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Full scope covered is therapeutic modalities of biologics and vaccines produced in mammalian cell culture and microbial systems like yeast, bacteria and baculoviruses. Develop and lead integrated teams of biotechnologists, biochemists, process engineers, and bioanalytical experts to develop innovative, competitive, cost-efficient, sustainable, environmentally friendly and efficient manufacturing processes delivering on Growth and Profitability of Sanofi's entire biologics business.
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Serve as a subject matter expert in cell line development to represent functional area for biologics pipeline programs. We are rapidly growing and seeking a talented individual for the role of Senior Research Scientist to join our Process Development team based on Hopkinton, MA. The successful candidate will be able to lead and execute laboratory procedures and perform stable cell line development and expression of recombinant proteins and antibodies to support manufacturing.
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The Director, Analytical Development will provide technical leadership and lead a team of analytical scientists in support of biologics clinical development programs. Demonstrated success in the development, transfer, qualification and validation of biologics based analytical methods using the ICH, FDA and EMA guidelines and regulatory requirements.
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The global Cell Culture Development (CCD) organization within Sanofi operates with the mission to develop robust, scalable and high productivity cell culture processes for Sanofi's very diverse early and late-stage biologics pipeline.
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Arteriocyte Medical Systems, Inc. (dba Isto Biologics) has an opening for the Senior Product Marketing Analyst position in Hopkinton, MA. Responsible for driving the analysis, planning, and development and evaluation of the business segments in both domestic and overseas markets to optimize profit and meet marketing, financial, and corporate growth objectives.
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Quality Assurance (QA) Operations is responsible for quality oversight of operations at Sanofi’s Framingham Biologics facilities. Provide expertise during procedure/SOP revision process and function as DCR approver for department related SOPs and PRs.
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Experience supporting biologics CMC regulatory submissions a plus. Experience supporting biologics CMC regulatory submissions a plus. Comfort with Microsoft Office (PowerPoint, Excel, Word, OneDrive) and electronic document management systems (Veeva, e.
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