Download 5713171075 Praveena EDUCATION Kingston University, London

[email protected],
5713171075
Praveena
EDUCATION
Kingston University,
London, UK.
Masters in Pharmaceutical Analysis.
09/2008-03/2010
P.R.R.M COLLEGE OF PHARMACY,
KADAPA, INDIA
Bachelor of Pharmacy
SKILLS
Software Skills
 R Statistical Software
 LIMS Database.
 Graph pad prism 5 & 6
 Noldus Etho-vision XT Software
 C programming language
 MS word, MS excel and MS PowerPoint
Analytical Techniques
 UPLC, HPLC
 GC
 UV Spectrometry
 Ion Chromatography
 Dissolution Apparatus
 Atomic absorption spectrometry
 Particle size analyzer
 KF
 Centrifuge
 Wet Chemistry
08/2004-06/2008
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Molecular Based Assays
Cell Culture Techniques
Cell-Based Assays
DNA sequencing
Recombinant DNA technology
Real time PCR
Bioprocess Techniques
 Cell Culture
 Biochemical and microbial analysis
 Centrifugation and Sterilization.
 Ion exchange Chromatography
 UV-spectrometry
 Knowledge of CDC and HHS
EXPERIENCE
Validation Analyst,
SCD Probiotics,
Kansas City.
Jun 2014-may 2016
Roles & Responsibilities:
 To ensure CGMPS are applied on Laboratory instruments.
 Executed validation activities and maintained laboratory.
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Maintained 21 CFR compliance of all laboratory instrumentation and related documents
Maintained protocols and technical reports.
Revised standard operating procedures.
Coordinated activities relating to the qualification, calibration and maintenance of
laboratory equipment.
Validated various instruments like HPLC, KF, UPLC.
Participated in laboratory investigations involving laboratory systems.
Provided training in calibration and troubleshooting instruments.
Research Associate,
RA Chem Pharma Ltd
Formulation R&D
Hyderabad, India.
Roles & Responsibilities:
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mar 2013 – mar 2014
Performed routine review of all documentation of manufacturing and processed batch
records.
Identified and developed solutions to assay-related problems.
Executed assay troubleshooting, optimization and validation experiments.
Prepared data tables, figures, project analysis plans and technical reports.
performed appropriate documentation to support testing procedures including data capture
forms, equipment logbooks, and inventory forms.
Identified and troubleshoot equipment problems.
Participated in company meetings and discussions.
performed overall operational planning and activities for the implementation and conduct
of studies (clinical trials, observational studies, compassionate use and registries) including
data management activities in compliance with GCP’s, SOPs and standards within
established timelines and budgets.
Procured lab supplies and reagents as needed.
Participated in method training and transfer to internal or external laboratories.
Engaged in review of investigations and validation of data.
Participated in new technology evaluations, transfer and implementation.
QC Analyst
Norbrook Laboratories,
(Vendor Maintenance Dept.,) Northern Ireland.
06/2011- 01/2013
Roles & Responsibilities:
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Investigated out of specification results and reporting to Manager.
Performed all the tests for the given samples according to the pharmacopoeias.
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Documented the process and procedures that was carried out throughout the experiment.
Prepared method verification protocols and Preparing work sheet excels for the projects
done.
performed all testing carried out in accordance to approved methods and in compliance
with GMP and GLP.
performed Method development and Validation of Raw materials.
Performed HPLC & GLC testing and method updates, assay Validation.
Prepared reports, data summaries, protocols, and batch records, and quantitative analysis
in accordance with current Good Manufacturing Practices (cGMP).
Involved in Verification of the calculations and reports.
Updated the log books, reviewing and confirming the test results.
Examined samples submitted by suppliers to obtain Vendor approval and maintaining a
catalogued store of retention samples representing each batch received.
Trained and directed technicians in performing their function within the laboratory with
particular reference to GMP and adherence to standard operating procedures.
Efficient in maintaining and preparing labs for FDA and MHRA audits.
Pharmacy Technician,
Leyton Orient Pharmacy, London.
Jan 2009 – Jun 2011
Roles and responsibilities:
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Supplied medicines to patients, on prescription and over the counter.
Assembled medicines for prescriptions.
Provided information to patients and other healthcare professionals.
Supervised pharmacy staff.
Answered patient questions and troubleshoot/resolve them promptly.
I have counselled patients on quit smoking programme and suggestions about disease
prevention.
Assisted patients with their drug therapy and pharmacy care issues.
Processed new and refill prescriptions.
Promoted patients’ drug compliance.
Reported all drug adverse events.
Establishing and maintaining good relationships with physicians and healthcare practices.
Assisted in streamlining communication with the patient, insurance companies,
pharmacist, nurses, lab and other healthcare-related parties.
Accepted the full responsibility for the patient’s pharmacy care plan.
Worked as part of a team to provide support to other members of the healthcare team.
KINGSTON UNIVERSITY, LONDON, UK.
09/2008-03/2010
Graduate Research Assistant and Teaching Assistant
 Calibrated and maintained weighing balances, KF and autotitrator.
 Validated HPLC.
 Performed thermo gravimetric analysis and differential scanning calorimetry on
polymers at various temperatures
 Worked on protein purification using Ion exchange and Size exclusion
chromatography.
 Teaching assistant and Lab coordinator for Pharmaceutical Analysis I.
 Involved in training the undergraduate students to handle and gets hands on experience
on the HPLC and also performing various Analytical techniques.
 Performing macro dissections and handling of laboratory animals.
 Master’s degree course work:
 Molecular and Atomic spectroscopy.
 Separation science.
 Pharmaceutical Analytical Technology.
 Statistics and Quality systems.
 RT-PCR.
 Advanced Statistical analysis.
Kingston Research Centre, London UK
01/2010-03/2010
Research Assistant
 Conducted Thermal Analysis of Car parts – Forensic Database using Differential
Scanning Calorimetry (DSC) and Thermogravimetric Analysis(TGA).
 Performed residual solvent analysis in various compounds using GC.
 Performed purity content of various raw materials using HPLC.
 Preparation of standard solutions, maintaining laboratory glassware, chemicals and
logbooks.
P.R.R.M COLLEGE OF PHARMACY,
KADAPA, INDIA
09/2004-08/2008
Undergrad Research Assistant
 Analyzed and determined the phytochemical profile and Analgesic studies of Pergularia
Daemia Leaves.
 The analgesic properties of these leaves were tested on the mice using the Eddy’s hot
plate method.
 Involved training the junior level undergraduate students in macro dissections of frog
and handling of mice and rabbits for various laboratory experiment purposes.
HETERO PHARMACEUTICAL LABS,
HYDERABAD, INDIA
06/2007-07/2007
Summer Intern
 Underwent Industrial training in the formulation of syrups, capsules, and tablets.
 Perform quality control tests for the formulate drugs and the proper packaging and
handling of drugs.
 Perform the qualitative and quantitative analysis of the products using the Shimadzu
HPLC system before releasing the batch into the market.
HONORS & Achievements
 Pharmaceutical Analysis Graduate Research, Teaching Assistantship and Summer
Research Grant.
 Method development of Norocalc bolus using Atomic absorption spectroscopy at
Norbrook.
 Performed method development of glucosamine Chondroitin sulphate using HPLC and
Autotitrator.
 Best poster presentation among the batch at Kingston University.