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SARAVANAKUMAR.D
4th
Industrial City, Jeddah,
Kingdom of Saudi Arabia
Skype: SARAVANAKUMAR
DEVAN
Nationality: Indian.
Mob.: 00966563656919
devjisaran1984@yahoo.in
devjisaran1984@gmail.com
CAREER OBJECTIVE:
An Enthusiastic, hardworking professional seeking to obtain a challenging
position providing professional career growth in the pharmaceutical / biotech
industry
EXECUTIVE SUMMARY:
 Bachelor of Pharmacy with 11 year Experience in Pharma filed.
 Presently working as an Head of Mfg. for (3 unit-APM).
 Extensive experience in planning, arrangement & production with the
knowledge of managing the day operations in a committed dedicated
team player, Fast learning and result oriented ability
 Excellent Inter-Personal Relationship Management and Problem
Solving Skills
 Honors:
 Received award for launching a new product and Admin Man power
Reduced,
 Achieved 170% target of MOH-Tender product/admin participated star
club awards function in HOLIDAY INN, Half-moon bay Saudi Arabia.
2014 managed the Pharma plant unit-1 PM, {3 times reward’s in KSA & 2
times in India}
 Achieved cGMP, ISO, FDA got approval as an appreciated by
Management,
 TPM & new Project - ABBOTT, MERCK (MSD), TAKEDA, Pharma-g UK,
MOH(Saudi, oman, uae), Servier
 Received EXCELLENCE Performer Award for achieved MOH Tender/
audit unbelievable out-put and appreciated by GM Batterjee -2016,
WORK EXPERIENCE:-
Present Organization:
 Head of Mfg. for (3 unit-APM) at Batterjee Pharmaceuticals (BHC)., KSA
Duration: From March 2016 to till
Previous Experience:
 APM as an world rep., Kingdom of Saudi Arabia, UAE, Bahrain, India From
March 2015 to march.2016
 Assistant Manager Production,{plan/QA} in Montajat Pharmaceuticals Co
Ltd., Kingdom of Saudi Arabia. From December 2010 to march.2015
 Worked as an Assit.Plan/plant Manager rolls in montajat Jan to Oct. 2014
 Worked as an Executive Production/QA in Bal Pharma Ltd,{Micro Lab
Group} Bangalore, Karnataka From March 2007 to November 2010.
 Worked as a Training in-charge in Medibest Pharma, Hosur, Tamil nadu
From September 2005 to March 2007.
 In-plant Training at TTK Healthcare, Chennai. 2004.
CURRICULAM VITTAE
Personnel Details:
Passport No: H4944484
Driving License:India&GCC
Father Name:P.Devan-HM
Gender: Male
Date of Birth: 30.07.1984
Nationality: Indian
Religion: Hindu
Permanent Address:
Muthagaundanur (vill)
Puthagaram (post)
Pudupet(via)
Tirupathur{tk}
Vellore{dt}
Tamil Nadu{state}635651
Cell: +919994619299
Home: +919585726103,
Language Known:
English,
Hindi,
Arabic,
Kannada &
Tamil
Hobbies:
Reading Books,
Traveling,
Listening Songs
irpattur(T
K)Vellore
(DT)
milnadu
(State)
Pin:
635651
: English, Hindi, Arabic,
Kannada Tamil
Languages Known :
English, Hindi, Tamil,
Kanada, Malayalam,
WORKING ROLE:
Production / QA/ Planning assist. /Production coordinator/WH
 TPM & New project and production new line modification.
 Over all experience in (Solid, liquid, external)
Liquid,
OSD- powder
Tablet
Capsule
External – Ointments etc.
Sterile injection secondary and RM…
New product dev. Tablet, liquid, external, powder, OSD
Working exposure with various compositions (Granulation,
Compression, Coating, Blending, Capsule filling, all Packing line, Mfg.,
dispensing and all doc. Record submission)
 Arranging a PP, Packing and Raw Material for Production.
 Handling of IPQC instrument like Ph. Meter, Conductivity Meter, BD,
friability, dis,HT,VC,INS.,DT, particle count, Or, and all production/IPQC
instruments etc….
