Manager Plant

Cover Letter : :

From:

Vinod Chandra Chaubey

B-29 Nandandham Society,

Near Air Force Station,

Makarpura, Baroda(Gujarat)

Pin-390010

Mob:094********, 081********

A good professional having 21 years of experience in the field of manufacturing of API and intermediates through batch process, DCS, PLC operation systems. Expertise in handling of the sophisticated equipments like Preparative HPLC, Lyophilizer,Isolators and different types of filtration systems like MF, UF, NF, R O. Experience of working in clean area of class 100000 ( ISO Class 08 ), exposure for the audit of the facility by regulatory agency USFDA, EU GMP, TGA, ANVISSA, WHO and state GMP/Safety as a team leader production.

Completed education from VBS Purvanchal University, Jaunpur and started career with Bulk drugs (API) industry. With my strong will power / dedication to do some extraordinary works, I found myself successful in each segment of my career and believe that my strong work ethic will be an asset for the company.

Now I would like to forward my resume, please find the same and get back to me as soon as possible.

With warm regards,

Vinod Chandra Chaubey

Attached - Resume.

CURRICULUM-VITAE

VINOD CHANDRA CHAUBEY

B-29 Nandandham Society

Behind Air Force Station

Makarpura, Baroda (Gujarat)

Mob. 094********,081********

E-Mail ID:-*****************@*****.***

Objective:

Looking for a challenging position as a DGM/GM operation in a growth-oriented organization, which could help me

by providing the Job opportunity to utilize my potential in reaching the organization up to the next projected level.

Career Profile:

Efficient, versatile, result-oriented, high-energy, self motivator, self starter, strive to get new challenges, Positive attitude,

hands-on professional with a successful record of accomplishments in the field of manufacturing, proven ability to lead

and motivate a team. Presently responsible for managing the operations of a fast growing Oncology/ General API

manufacturing company having the presence in regulatory market.

Major strength include strong leadership, excellent communication skills, competent, strong team player, very keen to

accept the new challenges, self starter, self disciplined and positive attitude, well aware about the documentation

of ISO9001:2008,ISO14000:2004,OHSAS 18001:2007, current good manufacturing practices and a clear vision to

accomplish the company goals. Well versed in the operation of MS Office and basic computer techniques.

Major area of expertise include DCS operation, SAP systems, clean area class 100000 ( ISO Class 8 ) and

Lyophilizer, Isolator, water purification systems, different type of filtration systems like Micro Filter, Ultra Filter,

Nano filter, Westfalia decanter, Prep HPLC, Tubular centrifuge, Bromine ISO tanker, handling of Chlorine

tonners, uses of NaH, Solvent recovery and distillation (Batch distillation, Vacuum distillation,

azeotropic distillation, fractional distillation). Unit operation like centrifuging, solvent distillation,

filtration under vacuum, drying under vacuum. Well versed in the operation of ANFD, FBD, sparkler filter,

Leaf filter, SS and Glass lined reactors. Executed safely various reactions i.e.Grignard reaction,

Bromination, Chlorination, Nitration, Cynation, Hydrolysis, Sulphonation reaction, Displacement reaction,

Esterification, Neutralization, Condensation, Reduction, oxidation, Methylation and Fidel Crafts Reaction.

Professional Experience: 21 Years

1.Currently working as a Head Production in M/s BDR Life Science PVT, Ltd, Luna ( Baroda )

(Gujarat), A fast growing CGMP, ANVISA, EUGMP approved and KFDA audited facility engaged in the

production of Oncology/ General API . Oncology production ranges from 50 Gm to 40 kg batch size.

CA: May. 2016 - Present.

Head Production

Product: Zefitinib, Erlotinib hydrochloride, Capecitabine, Bortezomib, Bendamistine Hydrochloride, Fosfomycin Disodium, Desvelafexine Succinate, Abiraterone acetate, Pemetrexed Disodium Heptahydrate, Tegafur, Imatinib Mesylate etc.

.

Job Profile:

Leading and managing of two manufacturing plants of General API and of Oncology API independently having clean area of class 100000 ( ISO Class 8 ) and separate Isolator for different activities, managing all production team, meeting with targeted production, Sort out problems occurring during process operations, identifying areas of improvement and recommending for process modifications as per requirement, maintaining appropriate consumption of raw materials, Validation of new coming products for commercialization.

