Buu Tu resume
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Buu Tu is seeking a position in R&D laboratory in the pharmaceutical industry where he can apply his skills in product formulation. He has a Master's degree in Industrial Pharmacy and Bachelor's degree in Pharmaceutical Sciences. His past experience includes working as a laboratory technician at Colorcon Inc. where he assisted in formulating immediate release tablets. He also has experience guiding organic chemistry lab students and conducting research evaluating properties of OTC medications and developing generic formulations. He is proficient in various analytical techniques and instrumentation relevant to pharmaceutical product development.
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Buu tu resume
Buu Tu is seeking a position in R&D laboratory in the pharmaceutical industry where he can apply his skills in product formulation. He has a Master's degree in Industrial Pharmacy and Bachelor's degree in Pharmaceutical Sciences. His past experience includes working as a laboratory technician at Colorcon Inc. where he assisted in formulating immediate release tablets and followed research plans to increase productivity. He also has teaching experience as an organic chemistry lab teaching assistant and coursework experience in analytical techniques and cell culture.
Buu Tu resume
Buu Tu is seeking a position in R&D pharmaceutical laboratory applying his skills in product formulation. He has a Master's degree in Industrial Pharmacy from St. Johns University and a Bachelor's degree in Pharmaceutical Sciences from USP. His experience includes laboratory work at Colorcon developing generic immediate release tablets and research projects developing formulations at St. Johns and USP. He is proficient in analytical techniques and instrumentation relevant to product development.
Cadth 2015 e4 adaptive design april 2015 final lourenco
Health Canada regulates clinical trials and drug approvals. Adaptive clinical trial designs are increasing and can modify aspects of ongoing trials using accumulating data. Health Canada's main concerns are appropriate scientific questions, error control, and avoiding bias. Examples seen include adaptive randomization, sample size changes, and seamless phase 2/3 designs. Case studies demonstrate increased complexity, new statistical methods, and more simulation use. Health Canada recommends early consultation and education on adaptive designs.
Cadth 2015 e4 lourenco adaptive design april 2015 final
Health Canada regulates clinical trials and drug approvals. Adaptive clinical trial designs are increasing and can modify aspects of ongoing trials using accumulating data. Health Canada's main concerns are appropriate scientific questions, error control, and avoiding bias. Examples seen include adaptive randomization, sample size changes, and seamless phase 2/3 designs. Case studies demonstrate increased complexity, new statistical methods, and more simulation use. Health Canada recommends early consultation and education on adaptive designs.
Significance of BA/BE studies in drug research and evaluation of different as...
PharmaCon2007 Congress, Dubrovnik, Croatia "New Technologies and Trends in Pharmacy, Pharmaceutical Industry and Education" http://www.pharmacon2007.com
Abstract is available at http://www.pharmaconnectme.com
Clinical studies and trials on traditional medicine and natural products
Clinical studies and trials on traditional medicine and natural productsProf. Dr. Basavaraj Nanjwade
This document discusses clinical studies and trials for traditional medicines and natural products. It provides an overview of the different phases of clinical drug development, including Phase I trials which test safety in small groups, Phase II trials which assess efficacy and side effects in larger patient groups, and Phase III trials which demonstrate safety and efficacy in large patient populations. The goal of clinical trials is to determine appropriate dosages and identify potential risks before drugs can be approved for medical use.Clinical drug design
The document discusses the process of clinical drug design and development. It begins by defining drugs and their targets in the body. It then outlines the various phases of clinical trials that drugs must undergo to test their safety and efficacy before regulatory approval. These phases progress from small healthy volunteer groups to large patient populations. The document also discusses approaches to drug design like computer-aided design and targeting specific sites in the body. Quality by design principles are highlighted as important to developing products that meet clinical needs. In total, the clinical drug design process involves methodical testing from early targets to final approved treatments.
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The document discusses Quality by Design (QbD) principles for pharmaceutical product development. It defines key QbD concepts like quality target product profile, critical quality attributes, critical material attributes, critical process parameters, risk assessment, design space, and control strategy. It provides examples of applying these concepts for developing different dosage forms like tablets, capsules, solutions, and creams. The document aims to guide systematic development of pharmaceutical products using a QbD approach with a focus on understanding and controlling critical factors influencing quality.
