Mohammad Mobin Email & Phone Number

• Effectively manage overall activities of Production/Quality Assurance/Quality Control/Ware House/Engineering & procurement/planning functions.• Develop & implement strategies that increase products quality & company profitability.• Organize the plant activities/Task as team work.• Complete compliance of cGMP’s in production/Q.A/Q.C • Analyze the daily production/Q.A/Q.C Operations.• Ensure preventive maintenance program for machines in plant , production & Q.A/Q.C.• Organize cGMP’s training sessions for management/workers/supervisors & senior staff & also giving presentations on pharma related topics.• Ensure validation of area/machine & equipments & manufacturing processes.• Organize technical co-ordination meetings among managers.• Develop the skilled team for production & Q.A / Q.C with concern of management.• Rectify the production difficulties with co-ordination of engineering & other related departments.• Handle regulatory & registration matters (local & export)• FAT / SAT for new machines with co-ordination of Engg. Department.• Ensure proper documentation of new products & the stability studies.• Manage internal & external audit including ISO audit. • Ensure availability of finish stock & in-time deliveries to distributors.• Legal/co-operate matters with ministry of health.• Ensure in-time supplies of Govt. Institutions / Toll stocks & availability of Raw / Packing Material.• Analyze the daily production / Q.C Operations.• Design & Develop product formulations of various dosage forms including oral solids, liquids, and semi-liquid, Injectables (Liquid , Powder & Lyophilized) , Eye / Ear Drops & topical products for branded, generic, Neutraceutical / Herbal products & handle trouble shooting during manufacturing process.• Re-formulate / improve existing products for better quality of products•• To conduct the Brain Storm training programs for all employees.

Effectively managed overall activities of Production / Quality Assurance / Quality Control / Ware House / Engineering functions.• Developed & implemented strategies that increase products quality & company profitability.• Complete compliance of cGMP’s in production / Q.A / Q.C • Ensured the implementation of S.O.P’s in the production / Q.A / Q.C• Analyzed the daily production / Q.A / Q.C Operations.• Managed the quality of all analytical & microbiological systems .• Ensured preventive maintenance program for machines in plant , production & Q.A / Q.C.• Organized cGMP’s training sessions for management /workers / supervisors & senior staff & also giving presentations on pharma related topics.• Ensured validation of area / machine & equipments & manufacturing processes.• Organized technical co-ordination meetings among managers.• Developed the skilled team for production & Q.A / Q.C with concern of management.• Rectified the production difficulties with co-ordination of engineering & other related departments.• Design & Develop product formulations of various dosage forms including oral solids, liquids, and semi-liquid, Injectables , Eye / Ear Drops for branded, generic products. • Handled regulatory / registration matters• FAT / SAT for new machines with co-ordination of Engg. Department.• Ensured proper documentation of new products & the stability studies.• Managed internal & external audit including ISO audit.• Ensured proper maintenance of product’s record.• Ensured availability of finish stock & in-time deliveries to distributors.• Handled Legal/co-operate matters with ministry of health.• Ensured in-time supplies of Govt. Institutions / Toll stocks.• Ensured in-time availability of Raw / Packing Material.• Analyzed the daily production / Q.C Operations.• To design , develop & prepare the S.O.P’s for plant.

• Effectively managed overall activities of Production / Quality Assurance / Quality Control / Ware House / Engineering functions.• Developed & implemented strategies that increase products quality & company profitability.• Complete compliance of cGMP’s in production / Q.A / Q.C • Ensured the implementation of S.O.P’s in the production / Q.A / Q.C• Analyzed the daily production / Q.A / Q.C Operations.• Managed the quality of all analytical & microbiological systems .• Ensured preventive maintenance program for machines in plant , production & Q.A / Q.C.• Organized cGMP’s training sessions for management /workers / supervisors & senior staff & also giving presentations on pharma related topics.• Ensured validation of area / machine & equipments & manufacturing processes.• Organized technical co-ordination meetings among managers.• Developed the skilled team for production & Q.A / Q.C with concern of management.• Rectified the production difficulties with co-ordination of engineering & other related departments.• New products Development (Pharmaceutical & Nutraceutical) of all dosage forms.• Handled regulatory / registration matters• FAT / SAT for new machines with co-ordination of Engg. Department.• Ensured proper documentation of new products & the stability studies.• Managed internal & external audit including ISO audit.

