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Job Title: Scientist Biology. The Scientist II is responsible for the development and evaluation of new reagents and testing new antibodies for use in flow cytometry applications. Analyze data using FCS Express and FlowJo software, report test results including completion of all required documentation and database entries as required by protocols or operating procedures.
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The Svendsen Lab at Cedars-Sinai Medical Center, Regenerative Medicine Institute is looking for a Project Scientist to join the team! Since 1902, Cedars-Sinai has evolved to meet the needs of one of the most diverse regions in the nation, setting standards in quality and innovative patient care, research, teaching and community service.
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Responsibilities will include a range of activities related to protein expression, purification, and cell line development; and the ideal candidate will be proficient in the design, optimization, and execution in transient and stable protein expression, multi-step purification, analytical data interpretation, troubleshooting and formulation of final product, while maintaining a highly productive and collaborative culture.
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Senior Scientist/Principal Scientist, Formulation and Process Development. We are currently searching for a highly motivated and innovative Formulation Scientist to joinour Formulation/Process Development team.
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Meet's partnered with an exciting and growing biotech in San Diego for a Senior Scientist / Principal Scientist Analytical Development! Write experiment protocols, development, and data reports.
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Provide recommendations, and contribute to making informed decisions on experimental data, and on steps to move projects forward. Strong data and statistical analysis skills. Apply in-depth molecular biology knowledge and experience in the development of CRISPR-based molecular diagnostic assay systems, including development of enzyme reagents and assay workflows.
$105,000 - $135,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Top Tier BioPharmaceutical company looking to add a Principal Scientist to their dynamic Pharmacometrics team. We are seeking a skilled and qualified industrial scientist who has experience in planning and executing MIDD approaches to join us as a Principal Scientist.
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Stantec is looking for a Senior Wetland Scientist/Permitting Specialist to support a high-volume environmental services program for a large utility client. Senior Wetland Scientist/Permitting Specialist - ( 2300033F.
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Insmed is seeking a scientist with significant experience with mouse vivarium experiment management and execution. This scientist will be responsible for execution of preclinical mouse models of neuro and muscular genetic diseases with research preparations of therapeutic constructs, including mouse genotyping, dosing, functional analysis, and tissue collection.
$86,000 - $115,333 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Your role will involve overseeing a dedicated chemistry team, providing guidance, and meticulously reviewing data to ensure the quality and progress of our projects. Create optimization strategies for improving lead series physiochemical properties, in vitro ADME, and PK via hypothesis-driven medicinal chemistry design principles.
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Specific to CTC/PWC and MCC: training and perform quality assurance duties by reviewing medical documentation utilizing audit tools as outlined by County of San Diego Quality Management.
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As a Clinical Lab Scientist (CLS) you will be responsible for a variety of clinical laboratory testing, result review and recording. Licenses: CA Clinical Laboratory Scientist. Serve as a laboratory department quality representative as needed to ensure quality compliance in documentation and performance, document any new trending quality issues, and work with laboratory manager and other quality team representatives to address the trending issues.
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In this role you have the opportunity to At Philips, we’re looking for a highly qualified Lab Analyst / Metrologist to join our quality team within the San Diego site ( note that this role requires the individual to be on site 5 days a week.
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Work in close collaboration with colleagues in R&D Quality Management, operational units in Drug Development (Clinical Development, Clinical Operations, Data Management, Manufacturing, Medical Affairs, Laboratories, Pharmacovigilance, Regulatory Affairs, Translational Medicine, vendors (CSPs) and partners in GMP QA.
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Contributes to data governance and data quality best practices including design reviews, unit testing, code reviews, and continuous integration and deployment. Working knowledge of multiple data management domains such as data modeling, integration, warehousing, data quality, security, and governance.
$113,668 - $203,468 a yearFull-timeExpandApply NowActive JobUpdated 9 days ago
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