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This person will join a fast-paced, collaborative, and multidisciplinary team to support bioreactor process development (perfusion and intensified fed-batch) at the bench and pilot scale for the advancement of low-cost biotherapeutics manufacturing.
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Proven expertise in downstream process development for viral vectors, with a focus on AAV and lentiviral vectors. Startup is searching for a team-oriented Scientist II, Downstream Process Development (Viral Vector) to join company's Viral Vector team to support the process development of novel cell and gene therapies.
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The Senior Scientist I will play a key role in the developing downstream purification process development for various modalities such as mAbs, ADCs, bio-specifics, gene therapy, etc.
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Just - Evotec Biologics' Bioreactor Process Development group is seeking an enthusiastic and hardworking team member who is passionate about expanding worldwide access to biotherapeutics through the advancement of continuous bioprocessing technology and mammalian cell culture processes.
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As a scientist in the Purification Development group, you will identify and develop new purification technologies, work to design optimized downstream drug substance processes for new biologic candidates, employ strategic thinking to overcome technical hurdles and oversee process technical transfer to GMP manufacturing facilities, as they make their way from discovery to the clinic and eventually commercialization.
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Transfers and Introduces technology of cell therapy-based and therapeutic protein processes into manufacturing collaborating extensively with Scorpion’s Process Development group to develop cGMP-compliant, clinical-scale production processes.
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We are seeking a Process Development Engineer I to join our Synthetic and Bioconjugation Scale-up Technologies (SBST) group as a part of our Preclinical Manufacturing & Process Development (PMPD) department.
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Downstream biologics process development technology transfer, scale-up and ongoing manufacturing of biologics (cGMP) including technical support for nonconformance investigations and other commercial support activities.
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15-year industrial working experience as a commercial-scale process unit engineer, process design engineer, separations process development engineer is required within any of the following industries: petroleum refining, petrochemical processing, chemical processing, renewable energy, bio-energy.
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Reporting to the Pilot Plant Manager, the Pilot Plant Associate will participate in upstream and downstream areas of AAV development in the Pilot Plant for new gene therapy programs and processes.
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60 months of experience working with agencies and transform the data into agency format for downstream agencies like RT cluster (DTF17, DTF716), CS Cluster (CE200), HS Cluster (NYS100) to process the data that are received from ACCELA, DECAL, NYBE systems that utilize technologies in Oracle Service Cloud, Oracle SOA, Oracle OPA and COTS- Accela product.
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(Global Oil Gas) Business Development Specialist - PIMS LP (Process Integration And Modeling System)
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The Downstream segment focuses on refining, logistics, power generation, and the marketing of crude oil, petroleum and petrochemical products, and related services to international and domestic customers.
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Ability to manage complex issues and the ability to apply this knowledge in a practical manner, and/or understand key aspects of standards development process and possess a familiarity with the work and organization of other industry-related standards developing groups (such as ANSI, ASME, ASTM, IEEE, ISA, IEC/ISO, AGA and GPA.
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(Global Oil Gas) Business Development Specialist - PIMS LP (Process Integration And Modeling System)
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The Upstream segment includes crude oil, natural gas and natural gas liquids exploration, field development, and production. Manage the interface and interaction between the Government Engagement, GHG (Greenhouse Gas) Abatement, Finance Readiness Workstreams, and Project Development Group.
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Iovance Biotherapeutics is an immuno-oncology company focused on the development and commercialization of novel cancer immunotherapies based on tumor infiltrating lymphocytes (TIL). Develop a Subject Matter Expert (SME)-level understanding of and be able to skillfully execute as well as troubleshoot Iovance’s GMP cell therapy manufacturing process(es.
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