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.
Grifols Egypt for plasma derivatives is a joint-venture (JV) company between the Egyptian Government, through the National Service Projects Organization (NSPO) and Grifols, the global leader in plasma medicines with more than 110 years of contribution to improving the health and well-being of people.
This joint venture is the first of its kind in the plasma industry and the first-ever Egyptian source member of the Plasma Protein Therapeutics Association (PPTA). GEPD is a groundbreaking global public-private alliance that will benefit the entire region.
GEPD is committed to developing the plasma medicines market and achieving self-sufficiency in these critical therapies, which is crucial for the Egyptian healthcare system.
We are combining the expertise of both shareholders to build and operate 20 plasma donation centers throughout Egypt, along with manufacturing facilities including fractionation, purification, and fill-and-finish plants with a processing capacity of up to 1 million liters of plasma annually that can double in the future.
The new manufacturing facility will include a plasma warehouse and a testing laboratory. It will occupy 105,000 square meters strategically located in the administrative capital’s medical city, adjoining various healthcare institutions.
