Date Posted:
Salary:
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Job Description

  • Develop and maintain quality system related to QA oversight of manufacturing processes.
  • Ensure product release operates as independent group (of all other operations) and ensures product release complies with documented specifications and regulatory expectations.
  • Ensure QC Operations is compliance with cGMP’s, ISO regulatory requirements and Alcon Quality Manual.
  • Manage deviations and investigations within QC and support manufacturing investigations as required.
  • Manage and control department budget and expenses and ensure adequate resources for full implementation of Quality Control Plans.
  • Develop and implement lens and product cosmetic standard.
  • Implement QA Engineering function to support and improve GMP practices throughout operations.
  • Accountable for HSE and BCM implementation and performance in the respective function. Provide leadership and responsible for other HSE activities that are assigned by Management.
Requirements
  • Minimum B.S. Engineering or Science (e.g. Chemistry, Biology, etc).
  • 5 years of experience in the medical device or pharmaceutical industry.
  • Thorough knowledge of cGMP/QSR and ISO regulations.
  • Understanding of statistic, LEAN and Six Sigma principles.
  • Strong leadership, people skills and communication.
  • Technical writing background.

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Job Detail

  • Job Id
    2dd93b47ca66bd6c
  • Location
    id
  • Company
  • Type
    Private
  • Employment Status
    Permanent
  • Positions
    Available
  • Career Level
    Experience
  • Gender
    Male/Female

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