Document Control Associate

Document Control Associate You will be part of a growing lab support group and part of an agile team to create a strong, collaborative culture. Prefer 0-2 years of previous document control experience, preferably in a regulated industry. 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
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