Job Search Results for data scientist
Jun 02, 2026
Birmingham, AL
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Materials Science & Engineering
|
Perm
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$75k - $80k (estimate)
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The Analytical Development Scientist is responsible for performing laboratory testing on raw materials, in-process samples, and finished products, as well as supporting stability studies and... validation activities for drug product development. This role operates in a cGMP environment and requires a strong understanding of pharmaceutical regulations and analytical best practices.Key Responsibilities-Perform routine analytical testing, method validation, and process validation in accordance with SOPs, cGMP, GLP, GDP, and regulatory guidelines (FDA, DEA, OSHA)-Follow applicable compendial and regulatory standards for analytical procedures, method development, validation, and transfer-Troubleshoot laboratory methods and instrumentation, including HPLC and UPLC systems-Utilize Empower 3 software to analyze, interpret, and report analytical data-Complete assigned work efficiently while maintaining a strong focus on safety, quality, and timelinesWe are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com.To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/.
Aug 01, 2024
Cincinnati, OH
|
Claims/Denials
|
Contract-to-perm
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$24 - $30 (hourly estimate)
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A top personal care company is seeking a R+D Scientist who will participate in cross-functional meetings to develop and support various projects, coordinate and design studies to support product... claims, and ensure all product claims comply with global regulations. Candidate will review product artwork to ensure communication matches data, analyze study results to brainstorm communication strategies, and listen to consumer data focus groups to gather insights. The specialist will also conduct update meetings to ensure team alignment and write defensives about product claims.Preferred candidates will have the ability to assess risk based on technical data and navigate gray areas, strong computer skills including proficiency in Word, Excel, and PowerPoint, excellent communication skills, and the ability to work effectively in a team and matrix environment. The day-to-day activities for this role will vary, including participating in cross-functional meetings, coordinating studies, reviewing artwork, analyzing study results, listening to consumer focus groups, designing studies, conducting update meetings, and writing defensives about claims.We are a company committed to creating inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity employer that believes everyone matters. Qualified candidates will receive consideration for employment opportunities without regard to race, religion, sex, age, marital status, national origin, sexual orientation, citizenship status, disability, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to Human Resources Request Form. The EEOC "Know Your Rights" Poster is available here. To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/ .
Jun 16, 2026
Sanford, NC
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Engineering (Non IT)
|
Contract
|
$46 - $57 (hourly estimate)
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We are seeking a Method Transfer Scientist to support a high priority validation backlog within a pharmaceutical laboratory environment. This individual will play a key role in executing analytical... testing and supporting method transfer and validation activities across both vaccine and biologics programs (mAbs).This is a hands on lab role requiring strong technical expertise in HPLC and analytical testing, with the ability to contribute quickly after initial training.Key Responsibilities? Perform analytical testing using HPLC and related techniques? Support method transfer and validation activities across multiple projects? Execute testing for both vaccine and monoclonal antibody programs? Analyze and interpret data from laboratory experiments? Complete technical documentation and reports in alignment with GMP standards? Operate and troubleshoot laboratory instrumentation? Collaborate with cross functional teams to meet project timelines? Maintain high standards for data integrity and complianceDay to Day Breakdown? Approximately 75% hands on lab work? Approximately 25% documentation and reportingWe are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com.To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/.
