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Our department (Vaccines and Advanced Biotechnologies, VAX) Process R&D is responsible for the development and clinical manufacturing of Drug Substance (DS) and Drug Product Intermediates (DPI) for the vaccine and advanced therapy pipeline, spanning from preclinical to commercialization stages.
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The US Process Analytics group (part of the GSK Research and Development division) is responsible for developing mechanistic, data driven, and hybrid models to support the design, development, and manufacturing of biopharmaceuticals (both drug substance and drug product.
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These individuals must have a scientific background in either a CMC discipline (i.e., Supply Chain, Drug Substance, Drug Product or Analytical) or safety/DMPK within the pharmaceutical industry.
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Preferred Qualifications:If you have the following characteristics, it would be a plus:Experience delivering a late stage drug substance technology transfer, with an understanding of the product development process.
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The Mobile Integrated Health ("MIH") Specialist functions as a core member of the Mobile Integrated Health Program within the Department of Public Safety and works collaboratively with multiple offices and departments throughout the County to address the issues of complex patients who use the Emergency Department for the treatment of substance use and behavioral health disorders.
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The ASR includes crime statistics and institutional policies concerning campus security, such as those concerning alcohol and drug use, crime prevention, the reporting of crimes, sexual assault, and other matters.
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Principal Scientist, Sterile Drug Product Commercialization. Serve on cross functional drug product (DP) working group and supports LVV lyophilized DP activities through filing and Process Performance Qualification (PPQ), site characterization plan and execution, tech transfer control strategy, process development, PPQ readiness, PAI (Pre‐Approval Inspection) readiness, approval, launch and post‐launch support.
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Partner with API Protein, API CGT, and Drug Product development teams to define relevant material selection, assessments, and control strategies. Use of this site constitutes your consent to application of such laws and regulations and to our.
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The successful candidate will utilize his/her experience in biopharmaceutics/modeling, and use biopharmaceutics knowledge created using integrated in-vivo, in-vitro and in-silico (physiologically based pharmacokinetic/ biopharmaceutics modelling) tools to design and develop the most suitable drug product that is fit for the patient and meets the development timelines.
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Where permissible by state law, certification to use heavy equipment requires successful passing of a drug test. The employee is often required to use their hands and fingers, to handle or feel.
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The role of Research Scientist, Drug Delivery & Nanotechnology involves leading and conducting experiments for the discovery and preclinical activities of Ocugens product pipeline related to nanoparticle-based drug substances.
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Develop and deliver domestic violence-related training for medical personnel /facilities, substance abuse, behavioral health, and allied health professionals in Montgomery County. Serve as a representative for Laurel House in coordinating contacts with hospitals, substance abuse facilities, behavioral health facilities, and medical facilities in Montgomery County so that these systems will view the agency as a resource for training about domestic violence as well as a resource for patients who may be experiencing DV.
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MS in Pharmaceutical Science with job related experience in the field of drug development and clinical pharmacology. Develops new innovative and impactful clinical pharmacology approaches to processes and drug development strategies and can assemble a multidisciplinary team to execute the components of clinical pharmacology program.
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ServiceNow Developer with preferred experience in the Third Party Risk Management (Vendor Risk Management) use case. This role will focus on the build out of the Third Party Risk Management (formerly Vendor Risk Management) use case and capabilities in Vanguard's existing ServiceNow environment.
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These duties will include directing the development of small molecules, drug substance outsourced programs, enabling cGMP manufacturing for commercial or clinical use. This position will lead, manage the development of chemical process for active pharmaceutical ingredients (APIs), process scale-up, technology transfer, and validation activities that are outsourced (domestic and international contract organizations) by Harmony to support uninterrupted supply of pharmaceutical drug substance of the highest quality for our patients.
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