Resume CV : Plant head pharma production

[arvindmodi1955]

RESUME :
ARVIND.P. MODI
E-mail- arvindmodi1955 AT yahoo.co.in

SUMMERY :
More than 30 Years experience in Pharmaceutical Industry , The experience includes Pharmaceutical Manufacturing , Product Development , CGMP , Quality Assurance , Regulatory Affairs & Laboratory Operation.

EXPERIENCE :
1. PRESENT EXPERIENCE :From 23/11/2009 working as a senior manager(plant)RATNAMANI HEALTHCARE PVT LTD AHMEDABAD directily reporting to director looking after all activity of formulation plant.having of tablet, capsules, oral liquids, Oral Powder dept. & Q.C Dept.
2. From Nov 2007to22nov,2009 working as a Works Manager with Maan Pharmaceuticals Ltd , Mehsana .
- Maintain the Audit Programmed, Internal Audit, Sub Contractor Audit , Establishing & Maintaining Audit standards as per the regulatory & Company requirements.
- Create revises , review & approves SOPs for dept. & other area . Review and approves validation protocols
- Demonstrate excellent written & verbal skills with ability to communicate clearly & effectively with colleagues. Also demonstrate ability to work with multi disciplinary teams
- As a management representative & General Manager Production, lead the TEAM to obtain WHO GMP certificate & ISO 9002 certificate.
- Establishment of tablet, capsules, oral liquids, Injections, Ointment & Oral Powder dept. & Q.C Dept.
- FDA approval in tablets, capsules, Injections, Ointment & Q.C Dept.

3 Name of the Organization : M/s. Leamak Healthcare Pvt. Limited.
Company Profile : Leamak Healthcare Pvt. Limited is an ISO 9001 company , which manufacturing and exporting , Throat Lozenges , Confectionery items for reputed company , i.e. Rickitt , Shreya , Genom , Boots Piramal & ITC Limited.
JOB PROFILE :
Since 1st April 2003 to Oct 2007, working as a General Manager with M/s Leamak Healthcare Pvt. Limited situated at Matoda Sarkhej Bavla Highway and looking after production of Lozenges for reputed companies like Rickitt , Shreya , Genom , Boots Piramal & ITC Ltd.
- Maintain the audit program, Internal Audit, Sub Contractor Audit, Establishing & Maintaining Audit Standards as per the regulatory and company requirements.
- As a management representative and General Manager Production, lead the TEAM to obtain ISO 9002 certificate.
- Applied practical & theoretical knowledge to improve the capability of the laboratories.
- Also work closely with customers in manufactures & quality control to help to collect the necessary data to investigate & resolved the production problem.
- Create revises, review & approves SOPs for dept. & other area . Review and approves validation protocols
PREVOIUS EXPERIENCE

4 Since December 1991 to March 2003,
worked as a General Manager Production : Maan Pharmaceuticals Ltd , Mehsana .
- Maintain the Audit Programmed, Internal Audit, Sub Contractor Audit, Establishing & Maintaining Audit standards as per the regulatory & Company requirements.
- Create revises, review & approves SOPs for dept. & other area. Review and approves validation protocols
- Demonstrate excellent written & verbal skills with ability to communicate clearly & effectively with colleagues. Also demonstrate ability to work with multi disciplinary teams
- As a management representative & General Manager Production , lead the TEAM to obtain WHO GMP certificate & ISO 9002 certificate.
- Establishment of tablet , capsules , oral liquids Injections , Ointment & Q.C Dept & Oral Powder dept.
- FDA approval in tablets , capsules , Injections , Ointment & Q.C Dept .

5 Since August 1990 to November 1991
worked as a Production in charge : Alps Laboratories Limited , Mehsana.
- Looking after production of Tablets & Capsules in latest blister pack machine, Compression Machine , FBD Machine & RMG.

6 Since August 1989 to August 1990
worked as a Senior Chemist : EU Pharma Laboratories , Ahmedabad
Looking after production of Tablets & Capsules including Sugar & Film coating

7 Since January 1987 to August 1989
worked as a Manager Quality Control : Morvell Laboratories Pvt. Limited , Mehesana .
a. Active participation in setting up air handling system , air cooling system , & production facility for small volume parenteral & Q C Dept.
b. Also work closely with customers in manufactures & quality control to help to collect the necessary data to investigate & resolved the production problem.
c. Applied practical & theoretical knowledge to improve the capability of the laboratories.

8 Since August 1984 to December 1986
worked as a Production In-charge : B.P CO. (Kandla ) Export , Kftz.
d. To prepare export documents & manufacturing of oral powders , tablets , Capsules for large scale export.
e. Import / Export procedure at Kandla free Trade zone for export of Pharma Products to Russia.

9 Since August 1978 to August 1984
worked a Production Chemist : Suhrid Giegy Ltd., Baroda
Looking after small volume inject able production & preparation of BMR , batch Manufacturing , filling , maintenance of sterile area.

10 since September 1977 to July 1978
worked as Analytical Chemist :Alembic Works Co. Limited , Baroda
a. Handling phisico chemical testing of R.M. & Finish products.
b. Performs instrument analysis U.V , GC , HPLC & Flame photometry of in process & finish pharmaceuticals formulation.

EDUCATIONAL QUALIFICATION :
1. B.PHARMA from L.M. Pharmacy, Ahmedabad in 1977.
2. LLB from Gujarat University in 1983.

