Quality Control Supervisor

Job Objective
The Quality Control Supervisor will perform and ensure that the performance of the testing is according to established procedures, as well as, support Laboratory Operations Manager in keeping the SOPs, reports, deviations and other documentation required updated in a timely manner.

Key responsibility
- To ensure the proper receipt and preparation of plasma samples for further testing, as well as the performance of tests following established procedures.
- To participate in the daily testing activities of all testing methods and related procedure and ensure all are properly executed by the QC specialists.
- To ensure all routine screening results interpretation and validation are following the established guidelines and are timely submitted.
- To participate in the elaboration of validation protocols and validation reports for being further reviewed by Laboratory Operations Manager.
- To register and inform of possible deviations occurred during testing and propose measures for improving in the routine analysis.
- To ensure that routine maintenance of equipment involved in sample preparation and testing is performed according to the laboratory plan, as well as the necessary verification for the correct care of the equipment.
- To ensure that the preparation of all the material involved in testing and sample preparation are according to the established procedures.
- To coordinate the team of Quality Control specialist to ensure all tasks are performed in a timely manner.
- To support Laboratory Operations Manager on data retrieving process related to testing laboratory.

Job Requirements 

Academic experience required
Bachelor s Degree in Health-related Sciences.
Knowledge of cGMP requirements preferred.

Professional experience required
Preferably at least 5 years of experience in a similar position with Phrama background, in
environments of Good Manufacturing Practices (GMP).

Computing skills
MS Office knowledge.

Personal skills
Organized and able to manage time effectively.
Ability to work within a highly regulated, labor intensive environment.
Ability to understand, explain, follow, and enforce SOPs and protocols.
Ability to plan, communicate and execute activities for the improvement of overall operations.
Strong integrity and commitment to Quality and Compliance.
Ability to work in groups and with other departments.
Excellent oral and written communication skills to produce clear and concise factual findings.
Ability to identify problems and propose solutions.

Languages
Written and spoken English and Arabic.