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Buu tu resume
Buu Tu is seeking a position in R&D laboratory in the pharmaceutical industry where he can apply his skills in product formulation. He has a Master's degree in Industrial Pharmacy and Bachelor's degree in Pharmaceutical Sciences. His past experience includes working as a laboratory technician at Colorcon Inc. where he assisted in formulating immediate release tablets and followed research plans to increase productivity. He also has teaching experience as an organic chemistry lab teaching assistant and coursework experience in analytical techniques and cell culture.
Buu Tu resume
Buu Tu is seeking a position in R&D pharmaceutical laboratory applying his skills in product formulation. He has a Master's degree in Industrial Pharmacy from St. Johns University and a Bachelor's degree in Pharmaceutical Sciences from USP. His experience includes laboratory work at Colorcon developing generic immediate release tablets and research projects developing formulations at St. Johns and USP. He is proficient in analytical techniques and instrumentation relevant to product development.
Cadth 2015 e4 adaptive design april 2015 final lourenco
Health Canada regulates clinical trials and drug approvals. Adaptive clinical trial designs are increasing and can modify aspects of ongoing trials using accumulating data. Health Canada's main concerns are appropriate scientific questions, error control, and avoiding bias. Examples seen include adaptive randomization, sample size changes, and seamless phase 2/3 designs. Case studies demonstrate increased complexity, new statistical methods, and more simulation use. Health Canada recommends early consultation and education on adaptive designs.
Cadth 2015 e4 lourenco adaptive design april 2015 final
Health Canada regulates clinical trials and drug approvals. Adaptive clinical trial designs are increasing and can modify aspects of ongoing trials using accumulating data. Health Canada's main concerns are appropriate scientific questions, error control, and avoiding bias. Examples seen include adaptive randomization, sample size changes, and seamless phase 2/3 designs. Case studies demonstrate increased complexity, new statistical methods, and more simulation use. Health Canada recommends early consultation and education on adaptive designs.
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This document discusses clinical studies and trials for traditional medicines and natural products. It provides an overview of the different phases of clinical drug development, including Phase I trials which test safety in small groups, Phase II trials which assess efficacy and side effects in larger patient groups, and Phase III trials which demonstrate safety and efficacy in large patient populations. The goal of clinical trials is to determine appropriate dosages and identify potential risks before drugs can be approved for medical use.Clinical drug design
The document discusses the process of clinical drug design and development. It begins by defining drugs and their targets in the body. It then outlines the various phases of clinical trials that drugs must undergo to test their safety and efficacy before regulatory approval. These phases progress from small healthy volunteer groups to large patient populations. The document also discusses approaches to drug design like computer-aided design and targeting specific sites in the body. Quality by design principles are highlighted as important to developing products that meet clinical needs. In total, the clinical drug design process involves methodical testing from early targets to final approved treatments.
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The document discusses Quality by Design (QbD) principles for pharmaceutical product development. It defines key QbD concepts like quality target product profile, critical quality attributes, critical material attributes, critical process parameters, risk assessment, design space, and control strategy. It provides examples of applying these concepts for developing different dosage forms like tablets, capsules, solutions, and creams. The document aims to guide systematic development of pharmaceutical products using a QbD approach with a focus on understanding and controlling critical factors influencing quality.
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This document discusses the scope of pharmacy and clinical research. It begins by introducing various topics related to pharmaceutical sciences including pharmacy, pharmaceutical formulation, the pharma industry, and the scope of pharmacy. It then defines clinical research as the systematic study of safety and efficacy of new pharmaceutical products in humans. The document goes on to explain the different phases of clinical trials, from preclinical research through phases 0-IV. It emphasizes the importance of research for developing new diagnostic tests, drugs, surgical techniques, and combination treatments. Finally, it briefly mentions some job opportunities in clinical research.
Bioequivalence studies
The document discusses bioequivalence studies, which are conducted to demonstrate that a generic drug is equivalent to an innovator drug. It covers the objectives of bioequivalence studies, the phases including clinical, bioanalytical and pharmacokinetic evaluation. The phases involve protocol preparation, ethics approval, subject selection, sample collection and analysis. The document also discusses various parameters of bioanalytical method validation including selectivity, accuracy, precision and stability. Regulatory requirements for bioequivalence studies from agencies like FDA and EMEA are also mentioned.
The cell line integrity
1) Cell lines used for manufacturing biopharmaceuticals must meet strict quality criteria to ensure high quality, stable production. This includes being capable of high productivity, producing molecules with the appropriate structure and quality, and accepting and stably expressing foreign DNA.
2) Master cell banks are critical starting materials that are extensively tested for sterility, mycoplasma, and adventitious agents to ensure safety.
