• Gender: Male
• Age: 39
• Designation: Department Head
• Highest Education Level: Diploma
• Current Gross Salary: INR  240000 /Annum
• Expected Gross Salary: INR  340000 /Annum
• Preferred Country: India
• Work Experience: 13.7 Year(s)

Education

B.Sc appearing in MANAV BHARTI UNIVERSITY (OPEN)
Three- Month full time training course on Packaging from Indian Institute of Packaging, Mumbai accredited by the Asian Packaging Federation.
Diploma in Packaging Technology from B.I.T College under W.B.S.C.T.E, Kolkata (West Bengal). 2009-2011
Grade: 1st Class (Distinction)
Diploma in Hardware and Networking from Brainware under Jadavpur University, Kolkata (W.B).2008-2009
Grade: Excellent
H. Sc. Science from JDPHS School under W.B.C.H.S.E, Mecheda (W.B).2005-2007
Grade: 2ND Class
Secondary from G.G.P.N.B.B, under W.B.B.S.E, Mecheda (W.B). 2002
Grade: 1ST Class

Skill Sets

A dynamic professional with more than 2 years + of rich experience in Quality Analysis / Quality Control / Quality Assurance/ TQM and System implementation in manufacturing set up.
Proficient in Quality Control activities along with implementation of various techniques for improving the operations along with cost effectiveness.
Keen interest in Quality Analysis / Control / Assurance / Total Quality Management and System Implementation. Compiling reports and database, Data Analysis for quality product.
An effective communicator with excellent managerial skills and strong analytical, problem solving & organizational abilities.

Work Experience

Q.C Head – Quality Control.
Since Feb. 2013
Company Profile: Manufacturing of Printed Carton to fulfill the requirements of Pharmaceuticals and Health Science
Accountabilities & Responsibilities:
Overall accountability of QC functions.

Assistant (Quality Control).
April 2012 - Feb. 2013
Company Profile: Manufacturing of Printed Carton to fulfill the requirements of Hindustan Unilever Ltd., Godrej Sara Lee Ltd., Glaxo Smithkline Health Care Ltd. S. C. Johnson Products Ltd., Emami Ltd., Procter & gamble, Torrent pharma, Intas. Cipla Ltd. etc.
Accountabilities & Responsibilities:
Overall accountability of QA functions.
Overall responsibility of GMP & system implementation

Q.C Inspector – Quality Control
June 2011 - March 2011
Nextgen Printers Pvt. Ltd
Accountabilities & Achievement:
Prepared an effective plan for printing Quality Analysis and implemented.
Improvement in printed Product by reducing unwanted foreign matters by adjusting the Process Feed Ratio.
Implementation of Non-Conforming Product Control System.
Validation of Process and Implementation of in-house Validation of Measuring & Monitoring Devices (Weighing Scale) for better monitoring.
SAP entry for all printing machine documentation.
Good knowledge about shade judgment and text matter.

Accountabilities & Accomplishments:
All types of raw material testing like as paperboard, adhesive, varnish and ink
Reduction in on-line rejection of Raw and Packaging Materials by implementing the effective sampling plan.
Standardization and implementation of the method of instant analysis of all type documentation
Implementation of Non-Conforming Product Control System.
Good knowledge about in process inspection and final inspection.

Accountabilities & Responsibilities:
Quality Control & Inspection:
Overall accountability of testing of in-coming raw materials, packaging materials for acceptance of good quality input materials for the process.
Overall accountability of testing & inspection of in-process materials and finished product for ensuring the consistency in product quality as per the customer requirement.
Calibration & Validation:
Responsible for ensuring the calibration activity of all identified equipments for calibration by liasoning with the competent authority for out-house calibration to ensure the consistency in operation as required by customer.
Responsible for in-house validation of all identified equipments and to ensure the smooth operation.
Responsible for Validation of Process to ensure the consistency in Product Quality.
Process Management & System :
Responsible for smooth functioning of QA activities by executing the deployment of resources as per shift to achieve the departmental as well as organizational objectives.
Responsible for implementation of quality standards and stringent quality control systems to enhance quality of products and reduce rejection level through continuous adherence of ISO systems to observe better compliance in line with changing market/ customer requirement.
Responsible for executing and monitoring the systems and processes that implemented for enhancement of QA activities.
Analysis & Improvement:
Responsible for data collection and analysis for setting new specification of In-process materials & finished product as per the changing demand of customer.
Responsible for data collection and analysis of vendor’s performance of supply of all raw and packaging materials for enhancement of quality of input materials for smooth operation as well as customer requirement.
Responsible for raising CAPA wherever required and to ensure that the raised CAPA has been implemented and closely monitored.
Responsible for conducting root-cause analysis of customer complaint (if any) and to find out the critical control point of the process for further monitoring.

Resource Management:
Responsible for planning for resources (Both Man-power & Infrastructure)
Responsible for deployment of Man-power as per daily production schedule intimated by Production department.
Responsible for preparation of Skill Mapping, Competency Matrix, Skill Gap and Training Need Identification for sub-ordinates and to ensure that the identified sub-ordinates are trained.

Records & Communication:
Responsible for maintaining the Documents and Records as per QMS requirements.
Responsible for communicating the concerned authorities in case of any non-conformity in product and to ensure no such material reaches to the user.

B] Achievements:
Laboratory Set-up:
Set up of QA Laboratory for all QA activities.
Preparation of Standard Operating Procedure of all the equipments.
Preparation of Standard Operating Procedure for all the activities of QA.

Documentation :
Preparation of Process Map & Quality System Procedure as per QMS requirements.
Preparation of Standard Operating Procedure of every operation and process.
Designing & preparation of Formats as per the QMS as well as Management requirement.

Records :
Designing and preparation of proper recording system of data of every activity as per Management requirement.
Initiated data analysis of every activity and preparation of Analysis report.

Training & Development :
Evaluation of training needs identification for subordinates and conducting Training.
Periodical training on System and GMP.

Implementation & Improvement :
Iniatiated for proper implementation of GMP and system developed in concern areas.
Initiated the follow-up system for close monitoring and improvement of system.
Initiated the implementation of Quality Circle & 5S within the organization.

Internal Audit & Follow Up:
Initiated in conducting Internal Audit and review meeting to ensure the adherence of system.

Future Goals

In quest of challenging assignments in the field of Total Quality management
/ Control / Assurance involving Total Quality & Process Enhancements / Data Analysis & Improvement / Vendor Assessments with a growth oriented Organization which offers an excellent environment for learning and growth by implementing the analytical skill enabling me to achieve to the fullest thereby helping me to contribute the maximum towards the organizational productivity as well as individual development.