Shabbir Shaikh

To grow in a conducive environment exploiting my domain and potential to the fullest extent to attain the ultimate goal of the organization where I can prove myself and nevertheless to be a good team facilitator.

Married.

Muslim

▪ KRKA(UK)

▪ WOCKHARDT

▪ RANBAXY

▪ MEXICO

▪ ANVISA (Brazil)

▪ Lupin

▪ Glenmark

▪ Egis

▪ USFDA

▪ Health Canada

▪ TGA

• ACG Pam AF 25T Capsule filling machine
• Glatt autocoater
• Autocoater 12",18"24"and 36"pan size Make (Kevin)
• Gea Compression machine
• Sejong autocoater
• Ganson autocoater
• FBP(Gea)
• HSMG (Gea)
• Blender Bin (Gea)
• Fabtech Isolator
• Semi-automatic tablet tester
• Friability tester
• Cage bin blender
• Vibrosifter
• Tablet inspection belt
• Capsule inspection belt

• Look after Granulation, Compression, Coating and Capsule filling activities.
• Responsible for planning day to day activities in Production Department.
• Responsible for monitoring output of Production.
• Preparation of Daily Production Report.
• To take charge of operations from previous shift’s Chemist/Officer and give charge of operations to next shift’s Chemist/Officer.
• Allocating & managing the men power in Tablet Production Department as & when required.
• Performing I.P.Q.C. (In Process Quality Control) during the manufacturing of Tablets.
• Compliance of the requirement of cGMP.
• Co-ordination with Q.A., Q.C., Maintenance Department.
• To maintain safety, efficacy, quality and enhance quality during all Pharmaceutical operations.
• To manufacture all products with the compliance of respective Batch Formula Record.
• To ensure final completion of BMRs, Log Books & all other records on line and transfer to Q.A.
• To train the Workers & Operators regarding the SOPs on job training & evaluation of the same.
• Review of Standard Operation Procedures (SOPs) for the activities of Production Department.
• Preparation of SOP
• Initiating deviation, change control as per discrepancy observed during manufacturing process.
• Initiate the investigation of OOS and OOT.
• Maintaining of regular shop floor documentation.
• Maintaining and completion of BMR.
• Training of personnel and attending to their grievances.
• Indenting of various spares parts required for the department.
• To complete production schedule as per accepted plan with Quality, Productivity & Optimum utilization of resources.
• Review of draft copy of BMR
• Responsibility for the completion of daily output and adjusts the manpower as per the requirement.
• Control & maintaining daily documentation related to batch manufacturing, area cleaning, calibration & validation.
• Check the Schedule of preventive maintenance of all equipments located in dept.
• Reduction of production overheads by minimizing rejection at various stages & cost controlling whenever possible.
• Also involved in Dispensing of raw materials i.e ( Excipient and API) and sifting of Excipient and API
• Handling of DMS and Amplelogic and for SOP preparation,initiation of change control, deviation and other QMS activities.
• Software handled for SOP preparation as Docuzen and Eduzen for training.

GawaliShilpaShilpaEduzenNatioShabbir Khudbuddin>Shaikh

English, Hindi & Marathi

Learning new things, making new friends, Playing Cricket, Carom, Listening Music

• Certificate for appreciation for " Best discipline in Production OSD Department for the Year 2021.