Taken lead for the commercialization of new coming products from R & D to production .

Planning and executing domestic and foreign customer audits in the plant.

Proper planning of raw materials and packing materials in close association with the purchase and stores department for the running products as well as new developed one.

Ensuring good house-keeping, responsible for maintaining proper safety in work and surrounding area.

Responsible for the preparation of SOP, responsible for the investigation of OOT, OOS, Change Control, responsible to find out the root cause of process deviation and taking corrective and preventive action (CAPA).

Responsible for the training of subordinates on the critical process operation, production related SOP and other plant related activities to run the plant safely and efficiently.

Responsible for Yield improvement, mass balance, energy balance calculation, WIP calculation.

Factory Head / Managing Director( CMD )

Calculating cost of the different products and applying cost reducing technologies to maintain the presence in the competitive market.

Job Achievement:

Completed validation of Fosfomycin Disodium, Erlotinib, Capecitabine ( USP/ IP ), Abiraterone Acetate, Pametrexed Heptahydrate,Tegafur for the commercial production .

Improved the quality issues in commercial batches of the Gefitinib and doubled the production of the same in the existing facility followed by process validation.

Improved quality and quantity of the commercialized Erlotinib, Capecitabine, Abiraterone Acetate and other ongoing products by monitoring the critical process parameters.

Reduced production cost of all the products by reducing batch time cycle and yield improvement.

Controlled all the operational issues and in lined the process engineering as per the requirement of the process.

2.Worked as a Manager Production in M/s Concord Biotech Limited, Ahmedabad (Gujarat),

A fast growing cGMP, USFDA, EU GMP and TGA approved facility engaged in the production of

Fermentation, semi synthetic and synthetic based APIs.

CA: Feb. 2014- April 2016.

Manager (Production)

Product: Anidulafungin, Ascomycin, Pimecrolimus, Teicoplanin (Injectable) etc.

Job Profile:

Leading and managing two manufacturing plants of multi product independently having clean area of class 100000 ( ISO Class 8 ) with Lyophilization facility and assisting other plants on technical issues, managing all production team, meeting with targeted production, Resolving the problems occurring during process operations, identifying areas of improvement and recommending for process modifications as per requirement, maintaining appropriate consumption of raw materials, responsible for the validation of new coming products.

Taken lead for the commercialization of new products developed in R & D/ Pilot to plant to plant scale.

Planning and executing domestic and foreign customer audits in the plant.

Proper planning of raw materials and packing materials in close association with the purchase and stores department for the running as well as new developed molecules.

Ensuring good house-keeping, responsible for maintaining proper safety in plant, maintaining records as per cGMP, preparing the production schedule and daily production report as well as monthly report.

Responsible for the preparation of SOP, responsible for OOT,OOS, Change Control, Deviation and taking corrective and preventive action (CAPA).

Responsible for the training of subordinates on the critical process operation, production related SOP.

Responsible for Yield improvement, mass balance, energy balance calculation, WIP calculation.

Reporting to GM Operation/Executive Director.

Calculating cost of the different products and applying cost reducing technologies.

Job Achievement:

Completed validation of Ascomycin and Pimecrolimus for the commercial production batches.

Completed the validation for the commercial production of Anidulafungin.

Taken lead for the development of batch at pilot plant scale to commercial production of Teicoplanin

for the commercial production.

3.Worked as a Sr Manager/Head Production and heading the entire production team of M/s Bakul

Pharma private Limited, Ankleshwar (Gujarat), a well known company having WHO, cGMP

approved facility engaged in the production of API and intermediates.

CA: Jan. 2011- Jan. 2014.

Sr Manager/Head (Production)

Product: Theobromine,3 Methyl-7 n-Propyl Xanthine, Pentoxyphylline, Doxophylline, Acephylline,

8 Benzyl Theophylline, Tertiary Butyl Benzene Sulphonamide, Proxyphylline, Dorzolamide etc.

Job Profile:

Leading all the production team, meeting with targeted production, stream lined operations, resolving problems occurring during process operations, Identifying areas of improvement and recommending for

process modifications .

Proper planning of raw materials and packing materials in close association with the purchase and stores department.

Responsible for the preparation of SOP, investigating for the root cause of process deviation and taking corrective and preventive action (CAPA).