3) Routine monitoring of cell line integrity and performance during biomanufacturing helps evaluate the process and cell line stability over time.
Allergan Fellowship Report 2012-2013
This document summarizes the Gavin Herbert & USC Vision clinical scientist fellowship program between Allergan and USC School of Pharmacy established in 1977. The fellowship aims to train pharmacists to be experts in both clinical practice with patients and physicians as well as research in the laboratory. Fellows gain drug development and commercialization experience at Allergan while also participating in academic activities at USC such as precepting students, guest lecturing, and attending regulatory science courses. The program has a 100% success rate of fellows obtaining jobs in pharmaceutical industry roles such as regulatory affairs, clinical development, medical affairs, and more.
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- My session at the third international educational fair in Egypt (Edu link fair 2017).
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RAJENDRA_CV
Rajendra Balaso Kolape has over 13 years of experience in quality control and analytical development with companies like Johnson & Johnson, Ranbaxy Labs Ltd., and Cipla focusing on raw material analysis, stability testing, method development and validation, instrument qualification, and audit management. He currently holds the role of Group Leader - Clinical Release & Stability at Janssen and has a Master's degree in Chemistry, with a goal of excelling in analytical and related research to ensure business success and patient safety.
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Good Laboratory Practice (GLP) is a quality system for conducting safety testing of products like pharmaceuticals, pesticides, and chemicals. It aims to develop quality test data, ensure mutual acceptance of data between countries, and protect human health and the environment. GLP provides principles for test facility organization and management, quality assurance programs, facilities, equipment, study conduct, recordkeeping, and reporting to ensure safety studies are properly planned, performed, monitored, and documented. Key parties involved include test facility management, study directors, quality assurance personnel, and study staff.
Drug Formulations
The document discusses the importance of drug formulation in pharmaceutical development. It states that drug formulation involves combining active drugs with other substances to create safe and effective products for human consumption. However, formulation is often overlooked in early drug development stages. This can lead to costly delays if not addressed. The document recommends adopting an integrated approach where formulation is considered throughout development. Formulations should be tailored to each study phase and developed with a comprehensive understanding of the drug's properties. With open communication across teams and formulation as an integral part of development, companies can reduce risks and costs and get products to patients more efficiently.
Equivalence approches for complex generics DIA 11 april 2019
This document discusses approaches for demonstrating bioequivalence of complex generic drug products. It begins with an overview of the pre-ANDA program for complex generics, including product development meetings, pre-submission meetings, and mid-review cycle meetings. It then discusses specific challenges and considerations for complex active ingredients like peptides, as well as example complex drug products like sevelamer carbonate tablets and ophthalmic ointments and suspensions. The document emphasizes that demonstration of bioequivalence for complex generics often requires alternative approaches like in vitro studies and physiochemical characterization due to challenges with clinical endpoint studies.
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Suzanne N. Tineo is an experienced medical lab technologist with 15 years of experience at Labcorp and Duke Hospital seeking a position in the Triad area of North Carolina. She has excellent clinical laboratory skills in conducting and analyzing assays and resolving complex problems. She is accurate, reliable, diligent and focused on completing all lab procedures in a timely manner while working well under pressure. She has a bachelor's degree in biology and certifications in BLS, CPR and First Aid.
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The cell line integrity
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2) Master cell banks are critical starting materials that are extensively tested for sterility, mycoplasma, and adventitious agents to ensure safety.
3) Routine monitoring of cell line integrity and performance during biomanufacturing helps evaluate the process and cell line stability over time.
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This document summarizes the Gavin Herbert & USC Vision clinical scientist fellowship program between Allergan and USC School of Pharmacy established in 1977. The fellowship aims to train pharmacists to be experts in both clinical practice with patients and physicians as well as research in the laboratory. Fellows gain drug development and commercialization experience at Allergan while also participating in academic activities at USC such as precepting students, guest lecturing, and attending regulatory science courses. The program has a 100% success rate of fellows obtaining jobs in pharmaceutical industry roles such as regulatory affairs, clinical development, medical affairs, and more.
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This document discusses the opportunities and future for pharmacists. It begins by explaining that pharmacy is an attractive career option that provides many job opportunities due to advances in technology and the pharmaceutical industry. It then outlines various job roles for pharmacists in industries, hospitals, retail, academics, and research. It also describes the skills and qualifications needed for different pharmacy careers including diploma, bachelor's, Pharm.D, master's and doctorate degrees. Overall, the document presents the wide range of career paths available to pharmacists across different settings.
