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Yyyyyy x. yyyyyy

0000 xxxxxx xxxx , xxxx , xxxxx 00000 • (xxx-xxx-xxxx • Abc@xyz.com

 

Details-focused Quality Control Scientist / Study Manager eager to offer academic and professional credentials, as well as strong Strategic Analysis and Regulatory Compliance skills, toward maximizing a medical / biological employer s success.

 

Profile of Qualifications

 

         Integral leader who contributes precise, quality-oriented problem-solving abilities and solid troubleshooting techniques.

         Ambitious self-starter who plans, prioritizes, and manages multiple scientific tasks within deadline-driven environments.

         Top-performer who optimizes comprehensive laboratory data management practices to improve overall efficiency.

         Published abstracts and awards available upon request.

 

Professional Synopsis

 

Huntingdon Life Sciences, East Millstone, NJ                                                                                                       2006 C Present

 

Quality Control Scientist (2008 C Present)

         Apply sharp analytical abilities toward providing evaluation and quality control of pre-clinical and clinical sample analysis data for new drug development to include organizing and drafting technical materials and reviewing / revising immunoassay methods, as well as examining final reports, SOP deviations, and study file notes per GLP and FDA requirements.

 

Laboratory Coordinator (2007 C Present)

         Maximize laboratory productivity by cost-effectively ordering / receiving lab supplies and maintaining GLP quality lab standards, along with providing environmental monitoring (REES), equipment maintenance, and calibration as required.

         Proficiently serve as Co-Administrator of Molecular Devices SoftMax Enterprise v4.6 software and maintain all laboratory log books and archives, along with facilitating key audits and monitoring (TRACS) and SOP production and review.

 

Research Scientist (2006 C 2007)

         Drove research science success by performing ELISA immunoassays as necessary to include biomarker and sample analysis such as PK (pharmacokinetics), TA (total antibody), immunogenicity, titer, neutralization, and method validations.

         Demonstrated knowledge of GLP, GCP, Bloodborne Pathogen Safety Training, and RA Material Handling and Safety.

 

SGS Life Science Services, Fairfield, NJ                                                                                                                                            2006

 

Laboratory Technician Toxicology

         Expertly performed and / or supported cell line maintenance, media preparations, and in vitro testing of consumer products to include handling small animal weighing, dosing, and general care, as well as in vitro testing, SOPs preparation, and LIMS.

 

Montclair State University, Montclair, NJ                                                                                                                      2003 C 2006

 

Adjunct Professor / Laboratory Supervisor Department of Biology & Molecular Biology

         Utilized broad scope of industry and science knowledge to plan and present results-focused coursework (i.e. Biology of Human Life, Freshman Biology, Survey of Microbiology, Applied Microbiology) to biology, nursing, and other collegiate majors.

         Supported targeted academic efforts as an instructor for Weston Scholars and Gifted / Talented Summer Biology programs.

         Optimized educational success by instructing undergraduate students within a research lab environment on studies of cyanobacteria, cyanophage, and the effects of heavy metals on biological ecosystems, as well as the induction of cyanophage AS-1 from lysogenic to lytic life cycle via temperature, UV exposure, and mitomycin C.

         Prepared DNA libraries, DNA sequencing, and various microbiology and molecular biology techniques.

 

Education

 

M.S., Biology (4.0 GPA Thesis: The Genome of Cyanophage AS-1 )                                                        Montclair State University

 

B.S., Biology (Summa Cum Laude Minor in Chemistry)                                                                              Montclair State University

 

Technical Summary

 

Laboratory Techniques

Direct / Indirect / Sandwich ELISA (Endpoint & Kinetic) • Aseptic Techniques • Cell Culture / Cell Lines Maintenance

In Vitro Cytotoxicity Testing of Consumer Products (Agar Diffusion, Cell Viability Assays i.e. Trypan Blue, Irritection)

Small Animal Care / Handling • In Vivo Product Testing (i.e. Skin, Eyes, IP Injection) • Euthanasia • Necropsy

 

Microbiological Techniques

Bacteria Cultivation / Nutrition • Bacteria Stock Prep / Maintenance / Fermentation • Biochemical Testing • Growth Curves

Spectrophotometry (i.e. SpectraMax 384, 384 Plus, M5) • Viral Titering • Media Preparation • Sterilization • Biohazard Waste Disposal

 

Computer Skills

MS Office • Chromas • NCBI Basic Local Alignment Tools • Adobe Photoshop • LIMS (Watson 7.2) • SoftMax Pro Enterprise v4.6

 

Yyyyyy x. yyyyyy

0000 xxxxxx xxxx , xxxx , xxxxx 00000 • (xxx-xxx-xxxx • Abc@xyz.com

 

 

 

 

 

 

 

Date

 

 

Hiring Agent Name

Title

Company Name

Address

City/State/Zip Code

 

Dear__________________:

 

I am currently seeking a challenging [ Insert Job Title ] role, and am submitting my resume for your review.

 

I am excited to build a rewarding career with your company, and am confident that my broad range of academic and professional credentials, as well as proven Strategic Analysis, Quality Control, Regulatory Compliance, and Instructional / Laboratory Leadership experience, can achieve your key scientific objectives.

 

To complement my background, note that I hold an M.S. in Biology (4.0 GPA) and B.S. in Biology (Summa Cum Laude) from Montclair State University.  Please review my attached resume for a detailed account of my technical skills.

 

Currently, as a Quality Control Scientist / Laboratory Coordinator for Huntingdon Life Sciences, I apply my sharp analytical abilities toward providing evaluation and quality control of pre-clinical and clinical sample analysis data for new drug development to include organizing and drafting technical materials and reviewing / revising immunoassay methods, as well as examining final reports, SOP deviations, and study file notes per GLP and FDA requirements.  Within this role, I also maximize laboratory productivity by cost-effectively ordering / receiving lab supplies and maintaining GLP quality lab standards, along with providing environmental monitoring (REES), equipment maintenance, and calibration as required.  As this is just a sample of my job history, please kindly refer to my enclosed resume for additional experience.

 

You will find me to be a solutions-focused professional who can contribute superior attention-to-detail and solid problem-solving proficiencies.  In addition, I can plan, delegate, and manage multiple tasks within high-pressure, deadline-driven environments while streamlining scientific processes to increase productivity, efficiency, and quality.  For the sum of these aforementioned reasons, I believe I will prove to be an incredible asset to your team.

 

I look forward to hearing from you, and thank you in advance for your time and consideration.

 

Sincerely,

 

 

 

Yyyyyy x. yyyyyy

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