QC Manager

Quality Control Manager

Cipla, Rabat-Salé-Kénitra, Morocco (On-site)

Key Accountabilities:

• Supervise and follow up analytical analysis at QC lab
• Review the SOP, check and approve all QC documentation and give guidance according to Cipla Corporate SOP, Pharmacopea (USP, Eur., British).
• Coordinate daily, weekly and monthly planning to ensure adherence with the objectives
• Approve and interpret the results of the tests performed at the QC lab
• Initiate and conduct investigations in case of 00S/OOT results
• Recommend and take corrective action in compliance with quality audits, issues
• Follow the monitoring of stocks and needs for quality control and analysis work (material, reagents, columns, reference substances, WS etc.)
• Plans, monitors and approves the qualification of laboratory instrumental/apparatus and its good working condition according to the requirements of the pharmacopoeia and according to the suppliers
• Manage QC documentation (registers, log-book, SOP, equipment qualification files, etc.)
• Plan the activities of the Department of Quality Control (control planning) according to the objectives
• Participate in the establishment of the QC's operating budget
• Participates in the establishment of the training plan of his team
• Ensure the application the application of traceability, GMP, BPL and HSE rules
• Participate in the approval and validation of suppliers for analytical orders
• Participates in all the tasks necessary for the good functioning of the QC
• Ensure the application of all SOP and the respect of deadlines analysis

Qualification & Experience:

• PhD/Master degree in chemistry, physics or biology
• 6 years worth of experience in pharma industries in similar post