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Posted on : 22 December 2017
The qualified candidate will join the Bioassay and Impurities Testing group, which is part of the Analytical R&D organization located in Andover, MA, to enable the development of biological therapeutics at Pharmaceutical Worldwide Research and Development. The candidate will be part of a highly matrixed team responsible for developing analytical methodologies and strategies needed to progress biotherapeutic products through the pipeline, with an emphasis on impurity testing. This includes routine sample testing, most notably for Host Cell Protein, Residual Protein A, and Host Cell DNA, as well as method development and qualification. The candidate should have experience with ELISA and/or qPCR. Experience with method development, method validation and familiarity with cGMP practices is desired. This position will provide routine analytical testing using established methodologies and develop skills necessary to support method development and validation. The ideal candidate will have experience using some or all of the above analytical methodologies for the analysis of biologics and have proficiency in Microsoft Office software such as Excel and Powerpoint. In addition, the candidate should have good documentation skills and will be expected to tabulate and provide data interpretation to their team and to their customers. The candidate must excel at working in a collaborative, highly matrix fast-paced environment.
MA - Andover
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