Tekwissen

TekWissen Group is a workforce management provider throughout the USA and many other countries in the world.. Conduct non-routine analysis of raw materials, intermediates, and finished product samples.. Conduct Quality Control Analtyical testing (e.g., ELISA, Flow Cytometry, PCR) of patient samples, stability samples, controls, and reagent qualification in a GMP environment.. Operating since 2009, we draw upon more than a decade of staffing experience to deliver critical talent acquisition solutions and IT engagements for our clients.. Our global footprint covers six countries: United States, Canada, Australia, India, United Kingdom and the Philippines.

research associate ii

Overview TekWissen Group is a workforce management provider throughout the USA and many other countries in the world. The below job opportunity is with one of our Biotech clients who researches develop and commercializes drugs. The company focuses primarily on antiviral drugs used in the treatment of HIV, hepatitis B, hepatitis C, and influenza, including Harvoni and Sovaldi. Position: Quality Control Research Associate - II Location: Santa Monica, CA 90404 Duration: 6 Months Job Type: Contract Work Type: Onsite Description All of previous level plus: <ul><li>Conduct non-routine analysis of raw materials, intermediates, and finished product samples. </li><li>Troubleshoot instrumentation and test methods. </li><li>Assists in the training of QC staff as needed. </li><li>Applies knowledge of current Good Manufacturing Practices (cGMPs) and Good Laboratory Working knowledge and proficiency with Microsoft Office software. </li><li>Writes and executes protocols and reports. </li><li>Evaluates equipment for purchase and performs installations and qualifications of the new instruments. </li><li>Conduct Quality Control Analtyical testing (e.g., ELISA, Flow Cytometry, PCR) of patient samples, stability samples, controls, and reagent qualification in a GMP environment. </li><li>Perform reviews of assays and maintain laboratory in a state of compliance. </li><li>Troubleshoot instrumentation and test methods. </li><li>Assists in the training of QC staff as needed. </li><li>Applies knowledge of current Good Manufacturing Practices (cGMPs) and Good Laboratory Working knowledge and proficiency with Microsoft Office software. </li><li>Writes and executes protocols and SOPs. </li></ul>Most Important Part <ul><li>Conduct Quality Control Analtyical testing (e.g., ELISA, Flow Cytometry, PCR) of patient samples, stability samples, controls, and reagent qualification in a GMP environment. </li><li>Perform reviews of assays and maintain laboratory in a state of compliance. </li></ul>TekWissen® Group is an equal opportunity employer supporting workforce diversity. TekWissen is an emerging global human capital, recruitment and IT services organization. Operating since 2009, we draw upon more than a decade of staffing experience to deliver critical talent acquisition solutions and IT engagements for our clients. We’re founded on a culture that is passionate about delivering tailored solutions, that create lasting partnerships. Our global footprint covers six countries: United States, Canada, Australia, India, United Kingdom and the Philippines. This allows us to work in close partnership with organizations and manage everything from global talent needs with demanding resourcing strategies, to single sites with lower recruitment volumes. TekWissen® is an equal opportunity employer supporting workplace diversity.

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