Jun 15, 2026
Raleigh, NC
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Engineering (Non IT)
|
Contract
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$44 - $55 (hourly estimate)
{"JobID":541504,"JobType":["Contract"],"EmployerID":null,"Location":{"Latitude":-78.65,"Longitude":35.82,"Distance":null},"State":"North Carolina","Zip":"27612","ReferenceID":"RAL-66986330-b279-462e-a5ee-54c82f960fd9","PostedDate":"\/Date(1781536921000)\/","Description":"A global biopharmaceutical organization is seeking a Method Transfer and Validation Scientist to support the Quality Control organization within a regulated manufacturing environment. This individual will play a key role in transferring, validating, and maintaining microbiological test methods to ensure product quality, compliance, and operational readiness.This is a hands on laboratory role that requires strong experience with microbiology testing methods in a GMP environment.Key Responsibilities?Execute method transfer and validation activities for microbiological assays within a Quality Control laboratory ?Perform routine and non routine microbiology testing, including: ?Bioburden testing?Endotoxin testing?Sterility testing?Microbial identification as needed?Draft, execute, and review validation protocols, reports, and technical documentation?Analyze and interpret laboratory data to ensure accuracy, completeness, and compliance with regulatory requirements?Support investigations related to OOS, deviations, and assay performance and assist with root cause analysis and CAPA activities?Collaborate cross functionally with Quality Control, Quality Assurance, Manufacturing, and MSAT teams to support successful method transfers and process readiness?Update and maintain SOPs, test methods, and laboratory documentation to ensure continued compliance?Ensure all activities adhere to cGMP standards, data integrity requirements, and regulatory guidelines?Must be comfortable working either shift as follows: ?Shift A: Sun-Weds (4x10)?Shift B: Weds-Sat (4x10)We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com.To learn more about how we collect, keep, and process your private information, please review Insight Global\u0027s Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/.","Title":"Microbiology Method Transfer Scientist","City":"Raleigh","ExpirationDate":null,"PriorityOrder":0,"Requirements":"- 3-5 years of post-graduate relevant experience -Experience with various microbiology testing in the lab (Bioburden + Endotoxin is a must)-Experience working in a pharmaceutical setting -Experience supporting method validation, method transfer, or assay qualification activities","Skills":"","Industry":"Engineering (Non IT)","Country":"US","Division":"AF\u0026E","Office":null,"IsRemoteJob":false,"IsInternalJob":false,"ExtraValues":null,"__RecordIndex":0,"__OrdinalPosition":0,"__Timestamp":0,"Status":null,"ApplicantCount":0,"SubmittalCount":0,"ApplicationToHireRatio":0,"JobDuration":null,"SalaryHigh":55.0000,"SalaryLow":44.0000,"PayRateOvertime":0,"PayRateStraight":0,"Filled":0,"RemainingOpenings":0,"TotalOpenings":0,"Visa":null,"ClearanceType":null,"IsClearanceRequired":false,"IsHealthcare":false,"IsRemote":false,"EndClient":null,"JobCreatedDate":"\/Date(-62135578800000)\/","JobModifiedDate":"\/Date(-62135578800000)\/"}
A global biopharmaceutical organization is seeking a Method Transfer and Validation Scientist to support the Quality Control organization within a regulated manufacturing environment. This individual... will play a key role in transferring, validating, and maintaining microbiological test methods to ensure product quality, compliance, and operational readiness.This is a hands on laboratory role that requires strong experience with microbiology testing methods in a GMP environment.Key Responsibilities?Execute method transfer and validation activities for microbiological assays within a Quality Control laboratory ?Perform routine and non routine microbiology testing, including: ?Bioburden testing?Endotoxin testing?Sterility testing?Microbial identification as needed?Draft, execute, and review validation protocols, reports, and technical documentation?Analyze and interpret laboratory data to ensure accuracy, completeness, and compliance with regulatory requirements?Support investigations related to OOS, deviations, and assay performance and assist with root cause analysis and CAPA activities?Collaborate cross functionally with Quality Control, Quality Assurance, Manufacturing, and MSAT teams to support successful method transfers and process readiness?Update and maintain SOPs, test methods, and laboratory documentation to ensure continued compliance?Ensure all activities adhere to cGMP standards, data integrity requirements, and regulatory guidelines?Must be comfortable working either shift as follows: ?Shift A: Sun-Weds (4x10)?Shift B: Weds-Sat (4x10)We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com.To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/.
