Quality Control Assurance

CURRICULUM VITAE

Professional Objective:

Diligent and Result oriented professional with ability to work in team spirit and integrate the twin fundamentals of quality assurance and control; currently spearheading with ADCOCK INGRAM PHARMA, BANGALORE as Asst.Manager of IPCQA, Manufacturing Dept .

Involved in Audits like, TGA, UK, cGMP, other Customer and Internal Audits. Expertise of Good Laboratory Practices in Quality Control Measures.

Good organizational and analytical skills, Confident, Self-motivated independent. Problem solving attitude, team spirit and always willing to learn.

Attend the all Internal trainings like fire fighting, ISO, cGLP & cGMP…etc

Attend to FIRST AID, Fire fighting training trainings

Attend to Fire fighting Attend to ISO-9001, ISO-14001, cGLP & cGMP training

Computer knowledge: MS-Office, Windows, Oracle, ERP, SAP Implementation.

Experience: Caliber BRM

Qualification:

M.Sc organic chemistry and industrial chemistry

SSC 1989 MUNICIPLE HIGH SCOOL 55%

INTERMEDIATE 1992-1994 SREENIVASA JUNIOR CILLEGE 50%

BSC 1995 - 1996 botany zoology chemistry scnr govt college 58%

M.sc 1996 - 1997 in organic chemistry Bhopal university 55%

M.sc 1997 - 1998 in industrial chemistry Bhopal university 62%

Work experience:

I have 15 years of experience in Quality control Dept.

I Presently Working as a Managing Staff at Kevis Labs Pvt. Ltd. At Ongole 2019 to till date

I worked as Managing staff QC& Formulation development ADCOCK INGRAM PHARMA, BANGALORE Telagana state Feb 2017 To 2019 (formulation unit)

I worked as Management staff - QC, Apothecary pharmaltd, Hyderabad, Andra pradesh. Since April 2010 to may 2012 (Active pharma ingrient )

I worked as Executive – QC and AR&D in Montajat vetenary pharmaceuticals ltd, Dammam, Saudiarabia. From August 2007 to July 2009 (formulation unit)

I worked as officer - QC in Natco pharma LTD, Hyderabad, Andhra pradesh. From April 2005 to July 2007(formulation unit)

I worked as Chemist - QC in Aurobindo Pharma LTD, Hyderabad, Andhra pradesh. From May 2003 to May 2005(active pharma ingrient)

Job Responsibilities:

Preparation of all Validation documents for Protocols, Test data sheets, Summary &

Conclusion reports like, Cleaning validation, Method validation &

Method verification

To Review of all Validation, In process, Intermediate, Finished Products documents of HPLC, GC & Chemical analysis.

Planning & execution of Validation of Day to Day activities and reporting to Section Head

To ensure the periodic Calibration & Maintenance of HPLC,GC, UV Spectro photometer, IR Spectro photometer & Other Chemical Analysis Instruments

To ensure the Out of Specification & Out of trend of analysis Like Analyst errors and Instrument errors

To ensure the Stability analysis of all Conditions like Long term, Intermediated and Accelerated

Working on succession planning of the workforce, shift management activities, appraising the member's performance & providing feedback.

Present now clinical trials

Analytical Method development/optimization

Timely delivery of results

Method transfer and coordination with production sites

Trouble shooting the problems associated with analysis, instruments etc.,

Planning and execution of shift activities.< BR>f. GLP & GMP compliance

Subordinate development.

The most critical challenge is to develop the cost effective analytical methods for new raw materials, formulations and intermediates in time with minimum trials and to deliver the result on time with consistency. GLP and GMP compliance with appropriate documentation Trouble shooting in analysis and coordination with production sites

Handling of HPLC (High performance liquid chromatography) GLP (Gas liquid chromatography) and NMR (Nuclear magnetic resonance) QA Line for documentation and protocols and quality management systems. Vetenary vaccine and injection also experience in microbiology analysis of LAL test for progenies.

COMPETENCY

Good analytical skills

Problem solving kills

Effective business communication

Customer focus results oriented knowledge skill

Caliber of BRM software used

RESPONSIBILITY / AUTHOROTIES: IPCQAM

Handling of Instruments & Software’s like:

Auto titrator and K.F. Titrator – (Metrohm-794 & 795)

U.V. Visible spectrophotometer – (Shimadzu UV-1601, UV-1800).

Polari meter – (Jasco-P-1020, P-2000)

FT-IR Spectro Photometer – (Perkin Elmer-Spectrum one).

High performance Liquid Chromatography:

Waters 2695 Empower-II

Agilent-1100, 1200 series E.Z Chrome & Chromeleon

Shimadzu LC 2010 AHT & PHT

Gas Chromotography: Agilent 6890N,

Atomic absorption spectroscopy (AS-201)

LC-MS analysis

Total organic Analyzer (TGA-7

Personal Profile:

Name of the candidate : R.viswanath Reddy

Father’s Name : R.P.Sidda reddy

Date of Birth : 10-10-1973

Sex : Male

Marital Status : Married

Religion : Hindu

Native Place : Kadapa, A.P

Address for Correspondence : R.Viswanathreddy

Buddaipalli

Proddatur-516361

Kadapa(Dist)

Andrapradesh state

Place:

Date: (R.viswanathreddy)

R. Viswanath Reddy Mail:****************@*****.***

Cell No.:944*******

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