Document Control Supervisor

Document Control Supervisor

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


Schedules and oversees the implementation of new document control projects. Authors and reviews documents regarding document control procedures. Maintains training requirements for self and all direct reports. Schedules and manages project work for document control direct reports. Supports QA Director/Manager during client audits. Works with quality group to ensure compliance for all document control duties and project implementation. Maintains adherence to QCL SOPs. Compliance with cGMPs and company policies and procedures. Trains and mentors all direct reports. Communicates daily with direct reports regarding project status and daily workload. Communicates with Document Control Manager to maintain current and implement new processes. Maintains strict client confidentiality. Maintains and troubleshoots problems with company databases. Performs all document control associate duties as needed. Performs other related duties, as required.



Bachelor’s Degree or its equivalent and 0-2 years of experience in the pharmaceutical field or in a related area. 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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