Dhara A

Senior Lifescience Recruiter at VIVOS Professional Services, LLC
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Contact Information
us****@****om
(386) 825-5501
Location
Jersey City, New Jersey, United States, JE

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Credentials

  • ISO Registration Process
    IBM
    Mar, 2013
    - Nov, 2024

Experience

    • United States
    • Staffing and Recruiting
    • 1 - 100 Employee
    • Senior Lifescience Recruiter
      • Apr 2020 - Present

    • United States
    • IT Services and IT Consulting
    • 1 - 100 Employee
    • Technical Recruiter
      • May 2017 - Apr 2020

    • QMS and ISO coordinator
      • Sep 2015 - Apr 2017

      Drive and monitor Audits of the company according to the Audit Program and QMS Procedure, o Follow up of planning of each audit, including: notification of auditees, analysis, recommendation and submittal for approval of the Audit Plan, ensure that Audit Plan has been dispatched to auditees, providing assistance to auditors during the steps of preparation, o Interfacing between auditors and auditees. Act as a facilitator of audits. o Ensure the completion of the audit. Receive the signed audit reports within reasonable due time. o Ensure that conclusions of the audit are understood by the auditees.  Manage and monitor nonconformities with respect to the QMS Procedure. o Ensure that nonconformities are correctly entered into GAINNS and all section are fulfilled, and make sure relevant persons are notified on occurrence of nonconformance, o Follow the responsiveness of process owners on nonconformities treatment.  Follow up the Corrective and Preventive actions. o Make sure quality incidents are recorded into GAINNS, o Ensure investigations are conducted and root causes are identified, o Ensure Corrective Actions/Preventive Actions are established and recorded into GAINNS o Monitor the Corrective/Preventive actions following the QMS Procedures,  Promote Opportunities For Improvement within the organization. o Use the results of Audit to identify opportunities for improvement for all QMS processes. o Monitor Opportunities For Improvement in GAINNS Show less

    • India
    • Biotechnology
    • 700 & Above Employee
    • Quality Assurance Specialist
      • Nov 2013 - Nov 2014

    • QA/RA Senior Executive- Risk Assessment and Mitigation
      • Nov 2012 - Nov 2014

      QA Responsibilities:CGMP Requirements of the companyRisk analysis of the new procedures and equipments introduced in the companyInspect and apply the CAPA wherever necessaryDocument the Risk Analysis reports for the Annual Review Report.

    • United States
    • Hospitals and Health Care
    • 700 & Above Employee
    • Clinical Compliance Co-op
      • Jul 2011 - Dec 2011

    • Quality Assurance/Regulatory Affairs Executive
      • Apr 2009 - Dec 2010

Education

  • Northeastern University
    Masters in Regulatory Affairs, Regulatory affairs Drugs Biologics and Medical Devices
    2011 - 2012
  • Sri Indu Institute of Pharmacy JNTU
    BACHELORS IN PHARMACY, Pharmacy
    2006 - 2010
  • DAV
    matriculation

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