Demo

Document Specialist I, QA

Kashiv BioSciences LLC
Piscataway, NJ Full Time
POSTED ON 1/22/2025
AVAILABLE BEFORE 4/21/2025

Job Type

Full-time

Description

Position Summary

The 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 & Responsibilities

  • Issue 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.
  • Provided weekly status updates to upper management for all pending document reviews in the Electronic Document System.
  • Provides Help Desk support to users of the documentation system. This includes creation and monitoring of incident tickets requiring help desk support from the Electronic Document System Administrator.
  • Assists 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.

Requirements

PREREQUISITES : 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. :

  • MasterControlâ„¢ 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 : No

    This 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.

    If your compensation planning software is too rigid to deploy winning incentive strategies, it’s time to find an adaptable solution. Compensation Planning
    Enhance your organization's compensation strategy with salary data sets that HR and team managers can use to pay your staff right. Surveys & Data Sets

    What is the career path for a Document Specialist I, QA?

    Sign up to receive alerts about other jobs on the Document Specialist I, QA career path by checking the boxes next to the positions that interest you.
    Income Estimation: 
    $63,800 - $85,561
    Income Estimation: 
    $91,786 - $137,269
    Income Estimation: 
    $63,800 - $85,561
    Income Estimation: 
    $91,786 - $137,269
    Income Estimation: 
    $58,384 - $80,655
    Income Estimation: 
    $66,424 - $91,471
    Income Estimation: 
    $66,424 - $91,471
    Income Estimation: 
    $84,144 - $115,539
    Income Estimation: 
    $84,144 - $115,539
    Income Estimation: 
    $100,253 - $149,579
    View Core, Job Family, and Industry Job Skills and Competency Data for more than 15,000 Job Titles Skills Library

    Job openings at Kashiv BioSciences LLC

    Kashiv BioSciences LLC
    Hired Organization Address Piscataway, NJ Full Time
    Job Type Full-time Description Requirements Essential Duties & Responsibilities : Responsible to support manufacturing t...
    Kashiv BioSciences LLC
    Hired Organization Address Chicago, IL Full Time
    Apply Job Type Full-time, Contract Description The Manufacturing Supervisor (DS), is a regular employee in a full-time n...
    Kashiv BioSciences LLC
    Hired Organization Address Chicago, IL Full Time
    Description: The Manufacturing Associate II (DS), is a regular employee in a full-time non-exempt position at Kashiv Bio...
    Kashiv BioSciences LLC
    Hired Organization Address Piscataway, NJ Full Time
    Essential Duties & Responsibilities Create revenue generation opportunities through diverse business development avenues...

    Not the job you're looking for? Here are some other Document Specialist I, QA jobs in the Piscataway, NJ area that may be a better fit.

    VoIP Specialist

    Document Solutions LLC, Lakewood, NJ

    QA Specialist

    MAESTRI D'ITALIA INC, Lakewood, NJ

    AI Assistant is available now!

    Feel free to start your new journey!