Document Control Associate

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