Careers

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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