Sorry, this listing is no longer accepting applications. Don’t worry, we have more awesome opportunities and internships for you.

Document Control Coordinator

Norland Group

Document Control Coordinator

Cincinnati, OH
Full Time
Paid
  • Responsibilities

    12105428-Document Control Coordinator Location: Cincinnati, Ohio 45227 Pay Rate: Up to $20.00/hr Contract Duration: 6 Months Job Title - Document Control Coordinator Location - Cincinnati, Ohio Contract - 6 Months Coordinate the activities of Document Control, including distribution and auditing controlled documents, maintenance of electronic department directories, tracking and reporting on document review progress Work independently to facilitate group activities Manage archival activities for controlled documents, control of label artwork files and verification and validation files Assist with the implementation, management and administration of the department electronic document management system (EDMS) Work with subject matter experts on technical subjects in a positive, collaborative manner to prepare controlled documents which conform to Companys defined format Review and proofread documents for consistency of document format and system concerns Verify and issue production documents and product labels to the manufacturing department Use department databases to track and manage and control issued documents. Assign lot numbers, material part numbers, and various other document tracking numbers Effectively follow SOPs, policies, and GMPs. Provide support for the Quality System during corporate audits, actively participate in department activities Perform audits of company areas and processes to confirm compliance with controlled procedures REQUIREMENTS Education: High School diploma Skills & Abilities: Excellent communication and writing skills. Strong interpersonal skills and ability to work with others in a positive and collaborative manner Demonstrated ability to work accurately, follow instructions/schedules/timelines and handle multiple priorities. Ability to utilize multiple word-processing and database applications including MS Office applications Word, Excel, Access, as well as Adobe PageMaker, Adobe Acrobat, etc. Experience: Minimum of 2 years experience with Quality System Documentation and good documentation practices Knowledge of ISO, FDA and GMP concepts and guidelines We encourage Minorities, Women, Protected Veterans and Disabled individuals to apply for all positions that they may be qualified for. We maintain a drug-free workplace and perform pre-employment substance abuse testing and background checks

  • Industry
    Hospital and Health Care