Karachi

•Overall activities of Production/Quality Assurance/Quality Control/Ware House/Planning & procurement & Packing Deptt.•Design & Develop product formulations of various dosage forms including oral solids, liquids, and semi-liquid, Injectables (Liquid,Powder & Lyophilized) , Eye/Ear Drops for branded, generic, OTC products.• To organize the production schedule as per monthly sale forecast.• For complete compliance of cGMP’s in production/Q.A/Q.C • To ensure the implementation of S.O.P’s in the production/Q.A/Q.C• To analyze the daily production/Q.A/Q.C Operations.• To ensure preventive maintenance program for machines in plant , production & Q.A/Q.C.• To organize cGMP’s training program for workers/supervisors & senior staff & also givingpresentations on pharma related topics.• To ensure validation of area/machine & equipments & manufacturing processes.• To organize technical co-ordination meetings among managers.• To develop the skilled team for production & Q.A/Q.C with concern of management.• To rectify the production difficulties with co-ordination of engineering & other related departments.• To co-ordinate with R & D department for the developing of new products of all dosage forms.• Responsible to handle regulatory matters• Responsible of new product registration for Local / Export.• Responsible for FAT / SAT for new machines with co-ordination of Engg. Department.• To ensure proper documentation of new products & the stability studies.• Responsible to manage internal & external audit including ISO audit. • To ensure proper maintenance of product’s record.• To ensure availability of finish stock & in-time deliveries to distributors.• Legal/co-operate matters with regulatory authority.• To ensure in-time supplies of Govt. Institutions / Toll stocks.• To ensure in-time availability of Raw / Packing Material.• To analyze the daily production / Q.C Operations.• To conduct the Brain Storm training programs for all employees.

Total Activities of Production / Quality Control / Ware House / Packing Deptt.• To organize the production schedule as per monthly sale forecast.• For complete compliance of cGMP’s in production / Q.C • To ensure the implementation of S.O.P’s in the production / Q.C• To analyze the daily production / Q.C Operations.• To ensure preventive maintenance program for machines in plant , production & Q.C.• To organize cGMP’s training program for workers / supervisors & senior staff.• To ensure validation of area / machine & equipments & manufacturing processes.• To organize technical co-ordination meetings among managers.• To develop the skilled team for production & Q.C with concern of management.• To rectify the production difficulties with co-ordination of engineering & other related departments.• To co-ordinate with R & D department for the developing of new products.• Responsible to handle regulatory matters• Responsible of new product registration for Local / Export.• Responsible for FAT / SAT for new machines with co-ordination of Engg. Department.• To ensure proper documentation of new products & the stability studies.• Responsible to manage internal & external audit including ISO-9000.• To ensure proper maintenance of product’s record.• To ensure availability of finish stock & in-time deliveries to distributors.• Legal/co-operate matters with ministry of health.• To ensure in-time supplies of Govt. Institutions / Toll stocks.

Following type of work has done by myself & under my Supervision. Documentation : • Preparation of Batch manufacturing record (B.M.R) for Granulation , Compression , Coating , Encapsulation for different products.• Preparation of Standard Operating Procedures (S.O.P’s) for Production Area.• Preparation of S.O.P for Cleaning of Machines, Utensils , Equipments etc.• Preparation of S.O.P for General Cleaning of Production Department.• Preparation of Requisition and Dispensing Operation Sheet.• Preparation of Schedule for formulation.• Designing of Labour Utilization and daily Work Report Sheet.• Designing of In –process control sheet.• Preparation of packing log guide.• Preparation of Proforma for Monthly ‘’ WORK IN PROGRESS’’• Preparation of Proforma for for Quarantine Position.• Preparation of finished Goods Transfer Note to F.P.S. MACHINES : • Preparation of Schedule for Machine overhauling• Setting and uni – coloring scheme for all machines.• Gradual replacement of out dated Machines with modern and speedy machines.• Fabrication and installation of new centralized exhaust system for complete tableting department.• Installation of Heat control and film coating unit for coating section. General :.• Setting and managing of workshop department.• Monthly training programme for junior officers , supervisors and workers in the production department.

M.Phil (Analytical Chemistry) ,• M.Sc (Bio Chemistry), B.Sc (Hons)

Master Of Library & Information Science (Mlis), Biochemistry