Document Specialist I, QA - Kashiv BioSciences LLC : Job Details

DescriptionPosition SummaryThe Documentation Specialist I is a regular employee in a full-time position at Kashiv BioSciences, LLC, in Piscataway, NJ. The employee is responsible for review, issuance, control of procedures, forms, test methods and reconciliation throughout the organization. The Documentation Specialist will assist on maintaining the employees training files and training curriculum, to ensure employees remain current in assigned training.Essential Duties & ResponsibilitiesIssue and control, but not limited to, Master Batch Records, Controlled Forms, Logbooks, Test methods, Protocols and Reports.Issue and route Documents Change Request (DCRs) in the Electronic Document System.Assist on scanning all batch records, validation documentation, calibration information, and supporting documentation and post on the company portal as needed.Perform audit of issued Controlled Forms, Master Batch Records, and Logbooks to finalize reconciliation and ensure timely return of documents for final archival.Receive documentation and ensure documents are properly archived easily retrievable.Ensure documents are properly formatted.Responsible for template management to ensure harmonization among documents within the organization.Track and trend lead-times for Document Change Requests.Provide weekly status updates to upper management for all pending document reviews in the Electronic Document System.Provide Help Desk support to users of the documentation system, including creation and monitoring of incident tickets requiring help desk support from the Electronic Document System Administrator.Assist change originators in coordination of document releases.Responsible for identifying and implementing efficiency improvements to the overall document control process.Assist the training team by tracking and trending training files to complete training modules.Upload pdf versions of procedures to corporate portal.Manage a broad spectrum of projects to support the needs of Quality Management.Perform other duties and responsibilities as delegated by Quality Management.RequirementsPREREQUISITES:Education:A bachelor's degree from a four-year university/college in life science, computer science, or other related field; or 5 + years of experience in a training and/or document control capacity, preferably in cGMP regulated industry.Experience:Previous experience working in a training capacity is desired. Experience commensurate with position level.Previous experience with electronic document management systems is desired. Experience commensurate with position level.Previous work in a cGMP industry is desired.Certifications, Licenses, etc.:MasterControl Electronic Document Management System Operation certification is preferred.Work Environment & Physical Demands:General work environment and physical demands as required to successfully perform the essential functions of this job. Ability to work flexible hours as needed. Ability to work under pressure and meet deadlines.Supervisory Responsibility, if any: NoThis position description is not a complete list of all responsibilities, duties or skill required for the job and is subject to review and change at any time, with or without notice, in accordance with the needs of the organization.#J-18808-Ljbffr