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Protocol
This document outlines the key components and contents of a research protocol. It explains that a protocol describes the objectives, methodology, and organization of a clinical research study. It provides details on the various sections that should be included in a protocol such as background information, trial objectives, design, selection and withdrawal of subjects, assessment of efficacy and safety, statistics, ethics, data handling, and publication policy. The protocol acts as a guideline for researchers and includes important details about the study such as the investigational product, dose, subject inclusion/exclusion criteria, study duration, and statistical analysis plan. Developing a standardized protocol is important to clarify the research questions and ensure proper planning and conduct of the clinical trial.
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Journal of Bioequivalence Studies (JBS) is an open access, peer reviewed journal that publishes the most relevant and reliable researches with respect to the subject of Bioequivalence studies which includes pharmacokinetic and pharmcodynamic properties of a drug. JBS publishes original articles, review articles, case reports, short communications, etc.
Clinical trials
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- Objective of seeking a role where he can utilize his skills and experience to help ensure an organization's compliance with regulatory standards and quality management systems
OscarLara_resume_2015current
Oscar Lara has over 12 years of experience in pharmaceutical research and development, holding positions at companies such as Regeneron Pharmaceuticals, Ortho-Clinical Diagnostics, and Hoffmann-La Roche where he conducted assays, managed projects, trained staff, and ensured compliance with regulations. He holds a Master's and Bachelor's degree in Biology from Fairleigh Dickinson University and has skills in areas such as ELISA, cell culture, data analysis, and laboratory software.
Martha ariza resume
Martha Ariza Sáenz is a biologist with a PhD in Pharmacy who has worked for 8 years in Spanish research institutions. She has experience with analytical techniques such as HPLC, FTIR, UV-Vis, DSC, AFM and SEM, as well as cell culture, in vitro release techniques, fluorescence probe marking and peptide synthesis. Her career includes roles as a predoctoral researcher, senior technician, and QA technician. She has published research on topics including nanoparticle-based HIV treatment and the use of polyphenols for conditions like polycythemia vera.
Sarah's resume 12.22.15
Focused Chemical/Microbiological technician highly effective at following USP methods and GMP practices with pharmaceutical and medical device experience.
Chemist accomplished in GC, HPLC, analytical and assay methods used on raw material and finished products to assure the quality and purity of products. Certified in Clinical Trials and Drug Development and worked side by side a chemical formulator R&D chemist for 3 years. Coordinated process validation procedures, stability program, chemical waste management system, calibration program, laboratory set up, ordering and SOP procedural writing.
Versed Microbiological surface and air quality testing, process validation, microbiological identification, trending, tracking, gram staining techniques and microbiological morphology. Certified in Pharmaceutical Microbiology.
CPHendrix Resume 6-13-15
Charlene P. Hendrix is seeking a laboratory position where she can utilize her experience in analytical chemistry and microbiology. She has over 25 years of experience performing quality control analysis on food, water, environmental, and medical samples. Her experience includes writing and revising standard operating procedures, supervising laboratory personnel, and ensuring compliance with FDA and USDA regulations. She has a Bachelor's degree in Chemistry and an Associate's degree in Medical Laboratory Technology.
GLP.pptx
This document provides an overview of Good Laboratory Practices (GLP). It discusses that GLP is an FDA regulation that provides a framework for planning, conducting, monitoring, recording, and reporting nonclinical laboratory studies. The document outlines the history of GLP and why it was created, describes key aspects of GLP such as organization, personnel, facilities, equipment, test systems, and record keeping. It also discusses objectives of GLP and highlights an important example of a lab that was found to be fraudulent and engaged in poor practices.
RESUME
Ch.Rangaih is seeking a position in an organization with strong vision and mission to enhance growth and development. He has a M.Pharmacy from JSS College of Pharmacy with 79.64% and a B.Pharmacy from Nalanda College of Pharmacy with 76.05%. He has over 2 years of work experience as an Assistant Quality Control Officer and Junior Quality Control Chemist. He is proficient in instrumentation skills like HPLC, UV spectroscopy, dissolution testing and has knowledge of quality control and analysis.
Krevinko Resume
Renee Krevinko has over 4 years of experience as a Forensic Scientist at Quest Diagnostics, where she is responsible for instrument operation, sample analysis, result interpretation, and training colleagues. She has a Bachelor's Degree in Biology and minors in Chemistry and Forensic Science from California University of Pennsylvania and a Certificate in Forensic Science and Law from Duquesne University.