 Raw Material dispensing {LAF/CIP/Auto}and PM
Production {Pharma & bio-pharmaceuticals/Bulk}, Packing, Store RM,
Planning
 Knowledge about formulation/Machine Installation-Operation/QA
knowledge and Strong problem solving knowledge of all stages of
Mfg./packing,
 Exposure in working towards facing the cGMP, FDA-Saudi audits.
 Preparation / review of SOP for manufacturing / equipment’s.
 Effective Manpower utilization along with production plan. Cost saving
 Knowledge about costing and department budgeting.
 Dedicated to providing quality and fast accurate medication serve.
 Redesigned workflow and requirement as well as to cover the new plan.
 WIP Statement Clearance & Planning, Idle and product problem solving.
 Review of existing facility and recommending the management for
improvement and upgrading of facilities, equipment’s.
 Coordination with inter and intra departmental functions, tracking and
monitoring production processes to reduce raw material/packing
material wastages and to improve yields and efficiencies.
 Scheduling the production and documentation work. Guide and train
the subordinate,
 Work exposure in safety measures.
 Team management to achieve the targets in less time with good quality.
 Knowledge about MFR, BMR, BPR, APQR, IPQA & COPP, Managing IPQA
work and QA documentation issue & review Production/QC doc. CAPA,
CC, QPR etc.
 Line Clearance and In-process checks in Manufacturing and Packing
Area.
 Review of Batch Manufacturing Record after each stage and final
packing.
 Handling and documenting Change Control and Deviation.
 COA, SOP {OP&CL},CALIBRATION
 Calibration and all usage doc. Format maintained
 Line clearance, check in and format finalize
 RM/PM/BULK/FP/FD-S/STABILITY data sheet verifying and Log book maintain.
 Co-ordinate:
ISO-doc., Plant site QA, MSF Handling
Method Validation
Calibration
Protocol {product/method/equipment/system}
Qualification
APR/QPR/STP- Standard test Procedure,
Product recall and compliant analyze,
ISO- AND SITE Master file handling,
Analytical work record approval RM/PM/BULK/FP
Preventive maintenance and Work record creation.
 Material receiving and preparing a QC/QA doc.
 Conducting classroom training related to cGMP and imparting knowledge for
operators. Impart training to all new emp. regarding SOP/cGMP.
 Updates and reviews Process records. Production Work Orders closing {4S}
 Identification/Labeling of all areas & equipment’s.
 Sampling all formulation stage and In-process checks-Process Validation Samples.
 Involved in Equipment Validation (Preparation of Qualification Documents of
Equipment’s like URS, DQ, IQ, OQ and PQ protocols & reports).
 Billing document verify and close a 4s’, WIBI, ERP, SAP, CIPS Software.
 Monitoring and supervising shop floor activities (IPQA).
 Actively involved in calibrations, validations.
 IPQA activities in dispensing and warehouse.
 Maintain the online documentation.
 Receiving, checking and approval of stereos.
 BMR (Batch manufacturing record), BPR (Batch packaging record) receiving and
review.
 In-process and Finished Product Sampling.
 Sampling of drug products from regular batches and validation batches.
 To monitor Bulk Packing Activities.
Human Resources/Admin:
Managing Company HR works, Maintain various employee records and expiry
Passport, Labor Card, ID, Bank salary cards- manual, warehouse, retails etc.,
Annual leave records booking air tickets, Managing daily attendance and Forms,
Over time forms, Absent forms, Leave forms, Filling Work as required, Common
Corers, Staff Details, Drafting Letters, Memo & Warning Letters, interview
schedule.
Trail exp. In Tablet, Capsule, Oral liquid, powder, external pre. Solution.
Customer/Country Audits faced:
Zambia, Sudan, Myanmar, Namibia, Nigeria, Chili, Malawi, Iraq, Ethiopia, Kenya,
Morocco, Brazil, Yemen, DI&DC, SFDA, TN, KN, AP & ASSAM GOVT. Training of MHRA,
Micro lab, Medo-Pharma etc.