Updation of documents like, SOPs, MPCR, BPCR and all GMP related records of the organization.

Responsible for the training of subordinates on the critical process operation, production related SOP and plant related activities to run the plant safely and efficiently.

Planning and executing domestic and foreign customer audits in the plant.

Ensuring the implementation & monitoring of cGMP functions as per ICH & WHO guidelines.

Ensuring good house-keeping, responsible for maintaining proper safety in plant, maintaining records as per cGMP standard and attending all the external customer audits, Preparing the production schedule and daily production report as well as monthly report.

Responsible for Yield improvement, mass balance, energy balance calculation, WIP calculation.

Reporting to Managing Director.

Job Achievements :

Streamlined operations, completed document as per GMP guidelines and implemented the same on shop floor in all the activities held under the premises, organized on line training programmes to avoid the mistakes in process/documents, producing significant gains in net earnings. Reduced RM consumption norms for Pentoxyfylline with improved quality and quantity.

4.M/s Solaris chemtech Industries, sister concern unit of Solaris Biochemical’s Ltd,Vadodara,

A well known company of Thapar group having ISO9001:2008, ISO14000:2004, OHSAS 18001:2007

approved facility engaged in the production API intermediates.

CA: 2003 – 2010

Sr Executive (Production)

Product: TBBA, BAB, AcBr, PNBBr, 1, 4 DBB, Bromo OTBN, PBFB etc.

Job Profile:

Ensuring plants desired production, maintaining appropriate consumption of raw materials.

Man power handling, managing for utmost utilization, ensuring good house-keeping in plant as well as surrounding area.

Trouble shooting of problems arising during process operation, maintaining records of all the batches,

Yield and mass balance calculation, Calculating norms for all the products and reducing it to meet the AOP.

Work closely with Pilot plant to take observation for the new incoming products developed in R & D during scale up in plant and planning for the product change over and modification of the plant as per new manufacturing process.

Ensure proper safety in work and surrounding area and maintaining records for the ISO audits.

Proper planning of raw materials and packing materials in close association with the purchase and stores. Preparation of the production schedule and daily production report.

5.M/s PI Industries Limited. Ankleswar, Bharuch (Gujarat) a group company of M/S Pesticides

India Ltd, having ISO9001:2008, ISO14000:2004,OHSAS 18001:2007 facility engaged in the

Manufacturing of fine chemicals.

CA :1999 - 2003

Production Supervisor

6. M/s Hiron Orgochem Limited,Panoli, (Gujarat) having GMP approved facility. It was one of the leading manufacturer of Ciprofloxacin in India.

CA : 1997 – 1999

Chemist (Production)

Product: Ciprofloxacin, Enrofloxacin, Levofloxacin.

7.Started career as a Chemist ( Trainee) with M/s K.A.Malle Pharmaceuticals Ltd, Ankleshwar, (Gujarat).

CA :1996 – 1997 as a Tr Chemist (Production)

Product: Mebendazole (White and off white)

Academic Background :

M. Sc (Organic chemistry) 1 st class from VBS Purvanchal University, Jaunpur (U.P) in 1995-1996.

B.SC (Chemistry) 2ndclass from VBS Purvanchal University, Jaunpur (U.P) in 1992.

Industrial Training:

Attended a full day training programme on First Aid organized by St John Ambulance Association.

Attended one day full Training programme on Accident Prevention Techniques organized by Gujarat Safety council (Vadodara).

One day full training programme on Preventing against Runaway reaction Organized by Chilworth Global PVT Limited.

Attended two days training programme on fire and explosion: A loss prevention approach organized by Prosafe process engineering PVT Ltd.

Personal profile:

Name : Vinod Chandra Chaubey

Father's Name : Shree Sakaldeep Chaubey

Date of Birth : 01-07-1970

Marital Status : Married

Passport No : K 4220315

Religion : Hindu(Brahmin)

Languages Known : Hindi, English, Gujarati, and Sanskrit

Present Salary : 13.0 Lacs /P.A ( CTC )

Salary Expected : Negotiable

Preferred Location : Baroda, Ankleshwar, Ahmedabad, Vapi, Everywhere in India.

NoticePeriod : Three months but negotiable on either side.

Declaration:

I solemnly declare that the details furnished above are true to the best of my conscience and belief.

Date :

Place : (Vinod Chandra Chaubey)

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