Caroline's CV 2015
Caroline Tedja Pranata has over 10 years of experience as a medical technologist in Singapore. She received her Bachelor of Science in Biotechnology from AtmaJaya Catholic University in 2009. Her thesis focused on detecting influenza virus from pediatric patients with diarrhea and influenza-like illness symptoms in Indonesia. Currently, she works as a medical technologist at National University Hospital, where she operates laboratory instruments and assists with laboratory accreditation. Previously, she gained experience at Jurong General Hospital and U.S. Naval Medical Research Unit-2 in Indonesia, operating various laboratory instruments and evaluating diagnostic test kits and reagents.
bhavana soni resume new
Bhavana Soni is seeking a challenging role in a laboratory environment, particularly in research and development, quality control, and regulatory affairs. She has a M.Sc. in Nutraceuticals and relevant work experience in laboratories at Mahanada Dairy and Vifor Pharmaceuticals. Her skills include laboratory techniques, safety practices, computer programs, effective communication, attention to detail, and the ability to work independently and as part of a team.
ramakrishna cv
This 3-page curriculum vitae outlines the qualifications and experience of Mr. Mutyala V A Ramakrishna. It includes his educational background, professional experience as a clinical research coordinator and site lead, previous participation in clinical trials from 2013 to the present, responsibilities and functional expertise, ICH GCP training, and signature. The CV provides contact information and demonstrates over 3 years of experience in clinical trials for various indications from Phase II to Phase III.
KK resume 7 th aug
Krishna Kumar Pandey is seeking a career in the pharmaceutical industry. He has a M.Pharma in Pharmaceutics from BITS Pilani with a 7.85 CGPA and a B.Pharma from B.B.D.N.I.T.M Lucknow with a 67.52%. He has experience with analytical instruments and software relevant to the industry. He completed a summer internship at Heron Parexel Company where he gained experience in systematic reviews. His projects involved development of drug delivery systems and evaluation of formulations. He held teaching assistant and volunteer positions where he demonstrated laboratory skills and maintained conduct. He achieved qualifying for GPAT with AIR 176 and completed online courses in I
JohnDiclericoJr_resume
John J. DiClerico Jr. is an experienced scientific leader with over 10 years of experience in molecular cell biology and biochemistry, focusing on oncology and Alzheimer's disease. He holds a Master's degree from Columbia University and has worked in quality control roles for several pharmaceutical companies, developing assays and ensuring compliance. He is currently a QC Associate Lead at Lifecell Corporation, where he oversees quality control testing and laboratory operations.
Roadmap for Drug Product Development and Manufacturing of Biologics.pptx
The development of therapeutic biologics involves a streamlined approach for their formulation and drug product development from early stages to process validation and commercialization.
This roadmap is based on experience with approved products and aims to improve safety, efficacy, and immunogenicity profiles in human patients, as well as maintain consistently high quality, efficiency, and reduced cost.
The approach should be applicable across all biotherapeutic products.
KVogt_resume8242014
Kristy Vogt has over 20 years of experience in laboratory science and quality assurance. She holds a Master's degree in Quality Assurance and Regulatory Science and has worked in roles managing laboratories and research evaluations. Her expertise includes food microbiology, infection control, and dental materials compliance.
RESUME
Mallikarjuna G currently works as a research associate in pharmacokinetics at Quest Life Sciences Pvt Ltd in Chennai. He has over 5 years of experience in areas like feasibility studies, clinical trial protocol design, clinical report writing, sample processing, and subject monitoring. He holds an MPharmacy in Pharmacology and has experience in areas like in vitro pharmacokinetic studies, pharmacological screening models, and analytical techniques like chromatography. He is skilled in MS Office, has published 3 research papers and 2 review papers, and has participated in workshops and seminars in fields like experimental pharmacology and molecular biology.
Susan E Pilipauskas v.3
Susan Pilipauskas is seeking a position as a scientist where she can utilize her skills to contribute to a laboratory. She has over 10 years of experience in various scientific roles at Abbott Diagnostics and Abbott Molecular, where she conducted research and testing, managed laboratory equipment and facilities, and adhered to regulatory standards. She holds a Bachelor of Science degree in Environmental Science from Benedictine University.
RyanSingh - CV1
This document is a resume for Ryan Singh, who has over 15 years of experience in research science and quality control chemistry. He currently works as a QC Chemist at AuroLife Pharma, where he performs testing on pharmaceutical products using various analytical techniques. Previously, he held research roles at Johnson & Johnson and Rider University, where he synthesized and tested lipid-lowering compounds. Singh has extensive lab skills and experience with FDA regulations, and he seeks to contribute his drive and expertise to support product quality assurance.