References:
Name Mr.K.Vinayagam Contact No. 00966560378599
Professional Relationship Montajat pharma E-mail Vinmio_2003@yahoo.co.in
Job Title QCM Address Kingdom of Saudi Arabia
Mr.Ameed Ansari CEO info@montajat.biz
Name Dr.K.P.Magesh Contact No. 0091-9448382553
Professional Relationship Bal pharma – AGM E-mail Kpm6@rediffmail.com
Job Title Assistantant GM (quality) Address Bangalore
Training Programmes /Seminars attended:
NSS – National Social Service participated,
BRC- Block Resource Class participated and meeting arr.
IPC – President Dr.Suresh Participate attend.
Carrier Point job Training Participated.
* Seminar attended in India {Safety}, MHRA
* Training programme, includes Basic and practical training with respect to PLC and
Machine installation, Zufang corporation China team in Saudi Arabia.
Achievements:
* undergone the cGMP & ISO 9001:2000 audit in the year 2010 and got approval
in my previous companies.
* undergone the Saudi FDA audit in 2013 in Montajat pharmaceuticals company,
Dammam, KSA, and got approval in 2014.
AUDIT SPACED:
GMP
ISO”
MHRA
FDA {Saudi}
ABBOTT, MERCK (MSD), TAKEDA, Servier, Pharma-g UK, MOH(Saudi, oman, uae)
Customer audit Domestic and overseas,
EDUCATIONAL QUALIFICATION:
 Bachelor of Pharmacy in Dr. M.G.R. Medical University, TamilNadu, India.
 Computer and office Management,
 (MBA) {Annamalai University}
 BA {Annamalai University}
 D.Ted {KN Government Board Exam}
DECLARATION:
I do hereby declare that the above mentioned information are true and correct to the
best of my knowledge and belief.
Place: Yours faithfully
Date: (SARAVANAKUMAR.D)
EDUCATIONAL QUALIFICATION:
 Bachelor of Pharmacy in Dr. M.G.R. Medical University, TamilNadu, India.
 Computer and office Management,
 (MBA) {Annamalai University}
 BA {Annamalai University}
 D.Ted {KN Government Board Exam}
DECLARATION:
I do hereby declare that the above mentioned information are true and correct to the
best of my knowledge and belief.
Place: Yours faithfully
Date: (SARAVANAKUMAR.D)

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Dr.SaravanaKumar - Production- Plan and QA CV (3)

  • 1. SARAVANAKUMAR.D 4th Industrial City, Jeddah, Kingdom of Saudi Arabia Skype: SARAVANAKUMAR DEVAN Nationality: Indian. Mob.: 00966563656919 devjisaran1984@yahoo.in devjisaran1984@gmail.com CAREER OBJECTIVE: An Enthusiastic, hardworking professional seeking to obtain a challenging position providing professional career growth in the pharmaceutical / biotech industry EXECUTIVE SUMMARY:  Bachelor of Pharmacy with 11 year Experience in Pharma filed.  Presently working as an Head of Mfg. for (3 unit-APM).  Extensive experience in planning, arrangement & production with the knowledge of managing the day operations in a committed dedicated team player, Fast learning and result oriented ability  Excellent Inter-Personal Relationship Management and Problem Solving Skills  Honors:  Received award for launching a new product and Admin Man power Reduced,  Achieved 170% target of MOH-Tender product/admin participated star club awards function in HOLIDAY INN, Half-moon bay Saudi Arabia. 