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yyyyyy x. yyyyyy

(xxx-xxx-xxxx • abc@xyz.com

 

 

profile of qualifications

 

details-focused quality control specialist eager to offer 20+ years of solid quality assurance, testing / scheduling, regulatory compliance, process improvement, and data documentation / management experience toward maximizing a progressive employer s product research and manufacturing success.  top-performer who can guarantee superior levels of quality control toward achieving optimal product results.  ambitious self-starter who demonstrates high-level proficiency with usp standards and gmp / glp requirements.  excellent communicator who can plan, prioritize, and manage multiple tasks within deadline-driven environments.

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key technology summary

 

chromquest • dissolution-time release • drug-coated stents • viscometer colorimeter • testing-gel electrophoresis • karl fisher

gc / ir / uv / vis • particle size • data analysis / graphs • dsc tga cation / anion analysis • totalchrom • smartlab

high-performance liquid chromatography (thermo finnigan) • laboratory information management system (lims)

folin lowry protein analysis • pcr-elisa • lotus software (approach / ami pro) • millennium software • peaknet

microsoft office • microsoft windows • internet applications

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professional synopsis

 

qc analyst analytical lab

astrazeneca, westborough, ma                                                                                                                                                   2004 c 2009

 

         applied dynamic analytical abilities toward logging qc samples for testing to include effectively planning, prioritizing, and scheduling testing activities to maximize use of resources and meet key laboratory objectives.

         complied with set fda guidelines to accomplish required qc tasks, along with proactively revising sops as necessary.

         expertly calibrated and troubleshot testing equipment to ensure seamless analytical laboratory processes at all times.

         played a vital role in sustaining safe and productive laboratory environments by serving as a safety volunteer.

 

r&d lab drug discovery

atrium medical, hudson, nh                                                                                                                                                                       2003

 

         strategically steered drug discovery efforts by testing various polymers for coated stents utilizing hplc; comparing noted results; and organizing graph-based reports to include proficiently coordinating testing processes with production department.

 

quality control lab

epoxy technology, inc., billerica, ma                                                                                                                                         2000 c 2002

 

         utilized broad scope of qc, analytical instrumentation, and glp knowledge to test and review raw materials and finished products by employing a wide range of tools, i.e. dsc, tga, ir, particle size, cation / anion analysis, viscometer, colorimeter.

         optimized qc lab processes by developing comprehensive testing procedures and validating equipment.

 

analytical chemistry

muro pharmaceutical, inc., tewksbury, ma                                                                                                                                           2000

 

         drove pharmaceutical processes efficiency by coordinating the chemical analysis of raw materials, in-process samples, finished products, and stability samples via the use of established lab methods and techniques.

         achieved superior testing results by following usp methods, gmp / glp requirements, and lot release protocol, along with maintaining and monitoring state-of-the-art equipment to guarantee optimal product reliability rates.

 

qc associate

bd biosciences, bedford, ma                                                                                                                                                                    2000

 

         met and / or exceeded qc goals by independently carrying out routine testing on raw materials, in-process products, and finished goods utilizing set sops to include logging incoming products, scheduling testing, and reporting critical results.

 

additional job history

 

senior qc coordinator, opta food ingredients, inc., bedford, ma                                                                                      1993 c 1998

senior qa technician, c.r. bard, inc. critical care division, tewksbury, ma                                                                 1989 c 2002

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education

 

b.s., food science                                                                                                                                               university of rhode island

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