Analytical Scientist

• Sep 2019 - Present

Method Development, Validation, Regulatory Compliance Method Development, Validation, Regulatory Compliance

OTC Manager

• Jun 2019 - Present

Pharmacy technical assistant

• Aug 2017 - Present

• Maximizing department sales and profit with direction from the Pharmacy Manager.• Maintaining patient confidentiality and follow all practices consistent with the Privacy Act.• Practicing the 3 Meter Attitude. Answering Customer calls promptly.• Maintaining 100% in stock always. Prepare blister pack.• Rotating stock and checking for expired products.• Ensuring the merchandise is properly signed and priced.• Maintaining modular labels. Additional Responsibilities• Adheres to all company policies and standard operating procedures

Senior Research Associate Analytical-II

• Feb 2015 - May 2017

Operate HPLC, PREP HPLC, LCMSMS, LCMS, and NMR.DATA INTERPRETATION OF NOVEL COMPOUNDMETHOD DEVELOPMENT IN HPLC, LCMS.Participate in a recruitment process.• Analytical method development for many complex molecules by conducting different experiments andtests using analytical instruments such as HPLC/LC-MS /PREP HPLC/ GC.• Conduct Project/sample analysis using developed and validated methods.• Troubleshooting for problematic analytical issues (low sensitivity, ion suppression, poorchromatography, less reproducibility, etc.)• Perform literature searches for different compound and substances; know the chemical composition,natural properties and reactivity of the compound to develop a method of the compound/substanceusing analytical instruments.• Train the analytical staff for analytical SOPs and other relevant Instrumental Practical trainings.• Maintain the schedule for internal and external calibration of the analytical instruments.• Participation during Installation and preventive maintenance of different analytical instruments.• To ensure that Analytical Research and Development lab is being maintained properly and all theequipment’s/instruments assigned, are kept clean and maintained.• Preparing and Checking the Analytical sections of Final Report.

Research Associate

• Feb 2013 - Feb 2015

• Develop and validate bio-analytical method in biological matrix.• Analyze biological samples of allotted projects.• Handling and operation of LCMSMS.• Calibration of PH meter, Analytical and Micro balance in bio-analytical department.• Prepare and review of Draft SOPs and Method SOPs.• Ensure effective implementation of GLP and 21CFR by checking instrument label, completion of logbook of equipment and instruments and ensuring the instrument calibrations are done before date.• Reporting about status of an ongoing projects and method validation to group leader.• To communicate about the performance of lab equipment and status of resource availability to the groupleader.• To resolve the system, projects and method validation QC/QA findings.• Transfer of concentration table of subject sample for Pharmacokinetic analysis