Manager Engineer

CURRICULUM VITAE (CV)

Mr.Krushna Ch. Pradhan(B.Pharma,MBA )

email~ ************@*****.***

************@**********.***

Skype ID- Krushna.pradhan3

Mobile no: +91-951*******,917-***-****

Nallasopara, west, Mumbai.

CORE COMPETENCIES

Result oriented professional with of qualitative experience in pharmaceutical company across Production, Operation, International audit, Quality management system & Technology transfer.

I can contribute significantly by leveraging on my academic skills and a good level of interest in achieving the goal with my work experience.

PROFESSIONAL SYNOPSIS (B.Pharma with MBA in pharmaceutical Management)

B.Pharma with More than 13.0 years’ experience in Pharma Manufacturing in Production & Technology Transfer Department in Pharmaceutical Solid Oral [Tablet +Capsule (Powder, Pellets, ORS, ) SEMI SOLID ( Ointment,cream,gel ),Liquid, syrup,Beta lactam and Cephalosporin Dosage Form in Formulation Industry.

AUDIT FACED: As active team member in preparation.

GMP Audits, WHO – MHRA, USFDA, TGA-Australia, Russian GMP, FDA Ghana, Africa, as well as regular local FDA and ministry audit etc.

Knowledge of computers: MS-office (Word, Excel & Power point), Pharma Suite Operation and SAP, ERP.

CAREER HIGHLIGHTS

QLIFE PHARMA .DOHA, QATAR.

Manager production – june.2016 to till date

(This facility approved by the WHO, cGMP,GCC Pharma guideline)

Reporting to General Manager & CEO.

Job Profile:-

I am directly reporting to Managing Director &120 persons reporting to me.

Overall whole production planning in Tablet,Capsule,cream,Gel, General disinfectant, Semi solid and Liquid oral dosage dept. (both manufacturing &packing)

Supervision & technology transfer scale-up the production batch.

Monthly, weekly Production & packing Planning/scheduling in Solid Oral Dosage forms like Tablet, capsule, Antiseptic solution, Hand gel and disinfectant, liquid, primary, secondary packing area, Semi solid dosage form, and liquid oral dosage form.

Utilization of man, material and machinery for quality linked productivity.

To supervise and ensure compliance the various operations likes Granulation, compression, coating, capsulation, liquid, ointment etc.

To investigate the process deviation and review deviation report &CAPA.

Document preparation - SMF, BMR, BPR, VMP, SOPs, Regd. Dossier, process validation &troubleshooting of finished products.

Evacuation and investigation of all market complaints & necessary corrective and preventive actions.

To prepare monthly stock statement of RM and PM, yield statement and process loss.

Handling of Deviations, Change Controls, and CAPA as per the system.

Co-ordination with Engineer dept., R&D Plant, QA, QC, Warehouse dept. and regulatory affairs dept.

Handling of different Troubleshooting relates to the department on machine.

Training assignment to shop flower & executive, officer &pharmacist.

Set up a New OSD, OLD manufacturing facility & Validation, qualification & installation of new machinery &projects.

Supervise; Guide the team from Remaining civil, Production & Utility Installation and Qualification.

Local Manpower recruitment and the training.

Preparation/Review of all kind of GMP documents and SOP.

SOPHAL Spa, ORAN, Algeria, North Africa.

Worked as Manager- Production & Formulation.

June 2014 to May.2016

(This facility approved by the WHO, cGMP,European Directorate for the Quality of Medicines & HealthCare (EDQM) & EU Pharma guideline)

Reporting to CEO (Managing director)

Managing whole responsibilities of manufacturing as a plant-in-charge.

To plan, organize and co-ordinate all activities related to manufacturing of Tablets, Capsules and dry syrup, beta lactam, cephalosporin dept. & technology transfer development.

Utilization of man, material and machinery for quality linked productivity.

Responsible for cGMP compliance and Validations including execution review of SMF, VMP, - Protocols, Cleaning Validation, BMR/BPR’s, SOP’s etc.

Ensuring cGMP compliance /audits and Validations activities

Responsible for monthly production scheduling in coordination with SCM as well as raw - material dispensing planning according to priority & availability of RMs & PMs.

Coordination with Linked Departments like QA, QC, WH, Tech Services, Engineering, Projects, ETP & HR.

Preparation/Review of all kind of GMP documents.

Man power planning /Training Programmes /Achieving the targets / Verification of calibration of all equipment’s

Pharmalliance, North Africa, Algeria.

Production -Manager

Jul. 2012 to june.2014.

This facility approved by the WHO, cGMP and European regulary guidelines.

Reporting to Plant Manager & CEO.

Overall whole production planning, supervision & technology transfer&scale-up.

Production Planning/scheduling in Solid Oral Dosage forms like Tablet, Capsules, Semi solid dosage form and Liquid oral dosage form and package Area.

Validation, qualification & installation of new machinery &projects

Tablet, Capsules, suspension and Liquid Oral Syrup - manufacturing & technology transfer Development

Document preparation - SMF, BMR, BPR, VMP, SOPs, Regd. Dossier, process validation &troubleshooting of finished products.

Evauation and investigation of all market complaints & necessary corrective and preventive actions.

To investigate the process deviation and review deviation reports &CAPA.

