ASHW**********

Executive in Quality Assurance Department

  • India 
  • Graduation: Bachelor of Pharmacy Central India Institute of Pharmacy, Indore R.G.P.V Bhopal 2011.

  • Hourly / Daily / Monthly Rates: N/A

  • Languages: German(Native or Bilingual)

  • Last Update: 22.05.2019 at 05:45

Job Type
Full Time
Availability
Available
Country
India

Category :

Research & Development (R&D)

   

Keywords :

  

Director


Skills

Objective

To work sincerely and honestly to the best of my ability and potential with good academic credentials wish to contribute to the overall growth of the organization, in order to excel in profession.

Academic Qualification

Name of Examination and year

Institution

Board/University

Specialization

Marks (%)

Bachelor of Pharmacy 2011

Central India Institute of Pharmacy, Indore

R.G.P.V Bhopal

Bachelor of Pharmacy

72.3%

Senior Secondary Education, 2007

School for Excellence, Dewas (M.P)

M.P Board Bhopal

Biology

87.0%

Higher Secondary Education,2005

School for Excellence, Dewas (M.P)

M.P Board Bhopal

Science

83.0%

Work Experience

1.4 years working experience as an Executive in Quality Assurance Department in Alembic Pharmaceutical Limited, Panelav (Gujarat from Dec 2017 to present).

Handling of IPQA activities at shop floor.

Review of Batch Manufacturing Control Record and its compliance.

Calibration of IPQA equipment\\\'s.

Monitoring of Holding Time, Process Validation and Cleaning Validation at shop floor.

Review of Process related protocol and its report.

Periodic Performance Verification of Dynamic pass box.

Preparation and reviewof SOP\\\'s.

Review of Master Formula Record against MPC and MFC.

Involved in investigation related to deviations.

Review of Change Control related to process.

1.3 years worked experience as a Chemist in Quality Assurance Department in Ipca Laboratories limited (Jun 2016 to Nov 2017).

Handling of IPQA activities at shop floor.

Review of Batch Manufacturing Control Record and its compliance.

Monitoring of Holding Time, Process Validation and Cleaning Validation at shop floor against Sampling Plan.

Recording data in Annual product quality review.

2.2 years worked experience as a Supervisor in Quality Assurance Department in Sun Pharmaceutical Industries Limited (M.P)(Apr 2014 to Jun 2016).

Handling of IPQA activities at shop floor.

Review of Batch Manufacturing Control record and its compliance.

To check if any irregularities found then inform to concern personal to take corrective action, and intimate to higher authority.

Prepare Holding Time Study Protocol.

Knowledge of all online SAP system activities Like Sampling, COA check

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