Valeant Pharmaceuticals

  • Document Control Quality Analyst II

    Job Location US-SC-Greenville
    Job ID
    10702
    Pos. Category
    Manufacturing
    Pos. Type
    Full Time
  • Overview

    The QA Documentation Analyst is responsible for processing all Greenville Standard Operating Procedures (SOPs) and for the daily management of the SOP program.   This position is also responsible for the tracking and management of Quality Controlled Documents. Routine contact with all organization levels and departments is required through verbal and written communication.  This position will also routinely provide administrative support for External audits (FDA, ISO, Global, etc) and to the Quality Systems group, when needed.

    Responsibilities

    Process Greenville SOPs in GDMS to include reviewing, routing, promotion of effective documents, copying and distributing copies. 

    Maintain the Annual SOP Review Process, which includes sending monthly notifications of SOPs to be reviewed, issuing periodic SOP status reminders, completing monthly reports. Manages process for review of Regional document updates to ensure local changes are made as necessary to maintain compliance with the Regional Quality System.

    Provide administrative support for external audits and as needed for the Quality Systems group.

    The QA Documentation Analyst may also serve as primary support for CQMS administrative changes, as well as supporting the administration of the records management process. 

     

    SCOPE OF POSITION:

    The QA Documentation Analyst is responsible for processing all Greenville Standard Operating Procedures (SOPs) and for the daily management of the SOP program.  

    This position is also responsible for the tracking and management of Quality Controlled Documents Routine contact with all organization levels and departments is required through verbal and written communication. 

    This position will also routinely provide administrative support for External audits (FDA, ISO, Global, etc) and to the Quality Systems group, when needed.

     

    KEY RELATIONSHIPS:

    All levels and departments internal to the organization. 

     

    HOURS:  Monday - Friday - 8:00am - 4:30pm 

     

     

     

    Qualifications

    Education:  High School Diploma/ GED required.

     

    Experience: 2-3 years of prior office and/or computer (Microsoft Office) experience required. Experience in a GMP regulated environment is preferred.

     

    Preferred Skills: Well organized with the ability to multi-task and shift priorities as needed to meet customer demands.  Demonstrated proficiency in Microsoft Office to include use of Excel spreadsheets, Microsoft Word, and ACCESS database. 

    Knowledge and experience with the Visio program is preferred. 

    Demonstrated proficiency in the use of email.

    Be Aware of Recruiting Fraud

    Valeant Pharmaceuticals International, Inc. is committed to leveraging the talent of a diverse workforce to create great opportunities for our business and our people. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.

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