures.
Supports Document Control Supervisor and QA Director/Manager during client audits.
Scans files/records/data as needed.
Files records as needed.
Prepares files for archive storage.
Performs other related duties, as required. Requirements:
High school diploma or its equivalent and 0-2 years of experience in the pharmaceutical field or in a related area.
Must be proficient in Word, Excel, Access and other Microsoft programs.
Experience with other GMP compliance systems (e.g. Quality management system, change management systems, ERP) is a plus.
Experience in a pharmaceutical company preferred
Excellent interpersonal and communication skills required
Must be able to solve complex business problems and present recommendations to management effectively
Strong verbal and technical writing skills Must be results driven, a quick learner, and a self-starter
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Position Requirements
10+ Years
work experience
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