Chemist

Career Overview

Enthusiastic Chemist with proven expertise in pharmaceutical industry, accomplished at testing new drugs and analysis of exiting formulas well as finished products, stability, IPC, API testing using HPLC, GC,UPLC and various physical and chemical methods. Focused Chemist who is highly effective in using USP, EP, BP methods, in-house methods, GMP and GLP and ALCHOA -plus practices. Motivated Chemists seeking lasting career in the pharmaceutical industry or biotech and related industry.

Areas of Expertise

Physical and Chemical Testing

HPLC, GC, UPLC

Spectrophotometer

Thin-Layer Chromatography

FTIR

Karl-Fisher

GMP /GLP

LabWare LIMS /Empower

pH meter, balances

Viscometer /Osmolarity

Hunter color (easy match)

Microsoft word, Excel, PowerPoint

Quickly adapt to new software

Particle size image analysis (Northern Eclipse)

In vitro analysis

TGA/DSC

Professional Experiences

QC Chemist

Europhin Alphora Research 2017-2020

Perform routine lab testing procedure for IPC, operate analytical instruments (including but not limited to GC, UPLC, HPLC, FTIR, KF)

Assume role of Shift leader and responsibility in his /her absence

Review and approve test result for IPC, API, Review documentation for accuracy

Communicate review outcome to other chemist for correction and continuous improvement.

Provided technical support to other chemist for larger projects and tighter deadlines, to ensure timely completion of projects. Communicate results/reports to management

R and D Chemist

Taro Pharmacuticals,Toronto 2015-2016

Tested various products on R&D stability.

Compiled all data obtained from testing and observations and completed report summaries for submission.

Recognized OOS or OOT results and under the direction of the Supervisor assisted in the completion of lab investigations.

Performed additional related duties, as assigned, in accordance with job responsibilities and necessary departmental objectives, optimizing work flow to meet business requirements and achieving corporate goal.

Chemist

Estee Lauder Cosmetics,Toronto 2014-2015

Conducted in process test for mass cosmetic such as drop point, viscosity, specific gravity, break point for lipsticks

Performed analytical testing for sunscreen in cream preparations

Analyzed Cosmetic Samples for OTC and preservatives

Performed analysis to ensure quality control of raw materials such as pH, Viscosity, IR, LOD, Acid Value, Saponification Value, bulk density, color test and melting point

Responsible for Process troubleshooting and out of specification results

Performed raw material test utilizing wet chemistry and HPLC (purity, potency, Id) as per established methods or

QC Chemist

Apotex Inc, Toronto Canada 2007- 2014

Performed routine analysis of various pharmaceutical dosage forms and Stability testing using analytical instruments to release product on time

Skilled in testing particle size, particulate matter and image analysis of otic, ophthalmic, nasal and oral solutions and suspensions.

Liaised with various groups, teams to complete validation testing to launch first to market products.

Skilled in STR testing to close complaints, worked towards resolutions of the issues.

Ensured all results are within established specifications /procedure to meet FDA and health Canada guideline

Adhered to all SOP (Standard Operation Procedure), GLP (Good Laboratory Practices) and GDP (Good Documentation Practices) to meet all compliance and regulatory requirements.

Met quality and turnaround time specifications required by internal and external clients.

Maintained a high level of work production in fast paced lab environment with minimal supervision by optimizing workflow to meet business requirements.

Acquired fast learning ability and adaptability to new procedures and processes.

Performed daily calibration of laboratory equipment such as balances, pH meters, Milli Q water according to established calibration program and GMP requirements.

Worked collaboratively in cross functional tea

Document Reviewer

Quality Compliance Laboratories, Markham Canada 2006 – 2007

Conducted routine analysis of various pharmaceutical products/reviewed test work sheets / ensured all tests performed according to required procedures/results are within established specifications

Assisted in data review, ensured all corrections are made in appropriate manner, meeting deadlines.

Maintained and updated daily C of A data base for internal and external customers.

Prepared SOP, Deviation reports,OOS investigation report, Change control report Batch Records to maintain compliance

Conducted test and analysis of raw materials and finished drug product, to increase efficiency across team

Liaised with various departments to co-ordinate testing and improving efficiency

Technical Team Member

GlaxoSmithKline, Mississauga Canada 2003- 2005

Demonstrated knowledge of Production process and Equipment

Performed packaging with precision in GMP environment following SOP document guidelines and EHS Regulations/Assisted in production process by completing tasks for IMS.

Experienced in verifying correctness of packaging, materials and bulk product leading to right first time.

Executed tasks in primary, secondary and specialty packing.

Demonstrated strong working knowledge of inspection of labeling, lot number, batch number, expire date, line sorting, logging and finished pack /Assisted in sampling and visual factory improving visibility of process for all clients.

Education

Diploma QC testing

Academy of Applied Pharmaceutical Sciences

Diploma in Pharmaceutical Quality Control

Degrees

Quaid- I -Azam University, Islamabad Pakistan

M.Sc., M.Phil. Biological Sciences

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