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Pharma Production Manager Resume Sample, Experience : 15 years

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Name of the Candidate:[Private]
Name of the Post Applied:Pharma Production Manager
Job related skills / software:To Ensure quality output with optimum utilization and safety of Men, Material, Method & Machinery to achieve production targets.
Category:Medical
Sub Category:Chemist
Years of Experience:15 years
State:Andhra Pradesh
Gender:Male
Salary Expected per Month(Rs):70,000 to 80,000
Highest Qualification attained:M.Sc. / MSC : Master of Science
Major / Specialization:Chemistry
Email Id:[Private]
 
Are you looking for job now?:Yes
Can the recruiter contact you?:Yes
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Resume Format / CV Sample Template / Example / Model :

    

Resume  :
K.Manohar,
Near vinayaka temple,
Unagatla(post)
Cha gallu (Mandal)
West Godavari District, 534347. A.P

Phone  : 9000102750, 9848684000
E-mail  : manoharkudapa AT rediffmail.com

Objective  :
To secure challenging position where my knowledge can be best utilized successful consummation of any assignment and to be real asset to the organization in terms of gaining shaving and development adroitness.

Educational Qualification  :
** M.Sc (chemistry)from Kuvempu University in the Year 2006 with an average percentage of 63.8%.
** B.Sc (Chemistry)from Andhra University in the Year 2003 with an average percentage of 63.33%.
** Intermediate from SBIE, Hyderabad in the Year 2000 with an average percentage of 48.6%.
** S.S.C from BSE, Hyderabad in the Year 1998 with an average percentage of 61.5%.

Experience  :
Having 14+yeas of experience in API & Intermediates production.
Working as Dy.Manager (production) in SMILAX LABOATORIES LTD. from Sep-2014 to till date.
(An ISO 9001  :2008 & EDQM Approved company)

Worked as shift in charge (production) inDIVIS LABOATORIES LTD. from July-2003 to May- 2014
(An ISO 9001  :2008, ISO 14001:2004,OHSAS-18001:2007Certified & EDQM ,
US FDA,WHO, TGA,JAPAN,KORIEAN Approved company)

Strengths  :
** Ability to lead a group towards desired objectives
** I wish to promote your organization through self- motivated way as my level best
** I wish to submit myself t meet the expectation on me from the organization.

Job Profile&Responsbilities  :
** Good exposure of processes and Unit operations in API &Intermediates.
** Responsible for entire block operations like production planning & Execution.
** To Ensure quality output with optimum utilization and safety of Men, Material, Method & Machinery to achieve production targets.
** Execution of monthly production plan by ensuring the availability of Raw materials, Machine, Manpower etc..and also implement action plan for achieving management objectives
** Develop and monitor compliance with production plans in relation to the production unit.
** Plan and ensue maintenance of stocks of Raw material, packaging material and other consumables at plant or in store.
** Supervising production and documentation in compliance with USFDA,TGA,WHO and other regulatory agencies guidelines.
** To identify the training needs of department personnel based on training needs and evaluate effectiveness of training.
** Coordinating & supporting other functional departments likeQA, QC, Stores, R&D, Maintenance, and Process & HR in resolving the issues related to production.
** Generate and implementinnovative ideas in area of; Cost Reduction, Productivity increase, Quality improvements, Resource reduction, System improvements, Waste Minimization.
** To process through knowledge of Machinery and Trouble shooting of them.
** Operation and maintenance of clean Rooms & Sanitation.
** Preparation & ensuring the relevant SOPs, BMRs, Master Formulas are in place for smooth running of production activities.
** Handling of Deviations, Change Controls, and Incidents. Making sure that all production Deviation are reported, Evaluated and those Critical Deviations are investigated and the conclusions are recorded.
** To ensure Safety Work Permits & Evaluation of safety Procedures.
** Establish or Up-Date all documentation in relation withQuality and Safety Systems adopted by Organization.
** Guide & Motive workforce of Staff/Officers & workmen to activeproduction targets within the framework of Quality & Safety, utilizing optimum quantity of materials, with efficient use of machine, energy & manpower.
** Undertake process Troubleshooting, New Process Implementation, Modification etc.


in the plant/unit.
** To prepare, review and distribute the instructions for the production of Intermediates or APIs as per written procedures.
** Making sure that Validation Protocols and reports are reviewed and coordinate in concluding of OOS & OOT.
** Prepare & Review of Daily Production Reports, Monthly Production Planning & Monthly Production Statements (Including WIP , Physical stock and Monthly Solvent date.)
** Coordinating & supporting other functional departments like QA ,QC ,WAREHOUSE ,R&D, MAINTENANCE ,and process &HR in resolving the issues related t production.
** preparation of WIP and Physical stock statement of solvents, Raw material, Intermediates & Finished products for Quarterly and Annual stock Audits.
** To control f the EMISSIONS and look into the feasibility of reduction of Effluent and Emissions.
** Planning for solvent recovery and reusability to minimize product cost and preparation of monthly solvent Data for monthly CCs
** Initiate and investigate production relatedChange control, deviations and incidents, CAPA to be taken for same. And team member to find out Route causes and take Corrective & Preventive actions for the Non-Conformities by Internal and External Audits.
** To Ensure Blending advise as per Customer requirement and also Cross Checking f Blender & Blending material.
** Make sure that Internal Audit and External audit Findings are closed in time.
** Preparation & and review allMaster production Records.
** To maintain and ensure the updated documents ofCGMP
** prepare and review of the documentations as per Surveillance Audits & Customer requirements.
** To check and review of Daily production reports & CC Statements

About Facility  :
** This block is multi product API plant which designed to bulk production o check and review of Daily production reports & CC Statements
** This black having all kind of equipments like GLRS,SSRS, centrifuges, ANFDS dryers,multimill,blendrs,multi mill & sifters
** All activities in the plant maintain cGMP
** Total 30 staffs are working including executives and officers

Achievements  :
** Successful completion of Regulatory audits like USFDA, EDQM, KORIEN FDA, WHO, ISO
** Successful completion of validations of different kind of products(API & Intermediates)

Projects Doing  :
Pantoprazole sodium, Losartan potassium, Lansoprazole pharma, valsartan, sil –cyclised, Atorvastatin Calcium, Norfloxacin,

Personal Profile  :
Name  : KUDAPA MANOHAR.
Father’s Name  : K. Venkata Krishna Rao.
Date of Birth  : 10-04-1983
Gender  : Male.
Languages Known  : English, Telugu
Marital Status  : Married.
Contact Address  : K.Manohar
Near venayaka temple
Unagatla(post),chagallu(mandal)
West Godavari dist,A.P-534347

Declaration  :-
In view of the above, I request you to kind enough to give me an opportunity to service in your esteemed organization in the capacity mentioned above for which act of kindness I shall be a very thankful to you.

I here by declare that the above written particulars are true to the best of my knowledge and belief.

Date  :
Place  :

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