Handling of different Troubleshooting relates to the department on machine.

Training assignment to shop flower & executive, officer &pharmacist.

Co-ordination with Engineer dept, R&D Plant, QA, QC,Warehouse dept. and regulatory affairs dept.

Wockhardt Ltd, Daman.india.

Shift in charge (Sr.officer)

Jan. 2011 to jul.2012.

This facility approved by the MHRA, WHO and MCA (UK).

Reporting to production Manager.

To supervise and ensure compliance the various operation likes Granulation, compression, coating and capsulation.

Review of all SOPs and prepared the new QA policy and implementation.

Utilization of man, material and machinery for quality linked productivity.

Qualification of machinery and others utility requirements.

Responsible for setting up WHO-GMP compliant solid oral dosage plants.

Daily allocation of manpower as per production plan.

Work Allocation to subordinates and collect feedback of the same.

Handling of regulatory and internal audits.

To assist in process validation in coordination with QA dept.

SAP entry, stage wise reconciliation and yield as per BMR SUBMITTED TO QA.

Interaction with engineer dept. For daily breakdown and utility requirement.

Preparation of production plan with consultant with production manager and execution of planning activity.

Sprukfield uk, sarl.Lome, Africa.

Production Executive

(January 2009 to dec.2010)

(in tablet,capsule and beta lactam dept. this facility approved by WHO-ministry of Togo, Africa)

Reporting to production Manager.

Responsibilities for entry production activity right from production planning to dispatch of finished goods. Handled the shop floor activity like, granulation, compression, coating & packing dept.

Work allocation, implement of CGMP and Training will be giving to juniors and shop floor personnel periodically.

Handling the Regulatory and CGMP Documents.

Preparation of monthly production plan to all departments. Preparation of all documents like MFR, BMR, BPR, SOP and Qualification of machine.

Review of Standard Operating Procedures (SOP’S) and handling of market complaint.

Handling of 07 officers and 25 machine engineer.

To assist in process validation in coordination with QA dept.

Co-ordination with engineer dept, R&D, Plant and regulatory affairs dept

Cipla ltd,GOA,(UNIT-III)

Management Staff(section head)

(Jan.2006 to Dec.2008)

This is represented by 21 manufacturing plants. This plant got the WHO, USFDA (USA), MHRA (U.K.), WHO-GMP, BRAJIL (ANVISA), TGA, MCC(SOUTH AFRICA), Ethiopia Health Authority, & MCA(U.K) approval.

Reporting to Head production.

Complete supervision in tablet mfg. department. Granulation, compression & Topical dept. Ointment, cream gel etc.

On job training to workman on handle the equipment and day to day production process.

Maintaining online the log book of department.

Batch mfg. record preparation and updated.

Responsibility of batch document and other record maintained.

Maintain the shift register and monitoring the same area.

Assist the responsibilities of daily scheduling projects.

Production planning and control.

Preparation of daily report and yield statement batch wise.

To make monthly plan, coordinate with production planning &export dept.

SOP preparation and rectified the same and implementation

Medibios lab LTD. Tarapur, Biosar, Mumbai.

Asst.Production Chemist

( jan.2004 to dec.2005)

This facility has already approved by WHO, cGMP.

Reporting to asst.manager.

Supervise the tablet manufacturing dept.

Preparation of daily report and submitted to assist manager.

Maintaining the daily equipment logs and other record.

Calibration and verification weigh balance.

On line entry in Batch mfg. Record and stage wise yield calculation.

Pharmaceutical Machinery Handled:

SEJONG45stn,FETTE,CADPRESS,IMA,Glatt AND GAYLARD,RMG,FBD,OGB,DCB,AUTOCOATER 51’’ AND 67’’,IMA CAPSULE FILLING MACHINE.

BLISTER AND STRIP PACK MACHINE, Liquid mfg. tank & filling machine (Both semi solid syrup line)

Sticker Labelling machine, Cartonater Machine PAMPACK & CHINA.

ACADEMIC QUALIFICATION

Exam passed Board/ University Year Percentage

B. Pharma Berhampur University oct.2003 62.0%

MBA in pharmaceutical Management National institute of business management May.2017 78.0 %

(Chennai, India)

Inter (10+2) CBSE Board, Orissa 1999 52.0 %

10 th std. Council of Higher Secondary Education, Orissa 1997 65.0 %

COMPUTER TECHNIQUE

Computer Packages : Microsoft Office 2000 & 200*-****-**** 2013.

Operating Environment : Windows 7, 8 & 10.

Electronic Communication : Email, Internet. SAP.

Father’s Name : Shri Ladu Kishore Pradhan

Date of Birth : 10.05.1980

Sex : Male

Marital Status : married (wife & two daughter’s)

Religion : Hindu

Nationality : Indian

Languages Known : English, Hindi & Oriya and French.

Passport no. : G6374189

Skills:

Ability to work in challenging situation.

Flexibility in working style.

Time management Skills.

Ability to work with people.

Target Achievement.

Bravery.

Strengths:

Learning Attitude.

Positive Attitude.

Responsibility.

Hard working.

Punctuality.

Faithfulness.

I hereby declare that the above furnished information is true to my knowledge.

Date:

Place: (KRUSHNA CHANDRA PRADHAN)

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