No.49/A, Sri Chakra Thazhuvar Salai,: R.Bhupathy. SR - Executive - Sterile & Non Sterile Drugs Manufacturing

Curriculum Vitae of Ramshah Bhupathy.
R.Bhupathy. No.49/A, Sri Chakra thazhuvar salai,

Sr.Executive – Sterile & Non Sterile Drugs Manufacturing Eari Sai ram nagar,
Madurantakam,
Kanchipuram district - 603306.
E: [email protected].
Mobile No:+91800863479.
Career Objective
Intend to build a career with leading corporate of Pharmaceutical Manufacturing with committed
and
Dedicated people, which will help me to explore myself fully and realize my potential. Willing to
work
As a key player in challenging & creative environment.
Academic Chronicle
 M.Sc., Chemistry
Master of Science - Chemistry (2017-2019),
Chennai affiliated to University of Madurai Kamara jar.
 Diploma In Chemical process and Instrumentation control ( 2005-2006)

Annamalai University – Chidambaram.
 B.Sc.,
Bachelor of Science- Chemistry (1995-1998) from Arraigner Anna govt, art’s & science
College, Villupuram.
Chennai affiliated to University of Madras.
 H.S.C.,
Higher Secondary Certificate (1993-1995) from Tamil Nadu Board.
Work Experiences
From December 2007 to Till Date
a. Designation : Executive - Production Sterile

Sterile - Lyophilizes facility & crystalline facility.
b. Organization : M/S Orchid Chemicals & Pharmaceuticals Ltd.,
Chennai, Tamil Nadu, India. As known currently
Orchid pharma limited.
c. Organization Profile : Manufacturers of Cephalosporin’s,
ISO 9001: 2000, 14001 & US FDA, MHRA, TGA certified
Manufacturing facility.
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From April 2006 to Januvary2007.

a. Designation : Production Chemist. Non – Sterile products
b. Organization : M/S Sun Pharmaceuticals limited,

Madurantakam, Tamil Nadu, India.
From August 2000 to April 2006.

a. Designation : Analytical cum production Chemist.
Manufacturer of linear alkyl benzene sulphonic acid (Acid slurry)
b. Organization : M/S Anand Chemicals as known currently Vasanth chemicals

Thirubhuvanai, Pondicherry, India.
Job Profile
Duties and responsibilities:

 Responsible for safety in the Manufacturing area.
 Training the personnel for SOP, validations, cGMPs.
 Motivating the personnel. Utilizing of manpower in the shop floor.
 Production scheduling as per the production plan.
 Resource planning – Men and Material.
 Inventory control at the plant level.
 Control of Aseptic operations.
 Review of Documents related to aseptic operations.
 Maintain Class 100, 10000 and Class 100000.
 Preparation and review of Standard Operating Procedures.
 Complying with the cGMP requirements.
 Reporting the Productivity, Performance of the plant to the Top Management.
 Implementing the Master Validation Programme.
 Performing Sterilization Process Validations of Equipment’s.
 Execute validations as per the protocols.
 Trouble shooting & problem solving.
 Preparation, Maintenance and Review of Documents related to ISO and cGMPs.
 Regular quality review of analytical results of products produced.
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 Co-ordinating with other interrelated departments to achieve the production target.
 Known for distillation process in reactor and distill column units.
 Lyophilizer trial batches for process development formulation LYO unit handled.
 Both API and formulation plant operations and documents handled.
Validation Experience
 Steam Heat Sterilizer Validation:
 Heat Distribution study and cold point detection.
 Heat Penetration Study with Maximum and Minimum Load.
 Review of validation documents.
 Dry Heat Sterilizer Validation:

 Heat Distribution study and cold point detection.
 Heat Penetration Study with Maximum and Minimum Load.
 Sterilization Process Validation:

 Heat Distribution study and cold point detection in Reactor,
Aseptic Filtration System and Blenders.
 Process Simulation Validation using Lactose:

 Aseptic Process simulation using Lactose.
 Training of personnel for process simulation studies.
 Process Validation of Sterile Drugs:

 Holding Time Study of the Sterile Drugs.
 Concurrent Process Validation of the Sterile Drugs.
 Sterilized tools and Garments Storage:

 Storage Time Study for the Sterilized tools and Garments with the help of
Microbiology.
 Disinfectant Solution Validation:

 Effective dilution and usage frequency validation with QC Microbiology.
 HVAC System Validation:

 Integrity of the System, Cleanliness level monitoring and Uniformity
checking in the area.
 Velocity and Air-changes calculation for the Clean Rooms.
Page 3 of 4
Strengths
 Ability to lead, motivate, and develop others
 Hard working, Energetic and Ambitious.
 Perseverance and self-motivated to achieve the set targets.
 Team building
 Flexible and optimistic
Personal Details
Name of Father : R. Mani

Name of Mother : M.Krishnaveni
Date of Birth & Age : 24-11-1978 & 40 years
Sex : Male
Marital Status : Married.
Nationality : Indian.
Passport Number : G8860342
Languages known : Tamil, English & Hindi.

Computer Knowledge : MS-office, SAP basis.
Date: (R.Bhupathy.)
Page 4 of 4

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Curriculum Vitae of Ramshah Bhupathy.

R.Bhupathy. No.49/A, Sri Chakra thazhuvar salai,

 Diploma In Chemical process and Instrumentation control ( 2005-2006)

From December 2007 to Till Date

a. Designation : Executive - Production Sterile

From April 2006 to Januvary2007.

b. Organization : M/S Sun Pharmaceuticals limited,

From August 2000 to April 2006.

b. Organization : M/S Anand Chemicals as known currently Vasanth chemicals

Duties and responsibilities:

 Dry Heat Sterilizer Validation:

 Sterilization Process Validation:

 Process Simulation Validation using Lactose:

 Process Validation of Sterile Drugs:

 Sterilized tools and Garments Storage:

 Disinfectant Solution Validation:

 HVAC System Validation:

Name of Father : R. Mani

Languages known : Tamil, English & Hindi.

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