2014 managed the Pharma plant unit-1 PM, {3 times reward’s in KSA & 2 times in India}  Achieved cGMP, ISO, FDA got approval as an appreciated by Management,  TPM & new Project - ABBOTT, MERCK (MSD), TAKEDA, Pharma-g UK, MOH(Saudi, oman, uae), Servier  Received EXCELLENCE Performer Award for achieved MOH Tender/ audit unbelievable out-put and appreciated by GM Batterjee -2016, WORK EXPERIENCE:- Present Organization:  Head of Mfg. for (3 unit-APM) at Batterjee Pharmaceuticals (BHC)., KSA Duration: From March 2016 to till Previous Experience:  APM as an world rep., Kingdom of Saudi Arabia, UAE, Bahrain, India From March 2015 to march.2016  Assistant Manager Production,{plan/QA} in Montajat Pharmaceuticals Co Ltd., Kingdom of Saudi Arabia. From December 2010 to march.2015  Worked as an Assit.Plan/plant Manager rolls in montajat Jan to Oct. 2014  Worked as an Executive Production/QA in Bal Pharma Ltd,{Micro Lab Group} Bangalore, Karnataka From March 2007 to November 2010.  Worked as a Training in-charge in Medibest Pharma, Hosur, Tamil nadu From September 2005 to March 2007.  In-plant Training at TTK Healthcare, Chennai. 2004. CURRICULAM VITTAE
  • 2. Personnel Details: Passport No: H4944484 Driving License:India&GCC Father Name:P.Devan-HM Gender: Male Date of Birth: 30.07.1984 Nationality: Indian Religion: Hindu Permanent Address: Muthagaundanur (vill) Puthagaram (post) Pudupet(via) Tirupathur{tk} Vellore{dt} Tamil Nadu{state}635651 Cell: +919994619299 Home: +919585726103, Language Known: English, Hindi, Arabic, Kannada & Tamil Hobbies: Reading Books, Traveling, Listening Songs irpattur(T K)Vellore (DT) milnadu (State) Pin: 635651 : English, Hindi, Arabic, Kannada Tamil Languages Known : English, Hindi, Tamil, Kanada, Malayalam, WORKING ROLE: Production / QA/ Planning assist. /Production coordinator/WH  TPM & New project and production new line modification.  Over all experience in (Solid, liquid, external) Liquid, OSD- powder Tablet Capsule External – Ointments etc. Sterile injection secondary and RM… New product dev. Tablet, liquid, external, powder, OSD Working exposure with various compositions (Granulation, Compression, Coating, Blending, Capsule filling, all Packing line, Mfg., dispensing and all doc. Record submission)  Arranging a PP, Packing and Raw Material for Production.  Handling of IPQC instrument like Ph. Meter, Conductivity Meter, BD, friability, dis,HT,VC,INS.,DT, particle count, Or, and all production/IPQC instruments etc….  Raw Material dispensing {LAF/CIP/Auto}and PM Production {Pharma & bio-pharmaceuticals/Bulk}, Packing, Store RM, Planning  Knowledge about formulation/Machine Installation-Operation/QA knowledge and Strong problem solving knowledge of all stages of Mfg./packing,  Exposure in working towards facing the cGMP, FDA-Saudi audits.  Preparation / review of SOP for manufacturing / equipment’s.  Effective Manpower utilization along with production plan. Cost saving  Knowledge about costing and department budgeting.  Dedicated to providing quality and fast accurate medication serve.  Redesigned workflow and requirement as well as to cover the new plan.  WIP Statement Clearance & Planning, Idle and product problem solving.  Review of existing facility and recommending the management for improvement and upgrading of facilities, equipment’s.  Coordination with inter and intra departmental functions, tracking and monitoring production processes to reduce raw material/packing material wastages and to improve yields and efficiencies.  Scheduling the production and documentation work. Guide and train the subordinate,  Work exposure in safety measures.  Team management to achieve the targets in less time with good quality.  Knowledge about MFR, BMR, BPR, APQR, IPQA & COPP, Managing IPQA work and QA documentation issue & review Production/QC doc. CAPA, CC, QPR etc.  Line Clearance and In-process checks in Manufacturing and Packing Area.  Review of Batch Manufacturing Record after each stage and final packing.  Handling and documenting Change Control and Deviation.
