Mudasser Wali Khan Email & Phone Number

Islamabad, Islāmābād, Pakistan

Islamabad, Islāmābād, Pakistan

Lahore

Jabel Ali, Dubai, United Arab Emirates

• Documentation as per GMP & ISO • QMS• GMP implementation • cGMP• Trainings• OOS,CAPA• Complaint Handling & vendor evaluation • Change control, Deviation Control• Dossiers FOR Registration & Export • Export Documentation & requirements• GDP, GLP• Review of documents • Preparation of plan for Quality audits.• Process validation • Analytical method validations• Calibration of machines and equipments • SHE as per European guidelines• Crises action plan• Fulfill the legal requirements of monitoring agencies & international standards.

United Arab Emirates

Responsibilities:1 SOPs• To check that all working is according to written procedures.• To maintain document control system.• To upgrade SOPs as per International standards.2 Materials• To check inventory level as per requirements.• To check requirement to Supply Chin as per production plan and manage the Quality related issues..• To proceed for the Vender evaluation procedure and approve the vendor.• To release all materials on ERP system.3 New Product Development • To conduct trials for new products.• To develop the testing methods for new products.• Stability Studies.4 Dossiers for MOH and Export registration.• Dossier development for MOH.• Dossier development for export and fulfill all requirements for registration of firm and products.• Equipment Calibration.5 Development and Validation of manufacturing & testing methods.• Process Validation of manufacturing procedures • Analytical methods validation to ensure the repeatability in the results.• APR 6 Safety.• To ensure safe working conditions by implementing safety practices and taking precautionary measures against hazards and accidents.• Rodent & Insect control.7 Training• Training of officers & Managers.• Prepare schedule for training for external & internal speakers.8 Complaints• To investigate the market complaints and to make comprehensive report of findings and to recommend corrective action.• OOS investigation.• Change control system.9 cGMP.• Preparation of monthly report for all of the departments in production / QC to ensure cGMP compliance.• To prepare requirements for the best cGMP compliance.10 Liaison with other Departments.• To maintain good janitorial condition with the help of Admin Department.• To recruit new staff with the liaison of HR department.• Product specifications of new product.• To make all dealings with the problems of marketed products from market staff.• TO EXECUTE ANY WORK GIVEN BY THE MANAGEMENT AT ANY TIME.

32-Km Multan Road Lahore

Responsibilities:Same as in United Pharmaceuticals

Lahore

Worked with the ICI Pakistan and go through all documentation of international standards.

• Microbiological sectionDealt in all test required for microbiological section for IV & eye drops Products.

Testing of Tablets & Liquids

M.Sc., Zoology ( Microbiology), 1St Division

Activities and Societies: Comparing the Events, 3rd Position in final Exam, Managing tours. I have specialized in microbiology and later.

Bachelor Of Science (B.Sc.), Chemistry ,Zoology & Botany

Activities and Societies: Debate team