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The Quality Assurance Operations Engineer DSM is responsible to help drive the Quality oversight for the direction of all Drug Substance Manufacturing processes through to operational readiness during project phase.
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WingSwept is seeking an Application System Administrator within our application development division, to provide both internal and external technical support for our web-based Case Management and Tracking System (CMTS) as well as other key applications within the company.
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Thats why we offer competitive wages and a wide range of benefits, including medical and dental insurance, prescription drug card, 401K and pension plans, flexible dependent care and medical spending accounts, spouse and child life insurance, employee referral bonus, and discounts with Penske partners.
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The QC Analytical Development (AD) Chemistry Scientist 2 is responsible for coordinating the transfer of analytical methods for Technology Transfer (TT) of drug substance (DS) and drug product (DP) into the Quality Control laboratories of FUJIFILM Biotechnologies Diosynth Holly Springs (FDBN.
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HVAC Certification (CFC certification) & CPO Must have reliable transportation and valid driver's license Ability to pass pre-employment criminal history & drug screen. Kane is focused on creating places with large-scale, mixed-use development, multi-family, office, hotel and retail projects.
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In this vital role you will be a part of the Process Development Drug Substance Technology group at Amgen’s FleX Batch Biologics Manufacturing Facility. Engineer Upstream, Process Development.
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The FleX Batch facility will not only feature the best in-class drug substance manufacturing technologies with embedded Industry 4.0 capabilities, but it will also integrate sustainability innovations to reduce carbon and waste, as part of Amgen's plan to be a carbon-neutral company by 2027.
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Amgen, one of the worlds leading biotechnology companies is investing $550 million to build a new multi-product drug substance biomanufacturing facility in Holly Springs, North Carolina, a biomanufacturing hub known for their life sciences industry.
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Prior drug substance and commercial manufacturing experience, including late stage process development, validation, and tech transfer. Provides Upstream / Cell Culture technical support for troubleshooting, process assessments, and execution of root cause analysis (RCA) and corrective and preventive action (CAPA) in response to process deviations.
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In this vital role you will work to provide scientific and technical contributions within Process Development Attribute Sciences at Amgen’s FleX Batch facility. Responsibilities include effectively delivering to the site, process development team, and quality control through rapid and robust analytical testing.
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The Process Development Associate will help design and perform experiments at the bench scale that span the end-to-end Drug Substance process, covering cell culture and/or purification operations.
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In short, to be the partner of choice in drug development. 2-5 years' experience in medical device clinical research Industry required 2-5 years' experience managing Cardiovascular device trials preferred Knowledge of ICH/GCP/FDA and other country specific regulations and guidelines for medical devices and/or pharmaceutical/biologic agents Proficient in computer applications such as MS Word, Excel, Publisher, PowerPoint Benefits of Working in ICON: Our success depends on the quality of our people.
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