Find & Apply For Document Control / Management Specialist Jobs in Wilmington, North Carolina

Document Control Associate Quality Chemical Laboratories - 3.1 Wilmington, NC Job Details 8 hours ago Qualifications Microsoft Excel Content creation for technical audiences Technical documentation Word embeddings High school diploma or GED Productivity software Technical writing experience within technology Database software proficiency

Full Job Description Responsibilities:

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