BestJobs - Jobs - QC Supervisor

    Description


  • • Responsible for the overall Quality Control Program of the Manufacturing which includes scope, frequency, methods of sampling and testing.
    • Prepare on time Quality Control report to summarize test results and coordinate to concerned department for necessary actions.
    • Conducts analysis of raw materials, intermediates, bulk products and finished products as per documented analytical procedures.
    • Responsible for providing testing disposition of raw and packaging materials, in-process samples, finished products according to defined specification within the agreed lead time.
    • Maintain the QC Laboratory to ensure continuous support to the operations and compliance to Good Laboratory Practices (GLP) and reviews its capacity based on current needs.
    • Familiarity with Standard Operating Procedures and compliance with the Good Laboratory Practices, Good Documentation Practices and Current Good Manufacturing Practices.
    • Participate in appropriate technical seminars, conferences, workshops to develop competency and familiarity with the latest development on the field of chemical testing.
    • Provide statistical input into development of plans and justification of results using statistical and quality risk management tools (design of experiment, failure mode and effect analysis, hazard analysis, fault tree analysis).
    • Assist with test method modifications, development and validation of new analytical method.
    • Responsible to interpret complex analytical results, troubleshoot and develop complicated methods and techniques, complete development, application and validation of work (protocol drafting, data collection and preparation of report).
    • Recognize results that deviate from established standards, specifications and trends and independently recommend appropriate actions. Perform testing necessary to investigate out-of-specification (OOS) test results. Complete OOS reports including corrective and preventive actions independently.
    • Support and monitor testing of new formulations and stability products.
    • Review and approve testing documentation of other analysts. Prepare analytical reports and certificate of Analysis.
    • Use strong analytical, problem solving and independent decision making skills.
    • Conduct in-house calibration of instruments.
    • Perform regular potability test of process and drinking water to ensure compliance to standards.
    • Train and develop other Technical Services Department associates.
    • Prepare and revise Standard Operating Procedures by biannual review. Update current methods as necessary using the change control system.
    • Organize and schedule of work load for team members.
    • Enforce safety procédures and report safety incidences.
    • Plan, oversee and implement the departmental objectives in meeting the company’s strategic plans.
    • Alternate to sign the final release of the finished product in the absence of Plant Manager and QA Supervisor.
    • Conduct raw material audits.
    • Coordinates inter-departmental quality activities.
    • Perform other duties that may be assigned from time to time.

  • Requirements

  • Minimum education level: Bachelor´s Degree
  • Years of experience: 2
  • Language(s): Tagalog ,English
  • Knowledge: Microsoft Excel, Microsoft Outlook, Microsoft Word
  • Availability for travel: No
  • Availability for change of residence: No

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Job summary

  • QC Supervisor

  • Cavite, Calabarzon

  • Company

    Philippine United Pharma Corp.
  • Work type

    Permanent contract

  • Type of contract

    Full Time

  • Salary

    ₱ 25,000.00 monthly

  • Apply