Supervisor, Qc

1 week ago


مصر, Egypt Hikma Pharmaceuticals PLC Full time

**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.
- 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.

**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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