Plant Manager CSH North
CSH Pharma Group
Total des années d'expérience :29 years, 2 Mois
Looked after the complete Plant operations at Site as Senior technical Member and Head of Plant Lead all the Technical department heads.
Introduced Effective and Practical documentation system at Plant.
Removed the entire Communication barrier among the Plant and Head office People to speed up the process for timely completion of Projects.
Made a Positive Reputation of the organization in the Market through effective public dealing.
Achieved the Targets in a very short span of time through effective Planning, communication and intelligently utilizing the available resource.
Increased the Firm product range and productivity.
Introduced some very rare Molecule formulation in the Market soon after the Researcher.
Supplied a Product of more than 10 million units to WHO in Pakistan after competing on the basis of Product quality.
Took active Part in Firm Products Export registration in Turkmenistan, Afghanistan, Sri Lanka, and other French speaking African Countries.
Exported Product to Turkmenistan, and Afghanistan.
Prepared All Related import and Export Documents of APIs and Finished Products Consignments (NOCs, COPP, Certificate of origin etc).
Got the registration of Firm from Director General Defense Purchases of Pakistan Army after a successful Inspection of the Premises.
Supplied a Huge amount of different Products to Punjab Government on time Cost effectively.
Developed a liaison with all government specially DRAP, Provincial government and non government department as firm representative.
Got Certification of QMS (ISO9001:2008) as Management Representative.
Developed and supervise directly Supply chain activity through a Team, starting from Approval of Purchase Requisition of Material till Ware Housing and Distribution of Finished Products to Market.
Solved complex problems in formulation, processes, testing and root causes.
Optimized existing formulation and processes to improve product performance, process robustness and safety while reducing costs.
Utilized expertise and knowledge of the practical application of engineering science and technology.
Plan laboratory experiments to confirm feasibility of processes and techniques used in the production of materials having special characteristics.
Prepared reports, manuscripts, proposals and technical manuals for use by other scientists and requestors, including sponsors and customers.
Reviewed processing schedules and production orders concerning inventory requirements, staffing requirements, work procedures and duty assignments, considering budgetary limitations and time constraints.
Oversaw the production process and managed the production schedule.
Reviewed processing schedules and production orders concerning inventory requirements, staffing requirements, work procedures and duty assignments, considering budgetary limitations and time constraints.
Revised the Formulation of Different Product to more efficacious and Cost effective formulation.
Increased the Total No of Manufactured Products from 18 to over 80 after taking the charge as Production Head.
Increased the output by utilizing the idle resource present at Plant.
Increased the Productivity two to three fold through effective utilization of Human, Machine and Material Resources .
Took Active Part in the Implementation of ISO 9002 in 1999 and later on conversion of it to ISO 9001:2000 version.
Took Active Part in the Documentation Revision of the Firm from time to time on Need Basis.
Prepared and approved the Layout of Firm Additional Sections. Develop effective Inventory control system to cater Market demands.
Author protocols for bulk, finished goods and stability testing.
Worked closely with QC staff to develop new test methods for raw materials.
Prepared conceptual designs and specifications, including hands-on fabrication, material and performance validation.
Plan laboratory experiments to confirm feasibility of processes and techniques used in the production of materials having special characteristics.
Prepared and maintained production reports and personnel records.
Ensured that all health and safety guidelines were followed.
Conduct Training Session of subordinates on the following topics
Management, Motivation, Inventory Control System.
cGMP/GSP
Standard Operating Procedures development
ISO 9000:2000 QMS
Work related Technical and safety training
Auditing of the system as per GMP, GSP and GLP guidelines.
Made the timely delivery of Product possible to the market.
Motivate and supervised the individuals through personal involvement to achieve the forecasted amount.
Assigned appropriate manufacturing supervisor, and operator duties.
Managed the staff of 80 individuals of, different gender, age & cultural group, as well as different economical and educational background.
Maintained necessary level of communications among staff.
Ensured that all health and safety guidelines were followed.
Assisted machine operators with finished pieces.
Successfully managed production activities so all orders were shipped on time
Met aggressive production and safety goals while minimizing equipment downtime.
Created and updated department work instructions and reports on a regular basis.
Recommended and executed quality improvements for production and product quality.
Drove daily production activities with effective communication and leadership.
Managed documentation of and training on production procedures and work instructions.
Investigated and implement ideas for quality improvement, increased productivity and cost reduction.
Immediately addressed all expired product dispositions.
Maintained and communicated daily productivity and shipment reports for all departments.
Verified that all process control parameters were being documented and followed at all times
Directly supervised the working of Forman, operators and helpers of both gender.
Conduct training session of foreman, operators and helpers regarding their work and safety precaution.
Personally involved in the Identification, Manufacturing, Packaging and delivery of Pharmaceuticals products.
Performed all in process checks in the manufacturing and packaging of Pharmaceuticals products.
Increased the efficiency of junior staff by providing good working environment and Resolved all their differences to achieve the organization goal in the shortest Possible time.
The Course work is finished Research is under process.
• Post Graduation • Doctor Of Pharmacy ( Pharm.D) • 2009-2010 ( One Year Condensed Course to upgrade the B.Pharmacy Qualification to Pharm.D) • Department of Pharmacy, University of Peshawar
• MBA • 1998 to 2000 • Institute of Management Studies, University of Peshawar
• Bachelor of Pharmacy (B.Pharm) • 1990 to 1995 • Department of Pharmacy, University of Peshawar
