Manager Quality Control

Resume

A-**, Nangloi, Phase-*, Delhi-**

Phone: 971-***-****

Email: pjlv89@r.postjobfree.com

QAIS MALIK

Professional Qualification

1. M.Sc in Bioinformatics from Jamia Millia (JMI) New Delhi with Ist Division (2005)

2. Bachelor of Science with Chemistry, Botany, Zoology from Delhi University, New Delhi with IInd Division.(2002)

Work Experience

Around 6 years of experience in Pharma Industry (Formulation unit and Analytical Research) in quality control deptt.

Current profile

Presently working as Asst. Manager Global Lims Operations with iGATE Global Computers Systems, Noida.

• Working as Global LIMS Master Data Analyst

• Method Developer on Sample Manager (LIMS Software)

• Creating Analytical Calculation Sheets

• Validation of Analytical methods on Sample Manager.

• Interacting with clients for method up gradations on LIMS

• Application Development of Sample Manager

Previous employer

• Worked with Kusum Healthcare Pvt. Ltd, (Bhiwadi; Rajasthan) as Q.C. Analytical Chemist from Oct 06 to April 08.

• Analysis of semi-finished goods through HPLC.

• Analysis of finish & stability products through HPLC.

• Knowledge of Validation and Calibration of different analytical methods and Instruments

respectively.

• All kind of Analysis of samples (Including Method Validation, process Validation, regular

Samples etc.)

• Maintaining the records related to Q.C. Dept.

• Involved in setup of QC lab.

• Worked with Sun Pharmaceutical Industries Ltd, (Jammu), as Q.C. Officer from June 08 to Oct 09.

• Routine analysis (Assay, Dissolution, Related substances, Content uniformity & physical

Parameters) for formulation development for Trial, Finish & Stability batches.

• Worked as Officer in ARD Lab, with Vitalife Laboratories Ltd,

(Gurgaon, Haryana) a US FDA Unit, Division of Arch Pharma (Mumbai) from Nov 09 to July10.

• Analytical method development and validation as per ICH guidelines by HPLC and UV

• Execution and interpretation of stability studies as per ICH guidelines.

• Preparation of Stability Protocols, Product Development Reports

and other relevant documents.

• Worked as Sr.Analyst with Karshini Pharmaceuticals Solutions, (Gurgaon) from July 10 to Aug 11.

•Routine analysis (Assay, Dissolution, Related substances) for formulation development

for Stability batches.

• Calibration of instruments like HPLC, UV, Dissolution Apparatus as per schedule

• Acquired good knowledge about troubleshooting and handling of many analytical and

Spectroscopic instruments e.g. HPLC, UV, FT-IR, Dissolution

• Data reviewing and report checking.

• Worked as Sr. Analyst with Arbro Pharmaceuticals Ltd. (New Delhi), from Sept 11 to June 12.

• Analytical method development and validation as per ICH

guidelines by HPLC and UV

• Documentation and compiling of results of the methods of

analysis as per GLP.

• Calibration of instruments like HPLC, UV, Dissolution Apparatus

Knowledge Base

LANGUAGES : C++, PERL, Visual Basic.

OPERATING SYSTEM : Windows 98 & XP..

DBMS : Sql, PL/Sql, Oracle 8.0, LIMS, Sample Manager

CASE TOOLS : MS - Word, Access, Power point.

Instrument knowledge

1 HPLC (Make Waters model 2695 with AUTO SAMPLER)

2 HPLC (Make AGILENT & SHIMADZU LC 2010CHT)

3 MELTING POINT APPARATUS

4 ABBES REFRACTOMETER

5 TABLET HARDNESS TESTER

6 FRIBRATOR TESTER

7 DISINTEGRATION TESTER

8 DISSOLUTION TESTER

9 pH METER

10 CONDUCTIVITY METER

11 BROOKEFIELD VISCOMETER

12 U-V SPECTROPHOTOMETER

13 FTIR

14 KFTITRATOR

References

1 Mr Yashpal Gautam

Management Staff, Cipla Sikkim; #090********

2 Mr. Manoj Singh (Executive)

Glenmark Pharma, Baddi; #720-***-****

3 Mr.Sagar Mehra, Manager ARD

Vitalife Laboratories, Gurgaon.

Personal Details

Father’s Name : Mr. F.D. Malik

Date of Birth : 24, August 1981.

Marital Status : Single

Languages Known : English, Hindi.

Current Salary : 6.8 lacs per annum

QAIS MALIK

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