Nicholas W. Reynolds Resume
Nicholas W. Reynolds has over 10 years of experience in the biology field, currently serving as Manager of In-Vivo Research Services at Toxikon Corporation in Bedford, MA. He oversees 15 technicians and ensures study compliance. Previously he was a Supervisor and Technician, gaining skills in injections, surgical techniques, and pharmacokinetic studies using various animal models. He holds a B.S. in Biology from UMass Dartmouth and has presented research posters.
Similar to Buu Tu resume (20)
Roadmap for Drug Product Development and Manufacturing of Biologics.pptx
Roadmap for Drug Product Development and Manufacturing of Biologics.pptx
Buu Tu resume
- 1. Buu Tu 1505 Mifflin Street ● Philadelphia, PA 19145-2210 ● buutoantu@gmail.com ● 215-796-0778 OBJECTIVE: To apply my skills and knowledge of product formulation in a R&D laboratory position in the pharmaceutical industry. I am a natural problem solver who finds multiple solutions to any problem and will be a strong asset to a role that aims at creating effective products and efficient manufacturing processes. EDUCATION St. Johns University, Queens, NY Jan 2013 Masters of Science in Industrial Pharmacy, GPA 3.28/4.00 University of the Sciences in Philadelphia (USP), Philadelphia, PA June 2008 Bachelor of Science in Pharmaceutical Sciences, GPA 3.36/4.00 Central High School, Philadelphia, PA June 2004 EXPERIENCE Colorcon Inc. / Global Tech. Services - IR division, West Point, PA June 2008 – Dec 2008 Laboratory Technician • Assisted senior researchers in formulating immediate release tablet by performing physical stability evaluation studies using UV Spectrophotometry and operating laboratory equipment under laboratory GMP conditions (GMP conditions including using appropriate safety equipment, clothing, and keeping records of all experimental procedures and result) • Followed research plans and executed experiments necessary to achieve more efficient production methods • Multitasked 3 projects and increased the formulation deliverables to over double their typical quarterly goals. University of the Sciences in Philadelphia, Philadelphia,PA Fall 2006 – Spring 2008 Organic Chemistry Laboratory Teaching Assistant • Guided organic chemistry lab students in performing laboratory procedures. • Graded lab reports and laboratory techniques RELEVANT COURSEWORK EXPERIENCE • Performed Mammalian Cell Culturing and various analytical assays such as Trypan and Alamar Blue Assay, Bradford Protein Assay on adherent and suspension cells • Experienced in analytical chemistry and instrumental analysis RESEARCH St Johns University, Queens, NY Fall 2012 Department of Pharmaceutical Sciences / Dr. Bhagwan D. Rohera, Professor • Evaluated the physicochemical properties of OTC cold and flu liquid and suspension medications using basic analytical instruments such as Ostwald viscometer, 10mL volumetric flask, and analytical balance • Developed generic formulations of these innovator products University of the Sciences in Philadelphia, Philadelphia, PA May 2007– 2008 Pharmaceutical Sciences Department / Dr. K. Jonnalagadda, Assistant Professor of Pharmaceutical Sciences • Developed a formulation to increase the efficiency of encapsulating methylene blue in PLGA microspheres and evaluated results of the experiments using UV Spectrophotometry analysis • Maintained a healthy line of mammalian macrophage cell cultures by routinely replenishing growth medium and performing cell passages when necessary following aseptic techniques • Conducted Alamar Blue assays with data collected and analyzed using UV spectrophotometry INSTRUMENTATION ● Piccola Rotary Tablet ● Glatt Fluid Bed Granulator ● HPLC Press 8-10 station ● Glatt Drum Tablet Coater ● Centrifuge ● Alexanderwerk Roller ● Sotax Dissolution Bath ● Gas Chromatograph Compactor WP 120 Pharma ● Tablet Disintegration Tester ● Fluorometer ● High Sheer Wet Granulator ● UV Spectrophotometer ● Atomic Absorption Computer Literacy: Proficient in Microsoft Office tools (Word, Excel, Powerpoint) Foreign Languages: Cantonese (conversational) Honors and Activities: • St. Johns University AAPS – Student Chapter, Industrial Pharmacy Journal Club, Graduate Student Association • USP Merit Scholarship recipient, Deans List • USP Rifle Team, Asian Students Association, Pharmaceutical Sciences Club, Journal Club