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The Process Engineer will lead chemical process development projects to scale-up the synthesis of next generation battery materials technologies. Applying DOE and statistical analysis to process development.
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Must have detailed knowledge of clinical drug development process including working knowledge of GMP, 21CFR and Annex 13 requirements, GCP, ICH guidelines, Good Clinical Practices (GCPs) as well as guidelines for CTM labeling, packaging and distribution operations.
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We are looking for a self-motivated Packaging Simulation Engineer who is proficient in FEM simulation with multi-year FEM software ANSYS or ABAQUS. This position requires someone familiar with development process of simulation and characterization projects, that thrives in a multifaceted collaborative organization.
ExpandApply NowActive JobUpdated 23 days ago - UpvoteDownvoteShare Job
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Complete audits to assess accuracy and quality of scientific data submitted to the regulatory agencies in support of in vivo medical devices and in vitro diagnostic devices' application. QualificationsTo be considered for this role, you’ll require a minimum of 5 years of professional experience in relevant field of healthcare products or related activities e.g.:Work in medical devices industry and/or in vitro diagnostic devices(preferred) or closely related industries (e.g., pharmaceutical industry) such as research and development, manufacturing, quality management, regulatory affairs.
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The Real World Evidence (RWE) Organization: The Chief Medical Affairs Office’s RWE organization is responsible for establishing global scientific leadership and stature through the generation of integrated CMAO observational real-world evidence serving all therapeutic areas from post-proof of concept (POC) trials through Loss of Exclusivity (LOE) for priority pipeline candidates, pipeline supplementation through business development, and marketed inline products.
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Proficiency with numerical simulation software tools and expert in Matlab and/or Scientific Python. Able to perform independent research and development work. Hands-on experience of major FEM tools (e.g., ANSYS, ABAQUS, Hypermesh, etc.
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Founded in 2004, Pharmaron has invested in its people and facilities, and established a broad spectrum of research, development and manufacturing service capabilities throughout the entire drug discovery, preclinical and clinical development process across multiple therapeutic modalities, including small molecules, biologics and Cell & Gene Therapy products.
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Familiarity with ADME/PK concepts and drug development process and interfacing with regulatory teams would be desirable. Strong Expertise with invitro, cell-based assay development and optimization and proficiency with Cell culture, molecular biology techniques, ELISA, flow-cytometry, western blot, qPCR, single-cell cloning, immunohistochemistry and related protocols.
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Scientific Research Corporation (SRC) is looking for a Senior Cybersecurity Engineer to participate in a team tasked with providing Naval Information Warfare Center (NIWC) Pacific with a broad range of cybersecurity capability- development, reviews, testing, training, threat and risk assessments, engineering process improvement and Assessment and Authorization (A&A) Services.
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Job Seekers with a Disability: Thermo Fisher Scientific offers accessibility service for job seekers requiring accommodations in the job application process. Lead Process Analytical Market development.
$80,000 - $110,000 a yearFull-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Collaborate with Business Development and scientific leadership of DMPK to identify, pursue, and close new opportunities. PhD in pharmacokinetics, chemistry, biochemistry, or a related scientific discipline.
$120,000 - $150,000 a yearFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Job Description Scientific Research Corporation (SRC) is looking for a Senior Cybersecurity Engineer to participate in a team tasked with providing Naval Information Warfare Center (NIWC) Pacific with a broad range of cybersecurity capability- development, reviews, testing, training, threat and risk assessments, engineering process improvement and Assessment and Authorization (A&A) Services.
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The Director of Drug Metabolism and Pharmacokinetics (DMPK) and Bioanalysis will oversee the scientific processes involved in conducting and executing in vivo pharmacokinetic (PK) studies, including associated bioanalysis and reporting/interpretation of PK parameters.
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Experience and expertise with antibody and/or peptides compounds, including biologics upstream and downstream process development, formulation of injectable and intramuscular biologics, process characterization.
$166,700 - $241,325 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Prior experience must include: Understand chemistry and biology to analyze data and discuss with other researchers to plan strategies for drug discovery projects; independently design and implement scientific research projects relating to the development of oligonucleotide therapeutics; perform and direct synthesis of organic molecules, including chemically modified oligonucleotides; plan assay designs and manage technicians, including both in-house and external CROs to execute them.
$67,900 - $223,200 a yearFull-timeExpandApply NowActive JobUpdated 15 days ago
process development scientific jobs in San Diego, CA
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