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Email: jobs@plastemart.com, hr@plastemart.com

Download Date: 2/6/2025 5:27:30 AM

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RefNo: CA - 11293
Gender: Male
Age: 43

Designation: Senior Executive

Highest Education Level: Masters - Degree

Current Gross Salary: 250000 250000 /Annum 

Expected Gross Salary: 300000 300000 /Annum 

Preferred Location: Maharashtra

Notice Period: 30 Days

Education Details: 
Master of Science (Organic Chemistry) from S.R.T.M.U. Nanded, with First Class in 2007



Skill Sets: 
Computer Skills: Completed course in Web technology curriculum (WTC) and adept at MS Office 

Work Experience: 17.1

Work Experience Details: 
Q.A. Officer

Since April 2011 

Company Profile: Manufacturer and Exporter of Packaging and Containers.  

Job Profile:

Documentation in quality assurance (QMS)

Make SOPs as per pharma guidelines.

Make COA, specification report. 

To work all related to IPQA and Q.A. documentation.

Worked on CAPA.

Knowledge of change control, qualification.

To follow the guideline as ISO 9001-2008 industry.   



Q.C. Officer

From Apr 2010 to Feb 2011

Company Profile: Leading Formulation Drug Industry.

Job Profile:

Stability section. Performing stability study like

Photo stability 

Thermal cycling study

Temperature Excursion study.

Kept batches for a stability studies as per ICH guideline

Maintain stability sample pull-out log, Equip.log, etc.                   

Prepare protocol and trend chart, STF, of new drug product.To                   

Perform analysis of stability study sample and inprocess   

Product as per specification.

Analysis and reporting of stability sample

Report any deviations, non-conformities, out of specifications results and arising out of any of the activities performed to manager Q.C                                                

Finished product section 

Analysis and Reporting of Finished Products (Tablet, Capsule, Injection etc)

Report any deviations, non-conformities, out of specifications results arising out of any of the activities performed to manager Q.C   

Validation 

Cleaning validation

Analysis and Reporting of Cleaning validation sample.

Report any deviations, non-conformities, results arising out of any of the activities performed to manager Q.C

Process validation

Analysis and Reporting of Process validation sample.

Report any deviations, non-conformities, results arising out of any of the activities performed to manager Q.C



Q.C. Chemist

From Sept 2009 ? Apr 2010

Midas-Care Pharmaceutical Pvt Ltd

Job Profile:

Deft at analysis of bulk product, water by K.F. Assay by titration method and standardization for normality 

Involved in Patent search and literature search. Dexterous at formulating drug designs & strategies to meet deadlines & ensured quality.

Adhering to the various quality measures, SOP and functioning as an instrumental member for designing and implementing procedures, control systems to maintain quality standards

Establish and use service level and response time objectives while planning and managing the service-level quality using real-time management skills. 

Conducted & analyzed preformulation and compatibility studies.

Strict adherence to statutory compliances & obligations. Pivotal in formulating protocols and ensuring the ICH guidelines are followed

Process optimization & Scale-up trials. Accountable for executing & trouble shooting exhibit batches

Prepared master formula record and technology transfers documents, preparation of development reports as per the regulatory norms for different products.

Troubleshoot any issues occurred during product development. Assisted product validation & revalidation.

Provided required technical documents to the regulatory department.



R & D Chemist

From Aug 2007 ? Aug 2009

Pharmaffiliates Analytics & Synthetics Pvt Ltd.

Job Profile:

Job responsibilities include Synthesis of API, Intermediates and drugs Impurity 

Tramadol hydrochloride, Synthesis of Fusidic Acid Impurities, 6-Methoxy-2-napthaldehyde, Iopamadol, Iohexol.

Monitored the reactions, Synthesizing of intermediates, Apis, and drugs impurities by using varies parameters such as Temperature, PH adjustment and TLC checking.

Used solvents, reagents & catalysts in synthesis reaction as well as hands on experience in distillation 

Conversant with Oxidation, reduction, nitration, sulphonation, and dehydration as well as performed Halogenations and dehalogenation reactions.

Used column chromatography system for purification and mixture separation. 

Future Goals: 
To be a Well Experienced in Quality Field of the Industry






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