analytical chemist resume example with 20+ years of experience

Jessica Claire
, , 100 Montgomery St. 10th Floor (555) 432-1000,

Enthusiastic Analytical Chemist eager to pursue a lasting career in the pharmaceutical industry.

  • Advanced chemical research.
  • Knowledgeable in gravimetric determination,FTIR,UV-VIS spectroscopy.
  • Karl Fischer water determination.
  • Experienced in Analytical Method Evaluation,Method Development and Method Validation.
  • Knowledgeable in GC,HPLC,UPLC,TLC chromatographic instrumentation.
  • Particle size analysis.
  • Polarimeters.
  • Titration.
  • Heavy metal analysis
  • Specific gravity.
  • GLP environment.
  • Safety Control Committee Member.
  • Lab maintenance expert.
  • Laboratory instrument troubleshooting and maintenance skills.
Expected in to to Master of Science | Computer Management Pune University, Pune, Maharastra GPA:


Expected in to to Bachelor of Science | Industrial Chemistry-Vocational Sardar Claire university, V.V Nagar, Gujarat GPA:


Expected in to to Master of Science | Management Information System Holy Family University, Philadelphia, PA GPA:



Quickly developed and validated three pharmaceutical detergent-cleaning validation method for FDA response during annual FDA inspection in march 2012.

08/2006 to Current Analytical Chemist Asahi Kasei America | Fowlerville, MI,
  • Performing qualitative and quantitative analysis of raw material, finished product, stability, process validation,and cleaning validation sample-using analytical instrumentation such as GC, UPLC, HPLC, TLC, UV/VIS Spectroscopy, pH metry analysis, particle size analysis, Karl Fischer, FTIR, wet chemistry, etc.
  • Performing the analytical method evaluation, method development, method validation(Linearity, Recovery, Specificity, LOD, LOQ, Forced degradation, Precision, etc.) and method transfer of excipient, raw material, finished product, cleaning agent and cleaning validation of carryover from previously run product on pharmaceutical equipment.
  • Experienced in method validation protocol writing, method validation report writing, method transfer protocol writing, method transfer report writing, and analytical method writing.
  • Writer, publisher and reviewer of pharma ready system.
  • Have in depth knowledge of chromatographic analysis such as tailing factor, resolution, peak purity, purity angle, purity threshold, capacity factor, theoretical plate count etc. of chromatographic peak. As a professional chromatographer, troubleshoots the instrumentation, method development challenges and routine LIR investigations.
  • Auditing/Reviewing the routine analytical work such as QC release, stability testing, method validation, cleaning validation performed by other analyst.(peer review)
  • Maintaining all training and trainer record using compliance wire learning management system.
  • Having fundamental understanding of GxP, ICH guideline, cGMP’s/GLP’s and USP/NF compendial monograph.
  • Serving on a laboratory committee such as safety, suggestion, cGMP, SOP and news latter.
  • Maintaining laboratory notebook as per the FDA regulation and cGMP requirement.
  • Performing other duties as assigned such as product technical package and specification evaluation.
01/2004 to 08/2006 QC-Chemist Ppg Industries, Inc. | Eugene, OR,
  • Performed finished product and stability sample testing using HPLC, UV/VIS spectrophotometric analysis.
  • Performed blend uniformity, assay, content uniformity, residual solvents, dissolution, TLC, IR, and water determination of finished product and stability samples.
  • Performed all job responsibilities in safe and efficient manner.
  • Released product before dead line.
  • Trained other personnel in analytical instrumentation, test methodology and auditing the analytical work.
  • Performed LIR investigation as needed. Followed corrective action and preventing action to eliminate the cause of non-conformities.
04/2003 to 01/2004 Tableting Operator Splendid Spoon | New York, NY,
  • I have operation experience of tablet press such as Kilian TX, Synthesis 500/600, FETTE, RTS machines.
  • Performed the tasks as per the batch record.
  • Material handling, inventory upgradation and safety precaution were carried out during the tablet press operation.
06/2002 to 02/2003 Software Developer Cyber Software Solutions | City, STATE,
  • The existing systems were evaluated.
  • Deficiencies were identified by interviewing users of the system, consultants and support personal.
  • The new system requirements were defined with specific proposals for improvement.
  • The new systems were developed with respect to physical construction, hardware, operating systems, programming, communications and security issues. The new components and programs were installed.
  • The users of the system were trained in its use. Maintenance kept up all times.
  • Users of the system kept up to date concerning the latest modifications and procedures.
Additional Information

Academic Project:

Processing and refining crude oil- at Gas Authority of India:

  • Evaluated the performance of the fully automated plant consisting of distillation, cracking, treatment, and reforming-processes.
  • Optimized the Liquefied natural gas process at minus 160 degree centigrade.

Database Design- at SIOM college:

  • Designed library database management software using oracle.


  • Software: Microsoft word, Excel, PowerPoint, Empower, Chemstation.
  • Programming Languages: Visual Basis, UNIX, C, C++, Data structure using C.
  • Operating Systems: Windows 98/NT, UNIX, Macintosh, Windows XP, Vista.


  • Phenomenex- HPLC Method Development Certification, ChromSource-Gas Chromatography Certification, Waters: Apex Track Integration Certification.

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Resume Overview

School Attended

  • Pune University
  • Sardar Claire university
  • Holy Family University

Job Titles Held:

  • Analytical Chemist
  • QC-Chemist
  • Tableting Operator
  • Software Developer


  • Master of Science
  • Bachelor of Science
  • Master of Science

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