yyyyyy x. yyyyyy 3 jackson hole unit #0000 xxxxxx xxxx , xxxx , xxxxx 00000
quality-focused research scientist eager to contribute expertise in biology, lab operations and project management toward supporting the employer in optimizing results.
ø b.s., biology.
ø seeking to utilize expertise in field biology area.
ø six years of successful career background in research science.
ø record of progression to assignments of increasing authority and responsibility.
ø expertise in sop, glp and cgmp.
ø knowledgeable in safety and regulatory compliance.
ø strong laboratory team player.
ø adept in analytical techniques and standardized laboratory testing methodologies.
ø capacity in identification/resolution of research issues.
ø consistent achievement of stringent project/production deadlines.
ø self-directed, self-motivated individual.
ø well-organized multi-tasker with strong detail orientation.
ø proficient in advanced business software applications and specialized databases including : analyst, mass lynx, watson, aria, chem station, empower, millennium windows, excel, powerpoint.
lc/ms, hplc, dsc, gc, ir, acquity™ uplc, multiprobe, tomtec™, protein precipitation, solid phase extraction, liquid/liquid, size exclusion chromatography, extraction, method development, report preparation, sop preparation, aseptic technique, cell culture, bacterial transformation, restriction analysis and digest, dna fingerprinting, protein gel electrophoresis, pcr and use of a thermocycler, dna extraction, protein purification, bioburden, population determination, neutralization validation and micro limit tests.
taxolog, inc., fairfield, nj 2007 - present
analytical research scientist
recruited to perform procedures in compliance with sop, glp and cgmp, safety and regulatory requirements.
effectively coordinate with laboratory personnel to achieve critical project timelines, specifications and objectives.
originate assays based on new/existing methodologies including hplc, uplc™ and gc.
effectively validate testing methodologies for raw materials, production intermediates and final products.
play key role in set-up of new/existing methods for identifying compounds, validation and documentation.
perform in-depth separation/characterization of protein drug candidates, formulation development, peptide mapping and related analytical development methods.
deliver well-received analysis/evaluation of material and products at all stages of development process.
utilize judgmental capacity conforming to defined practices and policies in selecting methods and techniques for obtaining solutions.
- continued -
yyyyyy x. yyyyyy
schering-plough research institute, lafayette, nj 2005 - 2007
retained to maintain documentation, notebooks and data books.
performed bioanalytical projects in compliance with fda regulations.
developed and validated new bioanalytical assays.
conducted method preparation and validation.
prepared and analyzed study samples in accordance with sop, glp and cgmp regulations.
gained expertise in use of modern methodology/technology including hplc, uplc™, gc, lc/ms ms, multiprobe and tomtec™.
utilized such advanced applications as analyst, watson, mass lynx and aria.
assumed responsibility for troubleshooting/monitoring instrumentation and assay problems.
planned and organized project workload.
reviewed scientific validation reports, analytical portions of research reports and regulatory submissions.
disseminated data to appropriate colleagues.
originated and published scientific data and information.
developed and presented bioanalytical compound information to compound directors and department heads for ind submission.
effectively trained bioanalyst for method development, validation and sample analysis.
formulated timelines for assigned projects.
geo-centers inc., picatinny arsenal, nj 2004 - 2005
brought into organization to test solid propellants using hplc, gc and nir ir to determine stabilizer level.
consistently utilized stringent quality control requirements.
conducted dsc thermal technique to determine measured difference in energetic materials energy.
attained compliance with all epa regulations.
delivered support to perform quantitative analysis on propellant degradation products.
utilized multiple laboratory instruments to assess stability of u.s. army ardec stockpile assets globally.
ensured use of approved safety methods for handling energetic materials and hazardous waste streams.
developed thorough knowledge of ardec safety and security regulations.
aided in performance of quantitative analysis on propellant degradation products using laboratory instruments to assess stability.
prior to 2004, served as group leader, marypaul laboratories, inc., sparta, nj, and supervisor, willowglen academy, sparta, nj. in these assignments, built outstanding biological laboratory operations, quality assurance, media preparation, microbiological preparation, culture, testing, supervisory and field sampling skill sets.
east stroudsburg university, east stroudsburg, pa
bachelor of science, biology, 2004
Remember: Hire Us To Write YOUR New Resume
And We GUARANTEE That If You’re Not Working In 60 Days Or Less,
We’ll Revise Your Resume, Refund Your Money,
AND Give You $50 EXTRA!