The document is a cover letter and resume from Amar Borate applying for an Assistant Production Manager position. He has over 12 years of experience in API manufacturing, process development, and quality assurance. Currently he works as an Assistant Manager at Watson Pharmaceuticals with responsibilities like production planning and documentation, handling shifts, and ensuring FDA compliance. He is seeking a new position where he can further contribute to organizational goals in a global company.

1. To,
Human Resources
Subject: Application for the post as Asst. Production Manager / Manager in API BULK DRUG
Manufacturing.
Dear Sir,
With reference to your requirement, I Amar J Borate would like to apply for the same as above mentioned
in light my educational qualification and Industrial experiences in various organization.
As a competent professional with around twelve plus years industrial experience in manufacturing in Active
Pharmaceutical Ingredient in various reputed organization, handling of more than 30 regulatory API.
I am young dynamic person of age 34 years, education qualification Msc from Dr. Babasaheb Ambedkar
University, Aurangabad, Maharastra.
Currently working with Watson(Actavis) Pvt. Ltd. Ambernath as Asst.Manager Production
manufacturing API, from 14th April 2014 to till date. Taking care of various departments Manufacturing &
Process, In process quality control & Planning Management.
Watson(Actavis) Pvt Ltd is MNC unit with United States Food Drug Administration (USFDA) and
World Health Organization (WHO) approved facility.
I feel much obliged, if you give me chance to serve in your esteemed organization, will try my best level to
perform in respect of organizational goal in Global presence.
All information is given in CV is correct in best my knowledge.
Enclosed herewith CV.
Expect your favorable reply and with best regards
Amar Borate

2. AMAR JEHANGIR BORATE
Contact: +91-9975949691 ~ +91-7776810051 ~ E-Mail: amarborate21@yahoo.co.in
Seeking assignments in the domain of Production Management with an organisation of high repute, preferably
in Pharma sector
PROFILE SUMMARY
 USFDA Certified Professional with nearly 12 years experience in Production Management, Product
Development, Process Improvement, Quality Assurance and Shift Management Activities
 Good leadership quality and team player, Good communications and presentation skill.
 Well versed with SAP activities, ICH Guidelines, AHU System & Pharma Cleanroom Concepts, Truly DCS
operation.
 Handled commercial manufacturing plants & achieved the manufacturing set target.
 Standardization of process of Active Pharmaceutical Ingredient with commercial viable, with Yield, Quality
and Safety as per Pharmacopoeias Standards with cost effective process
 Proficient in developing & streamlining systems with proven ability to enhance operational effectiveness
and meet operational goals within the cost, time & quality parameters
 Expertise in conceptualizing profitable production operations encompassing procurement, quality and
industrial relations
 Adept in enhancing production process operations, optimizing resource utilization, escalating productivity
and operational efficiencies
 Possess strong research, analytical, problem-solving and interpersonal communication skills
CORE COMPETENCIES
 Coordinating with various functions, ensuring optimum utilization of resources and implementing quality
management systems
 Handling process related activities and liaising with project team and consultants
 Programming, planning and executing raw materials, production and delivery activities
 Overseeing production of various drugs & implementing plans with a view to ensure timely
accomplishment of production targets within the cost parameters
 Investigating unusual / unacceptable results, process validation & cleaning validation samples, monitoring
in-process, blend analysis and reaction monitoring samples
 Formulating standard operating procedures for new processes / equipment for ensuring environment,
health & safety aspects
 Managing product development customization functions including requirement analysis, finalizing
specifications, designing, prototype development & testing activities
 Preparation of cGMP related document.
 Manufactured multiproduct in carrier.
 Preparing of GMP document like BMR, SOP, etc.
 Knowledge of TPM.
 DuPont training on safety completed.
 Track wise training, Deviation, Change control filling.
ORGANISATIONAL EXPERIENCE
Since April 2014: Watson (Actavis) Pvt Ltd., Ambernath as Asst.Manager Production
Role:
 Liaising with Q.C, Q.A, Engineering, Warehouse and EHS Departments
 Preparation of GMP related documentation such as BMR, SOP, End campaign report, etc.
 Filling of deviation, Change control online, training,.
 Handling Plant , manpower & its related activities.
 Handling shift activities and devising:
o Production documents of API batch
o Optimized and safety flow sheet of different product manufacturing processes
o Critical process parameter with help of R & D Department

