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Job Description

Drive and assist on daily operations (Vision Care and Surgical), including validation/qualification activity, continuous improvement, failure investigation & root cause analysis of GMP issues in the manufacturing. Responsible to assist and support failure investigation, root cause analysis, generation and execution of corrective and preventive actions. Responsible to manage and support validation/qualification activities for new product/process/raw material/computer systems qualification. Responsible to ensure compliance, e-compliance and provide guidance plus technical support to quality/manufacturing functions. Responsible to perform product/process and system risk assessment, provide guidance and facilitate risk management reviews. Responsible to lead and drive quality and compliance improvement program and support continuous improvement plan (CIP). Working in accordance with the HSE Manual and documented procedures, and reporting HSE issues to the respective area owners.

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Job Detail

  • Job Id
    d09dbfbcd6a1a376
  • Location
    id
  • Company
  • Type
    Private
  • Employment Status
    Permanent
  • Positions
    Available
  • Career Level
    Experience
  • Gender
    Male/Female

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