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SeraCare Life Sciences, Inc. |
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http://www.seracare.com
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Organization Description:
SeraCare Life Sciences develops, manufactures, and sells a broad range of biological based materials and services essential for the manufacture of diagnostic tests, commercial bioproduction of therapeutic drugs, and additional research applications in the biotechnology, pharmaceutical, and diagnostic industries. SeraCare's offerings include plasma-based therapeutic products, diagnostic products and reagents, cell culture products, specialty plasmas, in vitro stabilizers, and clinically annotated DNA, RNA, serum, and tissue specimens ethically collected from consenting donors with a variety of patient conditions. SeraCare Life Sciences, Inc. has created a closed-loop delivery system for diagnostic products that is unique in this industry. This delivery system allows the company to selectively collect the human blood, manufacture the final product, and deliver the finished product to the customer in one controlled process, thereby achieving better quality control and a faster delivery of the final product to the customer with complete traceability. SeraCare has two major business divisions: BioPharmaceutical, serving the therapeutic and research markets through three business units, and Diagnostics, serving the diagnostic test kit manufacture market through two business units.
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Position Descriptions:
Project Scientist, Immunology: Responsible for the management of Virology/Immunology Products/Services/R&D/cGMP Laboratory group of the Virology/Immunology department. Will include management of all product development and services/R&D related projects as well as acting as scientific resource to product development group. Will manage associated personnel and resources. Will be required to assist in the identification, writing, and submittal of government and/or industry contracts and grants. Qualified candidates will have a Ph.D. with a minimum of 4 years post-doctoral experience, or Masters Degree in Cell Biology, Cell Immunology, or related field, with a minimum of 7+ yrs experience beyond master’s training (approximately 10+ years total experience). Must have demonstrated expertise in his/her discipline, as well as solid understanding of current GMP and GLP standards. Excellent communication, interpersonal, organizational and multi-tasking skills required. Preference given to demonstrated success in attracting outside funding and excellent writing skills. In addition, must possess strong computer skills, preferably experienced with Microsoft Word, Excel, and Project. Excellent use of judgment and discretion required. Extended work hours may be necessary in order to meet business demands.
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