PERSONAL DETAILS :
Date of Birth : 10th August 1955
Marital Status : Married
Language Known : Gujurati , Hindi & English

ARVIND.P. MODI

[Guest]

Attn :Human Resources Recruiter,
Sub : Application for the post of Manufacturing Department

Dear Sir / Madam,
I am very much enthusiastic to work in your Production Department. I have a Bachular in Pharmacy form SGRRITS Dehradun which has been accredited by the Garhwal university
I have 6 years of experience in Manufacturing and Packaging of Tablets andCapsules Formulations, in WHO GMP approved Organizations. Approved in tablet from uttrakhand FDA
My success in the past has stemmed from a strong commitment to hard work; sense of professionalism, dedication any responsibility. I am sure that my strong background and related work experience will enable me to meet the demands of the position and allow me to apply my knowledge.
Thank you for taking time to review my application and I appreciate your consideration and look forward to hearing from you shortly.

Yours truly,
Rajesh Singh

Curriculum Vitae:
Rajesh Singh
rashmi.ramola AT gmail.com , ramolarajesh AT gmail.com

CAREER OBJECTIVES :
To effectively utilize my professional abilities to obtain a challenging position in Pharmaceutical Industry.

SUMMARY :
Skilled Professional having Six years of experience in Manufacturing and Packaging of various Pharmaceutical dosage forms viz., Tablets, Capsules and powders and in WHO, GMP approved Organizations.

EDUCATIONAL QUALIFICATION : B. Pharma from Shri Guru Ram Rai Institute of Technology and Science, Dehradun affiliated to Garhwal University, Srinagar, Uttarakhand, approved by A.I.C.T.E & P C I.

COMPUTER SKILLS :
- One Year computer Diploma in DISM from APTECH Dheradun.
Working in ERP

EXPERIENCE :
CURRENT JOB STATUS :
Working in Tablet & Capsule Department in WINDLAS HEALTHCARE(P) Ltd., Dehradun, WHO- cGMP Certified Plant from Apr. 2010 to till date.(As assistant manager)

PREVIOUS WORK HISTORY :
Two year Exp. in ELDER PHARMACEUTICAL Ltd. From Nov 2007 to 11 Jan 2010 Selaqui Dehradun, a WHO- cGMP Certified Plant (Production chemist)
- Two year Exp. in Bhavishya Pharmaceutical Pvt. Ltd. Unit Ist Hyadrabad from Aug. 2005 to Oct. 2007 (Production chemist)

AUDIT FACED : Pfizer, Ranbaxy,GlanMark, UCB, Abott. Mili healthcare etc

FIELD OF INTEREST : Production (in granulation compression & Coating Section).

SKILL :
- Manufacturing of Tablets, Capsules.
- Process Validation
- Calibration of Measuring Devices & IPQC Apparatus
- Updating of BMR, BPR & SOP’s related documents & maintaining them.
- Production Planning(Monthly and weakly)
- A dedicated and highly motivated team player.
- Quick learner and easy adaptability to new methods and systems.
- Good Understanding of cGMP.

Current Responsibility :
Being an in charge of Tablet and Capsule section, I have total responsibility of all shop floor activities from Dispensing Granulation to coating of Tablet as well as from Granulation to filling of Capsule with a team of chemist, operators and helpers.
Involved in different processes of Solid Drug Dosage production development cycle like Dispensing of active and non-active Raw materials, Sifting, Granulating,Blending, Milling, Tablet compression, looking after troubleshooting, stage wise yield calculation, label and weigh finished products as per Sop’s.
Involved in Cleaning, Setting and Operating of various machines and rooms according to Standard Operating Procedures (SOP’s).
Responsibility to produce products with a consistent quality and to give maximum output from all sections with in a frame of quality (cGMP).
Responsibility to follow cGMP my self as well as educate my sub- ordinates to follow.
Responsibility to make weekly schedule and shift schedule as per production target and to ensure its implementations.
Responsibility to maintain healthy work of mind, discipline and teamwork among those who are working under me on shop floor.
Maintain various PBR(production batch record), reconciliation records,in-process check records Responsibility to keep B.M.R, B.P.R, machine logs and other related production documents up to dated in all respects. Maintained various documents i.e. machine log books, temperature and
humidity records, differential air pressure records, digital balance checking, area cleaning records, sieve inspection records, die punch inspection records etc.
Responsibility to inform maintenance department in advance for due of preventive maintenance of all shop floor machines.
Responsibility to give all section wise reports to Production manager/General manager.
Responsibility to give optimum yield from granulation, compression, coating & capsule filling.

MACHINES KNOWLEDGE :
- RMG, FBD, PLM, OCTAGONAL BLENDER , MULTI MILL, OSSILATING GRANULATOR, VIBROSIFTER, & MATERIAL HANDLING DEVICE IN GRANULATION AREA.
- COMP 45stn, 35 stn , 27stn 20stn 29stn 35stn and 37stn Bilayer IN TABLET SECTION & ROLLCOMPACTOR
- AUTOCOATER (26” 37” 42” 60”. 66”. 48”. & Coating Pan 48 “), COLLOID MILL, MECHANICAL STIRRER IN COATING AREA.

QUALITIES :
Working experience in a correct designed / lay out plant, (From material receiving by store to material dispatch by production.)
Making plan for giving maximum output with quality by utilizing optimum manpower in less extra time.
Ability to develop a skill & perfect operator from a raw person.
Practical knowledge in operation of all cGMP modeled machines in prod.
Already work in a WHO Approved Company.

ROLE & RESPONSIBILITIES :
Ability to handle Manufacturing Unit.
Ensure attainment of production targets with quality.
Making innovative efforts to strengthen and boost up the factory activities by creating an enterprising atmosphere leading to improving overall efficiencies of manufacturing & maintaining discipline.
Responsible for all manufacturing operations, control over wastage, spoilage, staff discipline, interaction and co-ordination between purchase and store Production Planning Monthly and weakly

I would like to share the knowledge present the concept precisely, explore the knowledge & learn about the technology those will help me to
grow my self & help the organization to grow also.

Place :- (RAJESH SINGH)
Date :-