Hinal Patel

Address : ***** ******* ** *

robinsonville,

MS38664.

Cell No : 937-***-****

Email Id : ac96ah@r.postjobfree.com

Objective:

To work hard with full dedication for the achievement of organization objective under satisfying job contact, hence enhancing my skill and knowledge and ready to learn new thing.

Education:

Master of Pharmacy Major in Quality Assurance 2016 (Equivalent to MS as per WES)

Bachelor of Pharmacy 2013 (Equivalent to BS as per WES)

Skill:

Highly responsible and superb multitasker, able to handle multiple projects efficiently and accurately. Effective independent work as well as excellent coordinator with other members of the team. High skill in maintaining professional relationship with all level of staff. Outstanding analytical and problem solving ability.

Work experience:

Furthermore, I have working experience in Ipca laboratories with Quality Control and Research and development department from May 2015 to April 2018

Perform maintenance on complex laboratory equipment including HPLC and GC systems.

Experience with instruments like GC, HPLC, IR, Auto-titrator, Kal-fiesher, pH meter, viscometer, and colorimeter.

Calibrated and verified instruments in accordance to daily, monthly, and quarterly maintenance schedules.

Initiated change control to method and procedures requiring modification.

Prepared SOPs (Standard Operating Procedures) and the ongoing maintenance of process and procedure documentation.

Selected by upper management to join task force which developed and delivered documentation and training for in-house applications.

Knowledge of FDA regulations, cGMPs, GLPs, SOPs, ICH guideline, CAPA's, internal and external audit.

Interpreted pharmacopoeia guidelines to perform testing of raw materials, in-process materials, and finished pharmaceutical products.

I have working experience with Quality assurance in Zydus Cadila healthcare from September 2013 to October 2014.

Monitoring manufacturing activity and all GMP documentation for compliance.

Issuance and reviewing of Batch manufacturing record for reconciliation and completeness.

Preparing QC/QA documents.

Maintaining the matrix of all controlled documents.

Coordinate activities with R&D and manufacturing department

Preparing of annual product review report and quality overall summary reports.

Review and revision of QA department SOPs and associated forms.

Work as a Trainee at Food & Drug Laboratory.

June 2012 – August 2012

Worked in various departments undergoing intensive laboratory Training as a Pharmacy student.

Pharmacognosy: Worked on TLC and HPTLC of the drug.

Pharmacology: Experimented on mice and rabbits on Pyrogen test and LAL test.

Pharmaceutical Chemistry: Assay of various marketed drugs.

Microbiological: Pyrogen tests on water sample and baby powder.

Research Work:

-Analytical method Development and validation for Related substance of Hydralazine Hydrochloride by the HPLC (Impurity Profiling).

-Development and validation of analytical method for simultaneous estimation of Diclofenac sodium and Tramadol hydrochloride in pharmaceutical formulation

Declaration:

I hereby declare that the above written particulars are true to the best of my knowledge.

Hinal Patel.

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