  • 3.  COA, SOP {OP&CL},CALIBRATION  Calibration and all usage doc. Format maintained  Line clearance, check in and format finalize  RM/PM/BULK/FP/FD-S/STABILITY data sheet verifying and Log book maintain.  Co-ordinate: ISO-doc., Plant site QA, MSF Handling Method Validation Calibration Protocol {product/method/equipment/system} Qualification APR/QPR/STP- Standard test Procedure, Product recall and compliant analyze, ISO- AND SITE Master file handling, Analytical work record approval RM/PM/BULK/FP Preventive maintenance and Work record creation.  Material receiving and preparing a QC/QA doc.  Conducting classroom training related to cGMP and imparting knowledge for operators. Impart training to all new emp. regarding SOP/cGMP.  Updates and reviews Process records. Production Work Orders closing {4S}  Identification/Labeling of all areas & equipment’s.  Sampling all formulation stage and In-process checks-Process Validation Samples.  Involved in Equipment Validation (Preparation of Qualification Documents of Equipment’s like URS, DQ, IQ, OQ and PQ protocols & reports).  Billing document verify and close a 4s’, WIBI, ERP, SAP, CIPS Software.  Monitoring and supervising shop floor activities (IPQA).  Actively involved in calibrations, validations.  IPQA activities in dispensing and warehouse.  Maintain the online documentation.  Receiving, checking and approval of stereos.  BMR (Batch manufacturing record), BPR (Batch packaging record) receiving and review.  In-process and Finished Product Sampling.  Sampling of drug products from regular batches and validation batches.  To monitor Bulk Packing Activities. Human Resources/Admin: Managing Company HR works, Maintain various employee records and expiry Passport, Labor Card, ID, Bank salary cards- manual, warehouse, retails etc., Annual leave records booking air tickets, Managing daily attendance and Forms, Over time forms, Absent forms, Leave forms, Filling Work as required, Common Corers, Staff Details, Drafting Letters, Memo & Warning Letters, interview schedule. Trail exp. In Tablet, Capsule, Oral liquid, powder, external pre. Solution. Customer/Country Audits faced: Zambia, Sudan, Myanmar, Namibia, Nigeria, Chili, Malawi, Iraq, Ethiopia, Kenya, Morocco, Brazil, Yemen, DI&DC, SFDA, TN, KN, AP & ASSAM GOVT. Training of MHRA, Micro lab, Medo-Pharma etc.
  • 4. References: Name Mr.K.Vinayagam Contact No. 00966560378599 Professional Relationship Montajat pharma E-mail Vinmio_2003@yahoo.co.in Job Title QCM Address Kingdom of Saudi Arabia Mr.Ameed Ansari CEO info@montajat.biz Name Dr.K.P.Magesh Contact No. 0091-9448382553 Professional Relationship Bal pharma – AGM E-mail Kpm6@rediffmail.com Job Title Assistantant GM (quality) Address Bangalore Training Programmes /Seminars attended: NSS – National Social Service participated, BRC- Block Resource Class participated and meeting arr. IPC – President Dr.Suresh Participate attend. Carrier Point job Training Participated. * Seminar attended in India {Safety}, MHRA * Training programme, includes Basic and practical training with respect to PLC and Machine installation, Zufang corporation China team in Saudi Arabia. Achievements: * undergone the cGMP & ISO 9001:2000 audit in the year 2010 and got approval in my previous companies. * undergone the Saudi FDA audit in 2013 in Montajat pharmaceuticals company, Dammam, KSA, and got approval in 2014. AUDIT SPACED: GMP ISO” MHRA FDA {Saudi} ABBOTT, MERCK (MSD), TAKEDA, Servier, Pharma-g UK, MOH(Saudi, oman, uae) Customer audit Domestic and overseas,
  • 5. EDUCATIONAL QUALIFICATION:  Bachelor of Pharmacy in Dr. M.G.R. Medical University, TamilNadu, India.  Computer and office Management,  (MBA) {Annamalai University}  BA {Annamalai University}  D.Ted {KN Government Board Exam} DECLARATION: I do hereby declare that the above mentioned information are true and correct to the best of my knowledge and belief. Place: Yours faithfully Date: (SARAVANAKUMAR.D)
  • 6. EDUCATIONAL QUALIFICATION:  Bachelor of Pharmacy in Dr. M.G.R. Medical University, TamilNadu, India.  Computer and office Management,  (MBA) {Annamalai University}  BA {Annamalai University}  D.Ted {KN Government Board Exam} DECLARATION: I do hereby declare that the above mentioned information are true and correct to the best of my knowledge and belief. Place: Yours faithfully Date: (SARAVANAKUMAR.D)