1. Oncology
2. Attractive package
About Our Client
Our client is a new oncology products manufacturer in Algeria.
Job Description
You will be responsible of the following tasks:
-Supervise the implementation of the Quality Control function plans, and ensure their compliance with client quality system
-Develop the quality control function's work plan; assign work activities, projects and programs, review and evaluate analytical methods and procedures, and directing the quality control activities to serve the QC department objectives.
-Ensure that qualification/validation and maintenance of the QC Laboratory premises and equipment/instruments are appropriately performed
-Develop and maintain quality control procedures by ensuring completion of all tests, studies, reports and investigations in an accurate, effective and timely manner
-Review and evaluate all data generated according to written procedures and recommend on the release or reject of the analyzed items (raw materials, packaging materials, intermediate, bulk and finished products)
-Contribute for evaluation and qualification of vendors of raw materials and packaging materials.
-Inform all involved functions of any rejects and non-conforming results related to raw materials, packaging materials, finished products, and any other area monitored by QC testing
-Lead the execution of investigations on relevant QC issues (OOS/OOT/deviations),verification results and determine corrective and preventive actions as per defined SOPs
-Develop and validate the analytical methods in accordance with the current regulations and apply the latest technical methods
-Validate the analytical test procedures, specification sheets, SOPs (pharmacopoeia and In-house). Review and approve documents related to QC function activities (procedures, protocols, reports, etc.)
-Establish and maintain a tracking and trending system of QC issues (OOS /OOT)
-Conduct performance appraisals for subordinates according to scheduled plans and recommend necessary actions as per the applied practices
-Co-ordinate technical audits of the QC Laboratory to determine the analytical quality systems are yielding the highest quality information and to ensure that the analytical instrumentation is functioning properly and calibration and servicing is as per schedule.
The Successful Applicant
5 years of experience in a related position, of which at least 2 years in supervisory position.
10 years (or more) in a similar position within pharmaceutical company.