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QC Supervisor

Hikma Pharmaceuticals
Badr City, Cairo
Posted 2 years ago
38People have clicked1 open position
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Job Details

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Job Description

Job Summary:

Responsible for assisting a team of analysts, officers and/or technicians undertaking quality work. Job holders are involved in a full range of quality section responsibilitiesresponsible for assisting a team of analysts, officers and/or technicians undertaking quality work. Job holders are involved in a full range of quality section responsibilities. 

 

Job Description:

  • Responsible for leading the Quality Control team to ensure compliance with all Corporate and local policies, procedures and regulations, while supervising in a cGMP environment.
  • Schedule laboratory testing and provide resource and instrumentation allocation, conducts laboratory investigations, and implements and monitors corrective actions.
  • Ensure timely testing and notification of any aberrant occurrence to Management that presents potential negative impact to manufactured or marketed product.
  • Monitor and maintain quality programs that provide assurance that test specifications are met for raw materials, finished products, intermediates, stability testing.
  • Work cross functionally to coordinate testing schedules and communications in support of the weekly production activities and ensure QC testing and maintenance activities are completed per requirements.
  • Verify, review and make appropriate changes if needed, to any controlled document(s) pertinent to area of responsibility.
  • Ensure team compliance with all policies, procedures and site/company regulations.
  • Coach and develop the team to High Performance while fostering a culture of team ownership. Recognize and reward performance.
  • Set clear vision by ensuring goals and objectives are aligned with site strategies and managing each team member’s performance management.
  • Provide leadership for employees through effective communication, coaching, training and development and provide solutions for the success of the team.
  • Conduct daily Huddle board meetings to update employees and track progress.
  • Measure and communicate team progress against individual, team and site goals and Key Performance Indicators (KPI’s).
  • Manage the department overtime (OT) and ensure that all exception reports are completed and submitted as required.
  • Maintain an acceptable level of 5S in the area and promote proper maintenance and cleanliness of the department areas of responsibility.
  • Assure compliance with department training and qualification.

Job Requirements

Education:

  • Bachelor level degree required, in a science or pharmaceutical sciences.

Experience:

  • From 6: 8 years of experience in a cGMP regulated environment, leadership experience required.

Skills/Competencies:

  • Proficiency in cGMP laboratory testing and major laboratory instrumentation.
  • Ability to interpret laboratory data and make sound compliance decisions based on such interpretations.
  • Excellent communication and interpersonal skills.
  • Excellent decision making, problem solving and analytical skills.
  • Detail-oriented with the ability to work under tight deadlines.
  • Preferably (Cairo, Obour, New Cairo, Nasr City, Heliopolis, Badr, Zagazig, Sharqiyah, and 10th of Ramadan) residents.

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