CURRICULUM VITAE

Pandia raj.P.

*/***-* *************,

Venkatachalapuram, Sattur (T.K),

Virudhunagar District-626203

. E-mail: adcc25@r.postjobfree.com

Contact No: +91-986*******

Experience Summary

Over 8+years of experience as a Production Chemist working extensively in Pharma industries for different client infrastructure projects. Seeking a growth-oriented technical position where I can contribute to the overall growth of the Organization. Highly Motivated, hardworking and dedicated. Good understanding of Production quality practices, good understanding and experience in working with team members from different cultures. Flexible enough to learn new things when required.

Worked as a Senior Executivein “MYLAN Laboratory Ltd. US FDA Regulatory Plant’’ (Aseptic Preparation).

Authority for BMR Approval Signature – COMPENTENT TECHNICAL; STAFF SIGNATURE

PROFESSIONAL SUMMARY

PREVIOUS EMPLOYMENT

Organization: MYLAN LABORATORY LTD-US FDA REGULATORY PLANT. Bangalore.

(An US FDA Regulatory, EU, MHRA, & ISO facility approved pharmaceutical formulation unit for liquid Injectable, manufacturing small volume Parenteral.)

PERIOD: OCT 2015-JUN 2019(3 years 8 months)

Designation: Senior Executive

PREVIOUS EMPLOYMENT

Organization: HETERO LABS -US FDA REGULATORY PLANT. Hyderabad.

(An US FDA Regulatory, EU, MHRA, & ISO facility approved pharmaceutical formulation unit for liquid Injectable, manufacturing small volume Parenteral.)

PERIOD: DEC 2014-OCT 2019(10 months)

Designation: Senior Executive

PREVIOUS EMPLOYMENT

Organization: - KEMWELL BIOPHARMA PVT LTD US FDA REGULATORY PLANT. Bangalore.

(An US FDA Regulatory, EU, MHRA, & ISO facility approved pharmaceutical formulation unit for liquid Injectable, manufacturing small volume Parenteral.)

PERIOD: OCT 2013-DEC 2014(1 year 2 months)

Designation: Executive

PREVIOUS EMPLOYMENT

Organization:. GLOBAL PHARMA TECH PVT- Hosur.

(EU, MHRA, & ISO facility approved pharmaceutical formulation unit for liquid Injectable, manufacturing small volume Parenteral.)

PERIOD: OCT 2010-SEP 2013(3 years 1 months).

Designation: Senior Executive

EDUCATIONAL QUALIFICATIONS:

Bachelor Of Pharmacy – 2003 to 2007

Master Of Pharmacy - 2008 to 2010

KEY ROLES - RESPONSIBILTIES:

Making batches and conducting stability studies for new products as per guide lines.

Carrying out packaging development.

Maintaining all equipment and records as per guidelines.

Writing and issuing product development reports.

Developing specifications and other documentation for new products.

Assisting in technology transfer from R&D to production.

Providing manufacturing support for established products

Knowledge of pharmaceutical ingredients, manufacturing processing equipment’s, and testing equipment’s.

The ability to coordinate with team members regarding multiple drug delivery systems.

Understanding of chemical and physical properties of active ingredients.

Knowledge in scientific principles and regulatory requirements for pharmaceutical development.

Every One Hour checking the Fill volume, Sealing, Height, Clarity as per guidelines.

Every Two Hour checking the Washing Clarity for both Ampoules and Vials.

Every Two Hour checking the Differential Pressure and Temperature.

Validations Like,

* Autoclave & DHS,

* Equipment Validation,

* Area Validation,

* Utility Validation etc...

Documentation and implementation of cGMP and SOPs of all related areas.

Executing Validation Activities at the site with the support external agencies where applicable.

Carry out level -1 and -2 self-inspections.

Training of Production operators, Staffs’

Review of BMR.

Ensure Documentation of Deviation\Change Control.

Support for Audits.

Daily planning to meet the Production target and scheduling.

To plan Production activity as per the Production schedule.

To plan man power requirement.

Executing Formulation, Washing, Sterilization, Aseptic Filling, Inspection activities.

To co-ordinate with engineering Department and ensure that the Preventive maintenance of all machineries are done on planned preventive maintenance day.

To ensure discipline line in manufacturing Filling and Inspections.

To ensure all the employees are following cGMP at every stages of Production activity.

To ensure better yield and maximum Productivity.

To run the department in a cost effective manner.

Co-ordination with related Department for effective execution of Production schedules.

To train the employees on Aseptic work culture and monitor all the involved employees are following the aseptic work culture.

To raise deviation repots and change controls, as applicable.

To ensure proper housekeeping in to the department.

HANDLING OF EQUIPMENTS:

ROMACO & BOSCHVIAL FILLING & SEALING MACHINE

ROMACO &BOSCH VIAL WASHING MACHINE

PETALS VIAL FILLING & SEALING MACHINE

PETALS VIAL WASHING MACHINE

PETALS AMPOULE FILLING MACHINE

PETALS AMPOULE WASHING MACHINE

ADAMS LYOPHILIZER MACHINE

CADMAC AMPOULE FILLING MACHINE

BHUVANESWARI VIAL WASHING MACHINE

PHARMALAB AUTOCLAVE

KLENZAIDS VIAL WASHING MACHINE

ACHIEVEMENTS:

US FDA AUDIT,

MHRA AUDIT,

EU @ ISO AUDIT.

EXTRA-CURRICULAR ACTIVITIES:

Doing N.S.S Champ at MADURAI-MEENAKSHI MISSION Hospital (2006).\

PERSONAL PROFILE

Father’s Name : S.Paul raj

Date of Birth : 16/10/1986

Sex : Male

Nationality : Indian

Religion : Hindu

Marital Status : Single

Languages Known : Tamil, English, Telugu, Kannada, and Hindi

Hobbies : Reading books & Music’s

Permanent Address : 4/471-B Bharathinagar,

Venkatachalapuram, Sattur (T.K),

Virudhunagar District-626203

REFERENCES:

1)Mr. Pankaj- ProductionAsst.Manager Heterolabs Ltd.Ph.No.998-***-****

2)Mr.P. Manohar-Production Senior Manager Hospira Ltd Chennai.Ph.No.971-***-****

Declaration

I hereby declare that the above information furnished is true to the best of my Knowledge

Place: Sattur Signature,

Date: (PANDIA RAJ.P)

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