3. o Process validation data
o Safety training.
o DCS operation
o Trouble shooting related to process
o Multi product handled.
o Planning of production Vs execution with yield and quality, cost with safety aspects
o Investigate OOS, deviation and implement effective CAPA for non-conformance
o People development, training and skill up gradation
 Reducing batch cycle time and conducting USFDA audits
 Reporting to Dy General manager
 Knowledge of SAP transaction
 Training to sub-ordinate of process, cGMP, Safety
 Familiar with AHU & Clean room concept
 Implementation of production planning
 First Aider Safety squad member
 Knowledge of TPM.
Accomplishments:
 Sampling point modification.
 DCS operation training to new associate.
 Operation without opening manhole removing the sample from reactor, ANFD dryer troubleshooting solved
by discussion & implementation with co-ordinating with sub-ordinate & superior
 All process i.e. unit operation are carried out in closed system without any opening of reactor, receiver
,dryer manhole for mean of safety
Jun’10-April `14: Sandoz Pvt. Ltd., Mahad as Executive-Production
Role:
 Liaising with Q.C, Q.A, Engineering, Warehouse and EHS Departments
 Preparation of GMP related documentation such as BMR, SOP, End campaign report, etc.
 Filling of deviation, Change control online.
 Handling Plant & its related activites.
 Handling shift activities and devising:
o Production documents of API batch
o Optimized and safety flow sheet of different product manufacturing processes
o Critical process parameter with help of R & D Department
o Process validation data
o DCS operation
o Trouble shooting related to process
o Multi product handled.
o Planning of production Vs execution with yield and quality, cost with safety aspects
o Investigate OOS, deviation and implement effective CAPA for non-conformance
o People development, training and skill up gradation
 Reducing batch cycle time and conducting USFDA audits
 Reporting to Dy General manager
 Knowledge of SAP transaction
 Training to sub-ordinate of process, cGMP, Safety
 Familiar with AHU & Clean room concept
 Implementation of production planning
 First Aider Safety squad member
 Knowledge of TPM.
 Dupont training on safety completed.
Accomplishments:
 Cloth pad instead of paper pad in commercial production
 DCS operation training to new associate.
 Operation without opening manhole removing the sample from reactor, ANFD dryer troubleshooting solved
by discussion & implementation with co-ordinating with sub-ordinate & superior

4.  All process i.e. unit operation are carried out in closed system without any opening of reactor, receiver
,dryer manhole for mean of safety
Jun’06-Jun’10: Emcure Pharmaceuticals Ltd., KurKumbh as Production-Officer (Shift In-Charge)
Accomplishments:
 Received:
o First Prize in Safety Competition in 2006
o First Prize in Safety Competition in 2007
 All manual system runned on full occupancy without any major accident & high productivity
 As plant was new multi-product facility set up of new products many of troubleshooting occurred & solved
as line tracing problem, leakages, filtration problem, equipment suitability, new manpower, documentation.
PREVIOUS EXPERIENCE
Feb’06-Jun’06: CIPLA Ltd., Kurkumbh as Shift In-Charge-Production-Officer
May’02-Jan’06: Orchid Chemical & Pharmaceuticals Ltd., Waluj, Aurangabad as Assistant Production Officer
Accomplishments:
 Received an award for:
o Fire Fighting
o Rendering safety suggestions
 Successfully started new plants and made them completely functional
EDUCATION
2002 M.Sc. (Industrial Chemistry) from Azad College, Dr. B.A.M.U. Aurangabad. Secured First Class
2000 B.Sc. (General Science) from Dr. B.A.M.U. Aurangabad
Additional Qualification:
Year 2012 C.C.C.O. from B.T.E., Mumbai
Year 1995 Advanced Diploma in Computer Software and Analysis from yashshree Infotech, Osmanabad
Year 2012 Certification Course on Systematic Approach to Managing Process and Power Handling Hazards
from institute, Mahad
IT Skills: Well verses with Windows, MS-Office (Word, Excel and PowerPoint) and Internet Applications.
PERSONAL DETAILS
Date of Birth: 15th October 1978
Permanent Address: Amar J. Borate, Shubhamkar Complex, M.G. Road, Mahad, District-Raigad, state-PIN
402301
Languages Known: English, Hindi & Marathi
References:-
G.L.Patil:- Production AGM in Emcure Pharmaceuticals Ltd.
Kurkumbh, Pune Mobile No.- 09371776750.