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This candidate will be expected to have a breadth of cell-based assay and in vitro pharmacology expertise to support drug discovery projects from hit identification through lead optimization.
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Our client, one of the largest Pharma companies in the U.S., is looking for a Investigator, MS&T (Manufacturing Science and Technology) which is located at Princeton NJ. Looking for MS&T Specialist to provide technical support and expertise in gene/cell therapy manufacturing processes.
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Our commitment to diversity, equity, and inclusion. For more than 20 years, its passionate, innovative and collaborative team has invented next-generation antibody technology platforms and leveraged translational research and data sciences, which has resulted in a proprietary pipeline including bispecific T-cell engagers, next-generation immune checkpoint modulators, effector function enhanced antibodies and antibody-drug conjugates.
$343,750 a yearFull-timeExpandApply NowActive JobUpdated 14 days ago - UpvoteDownvoteShare Job
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Strong tactical familiarity with the design, overseeing and assessment of clinical trials and with other MA tools (expertise in clinical trial methodology and conduct, GCP principles, medical product support activities, publications, ISS, med ed) Subspecialty training in relevant therapeutic area preferred (Sickle Cell/Hemoglobinopathies) We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.
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Dsm-firmenich is fully dedicated to inclusion because when people feel engaged and empowered, their creativity and innovation drives unprecedented progress. Diversity, Equity & Inclusion is a shared responsibility woven into our daily work to not only benefit our People, Customers & Communities but also drive business value.
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The ideal candidate for this position should have work experience in cell therapy process development, manufacturing science, analytical development, and familiarity with GMP/FDA/ICH guidelines.
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Validating equipment and processes, including bioreactor Installation Qualification (IOQ) and Performance Qualification (PQ) studies, and other cell culture validation activities.
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Equipment validation (bioreactor IOQ and PQ study, but not limited to the other cell culture validation activity). The Cell Culture Manufacturing Senior Technician position will directly enable the initial start-up phase of the Hopewell manufacturing facility and then shift focus to hands-on execution and support of cGMP manufacturing operations.
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From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.
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Familiarity with practices of and intersections between commercial sales, marketing, medical affairs, and market access organizations in the pharmaceutical industry. Working knowledge of relevant US pharmaceutical compliance guidelines, regulations (AKS, FCA, FDCA, HIPAA, FCPA) and PhRMA Code principles.
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We are focusing our collective efforts to advance sustainability, equity, and trust that come to life through our core commitments. Subject matter expertise in a financial services sub-area like Retail Banking, Commercial Banking, Transaction Banking, Wholesale Banking, Cards & Payments, Wealth Management, Investment Management, Real Estate, Private Equity, Capital Markets.
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Stay updated with advancements in cosmetic science and technology. 2-3 years experience in the cosmetic industry, preferably in product formulation and development. Familiarity with industry-standard laboratory practices and Good Laboratory Practices (GLP) preferred.
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We are deeply committed to our Diversity, Equity and Inclusion efforts, and we warmly welcome job applicants of all backgrounds. The base salary offered will take into account internal equity and may vary depending on the candidate's geographic region of work premises, job-related knowledge, skills, and experience among other factors.
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Serve as subject matter expert for residual DNA by qPCR, host cell protein ELISA, Residual Protein A ELISA, binding activity ELISA, Capillary Electrophoresis (CE), and capillary isoelectric focusing electrophoresis(cIEF), including qualification, assay validation and transfer activities.
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Assist with the development and execution of value communications initiatives for franchise, including non-branded and branded initiatives – examples include but are not limited to, unmet needs & payer value story, working with an agency, learning the Promotional Review Board (PRB) process and usage of VEEVA, developing & testing value messages, generating Real World Evidence (RWE) to support the payer value proposition.
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equity and inclusion non cdl cell phone jobs Title: sales representative in Rocky Hill, NJ
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