Artech Information System LLC
Bench Scientist
Artech Information System LLC, Chesterfield, Missouri, United States, 63005
Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost.Job Description
The qualified candidate will join the Bioassay and Impurities Testing group, which is part of the Analytical R&D organization located in Chesterfield to enable the development of biological therapeutics at Pharmaceutical.The position will be part of a highly matrixed team responsible for developing analytical methodologies (ELISA, qPCR) and strategies needed to progress biotherapeutic products through the pipeline.The scientist filling this position will work within a highly-matrixed team setting on a variety of modalities including vaccines, viral constructs, therapeutic proteins, and monoclonal antibodies. The contractor will work in a cGMP testing environment performing sample testing, method development, and method qualification.Qualifications
Work skills required: Experience with ELISA, and DNA techniques (qPCR), GMP.Intermediate proficiency in Microsoft Office (Excel, Word, and Outlook) is required. Must be able to understand and follow standard operating procedures.
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The qualified candidate will join the Bioassay and Impurities Testing group, which is part of the Analytical R&D organization located in Chesterfield to enable the development of biological therapeutics at Pharmaceutical.The position will be part of a highly matrixed team responsible for developing analytical methodologies (ELISA, qPCR) and strategies needed to progress biotherapeutic products through the pipeline.The scientist filling this position will work within a highly-matrixed team setting on a variety of modalities including vaccines, viral constructs, therapeutic proteins, and monoclonal antibodies. The contractor will work in a cGMP testing environment performing sample testing, method development, and method qualification.Qualifications
Work skills required: Experience with ELISA, and DNA techniques (qPCR), GMP.Intermediate proficiency in Microsoft Office (Excel, Word, and Outlook) is required. Must be able to understand and follow standard operating procedures.
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