Apr 22, 2026
Upper Providence, PA
|
Engineering (Non IT)
|
Contract
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$52 - $65 (hourly estimate)
{"JobID":521917,"JobType":["Contract"],"EmployerID":null,"Location":{"Latitude":-75.45,"Longitude":40.18,"Distance":null},"State":"Pennsylvania","Zip":"19426","ReferenceID":"PHL-6a18ea1c-994d-4956-902d-753fb706b85f","PostedDate":"\/Date(1776873604000)\/","Description":"The Research Scientist will be supporting a high priority project within the Predictive Synthesis team in R\u0026D Discovery Chemistry. This individual will be responsible for executing high-throughput, nano-scale synthetic chemistry experiments using automated, plate-based workflows to rapidly generate high-quality experimental data. The role is highly hands-on and execution focused, requiring strong attention to detail, comfort with automation, and the ability to operate independently in a fast paced discovery environment.Key Responsibilities-Execute high-throughput synthetic chemistry experiments using automated, plate-based workflows (e.g., 1536-well formats).-Run nano-scale chemical reactions using liquid handlers, gloveboxes, and laboratory automation platforms.-Learn and execute predictive synthesis workflows to support discovery decision-making.-Deliver consistent experimental output, with expectations to complete two 1536-well plates per week (~3,000 data points).-Independently order reagents and building blocks required for experimental execution.-Accurately document experiments, results, and observations in the appropriate Electronic Laboratory Notebook (ELN) in accordance with internal standards.-Ensure data quality, reproducibility, and traceability across all experiments.-Collaborate with discovery chemistry and predictive synthesis teams to support project objectives.We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com.To learn more about how we collect, keep, and process your private information, please review Insight Global\u0027s Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/.","Title":"Scientist, Predictive Synthesis (Discovery Chemistry)","City":"Upper Providence","ExpirationDate":null,"PriorityOrder":0,"Requirements":"-3+ years of hands-on experience in synthetic chemistry with nano-scale, high-throughput experimentation in an academic or professional industrial setting.-Bachelor?s, Master?s, or PhD in Chemistry-Experience using laboratory automation platforms such as: Mosquito, Bravo, Tecan-Experience working with automation, liquid handling systems, or high-throughput laboratory workflows.-Familiarity with predictive, data-driven, or AI-enabled chemistry workflows.","Skills":"?Experience with ACD Katalyst electronic lab notebook ?Experience with Spotfire data analysis.","Industry":"Engineering (Non IT)","Country":"US","Division":"AF\u0026E","Office":null,"IsRemoteJob":false,"IsInternalJob":false,"ExtraValues":null,"__RecordIndex":0,"__OrdinalPosition":0,"__Timestamp":0,"Status":null,"ApplicantCount":0,"SubmittalCount":0,"ApplicationToHireRatio":0,"JobDuration":null,"SalaryHigh":65.0000,"SalaryLow":52.0000,"PayRateOvertime":0,"PayRateStraight":0,"Filled":0,"RemainingOpenings":0,"TotalOpenings":0,"Visa":null,"ClearanceType":null,"IsClearanceRequired":false,"IsHealthcare":false,"IsRemote":false,"EndClient":null,"JobCreatedDate":"\/Date(-62135578800000)\/","JobModifiedDate":"\/Date(-62135578800000)\/"}
The Research Scientist will be supporting a high priority project within the Predictive Synthesis team in R&D Discovery Chemistry. This individual will be responsible for executing high-throughput,... nano-scale synthetic chemistry experiments using automated, plate-based workflows to rapidly generate high-quality experimental data. The role is highly hands-on and execution focused, requiring strong attention to detail, comfort with automation, and the ability to operate independently in a fast paced discovery environment.Key Responsibilities-Execute high-throughput synthetic chemistry experiments using automated, plate-based workflows (e.g., 1536-well formats).-Run nano-scale chemical reactions using liquid handlers, gloveboxes, and laboratory automation platforms.-Learn and execute predictive synthesis workflows to support discovery decision-making.-Deliver consistent experimental output, with expectations to complete two 1536-well plates per week (~3,000 data points).-Independently order reagents and building blocks required for experimental execution.-Accurately document experiments, results, and observations in the appropriate Electronic Laboratory Notebook (ELN) in accordance with internal standards.-Ensure data quality, reproducibility, and traceability across all experiments.-Collaborate with discovery chemistry and predictive synthesis teams to support project objectives.We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com.To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/.
Jun 18, 2026
San Diego, CA
|
Materials Science & Engineering
|
Contract
|
$34 - $42 (hourly estimate)
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We are seeking a Scientist (non-PhD) to join our team. The candidate will join our interdisciplinary and highly collaborative team to support and advance our preclinical oncology drug pipeline. The... ideal candidate will have a strong background in cellular and molecular biology, in vitro pharmacology, and biochemical/cell assay development. They will design, plan, and execute studies to explore novel drug targets. They will implement new technologies to support drug discovery, interpret experimental results, and present their research. The successful candidate will have a proven track record of independent research experience with an ability to learn quickly and think critically. This position will provide the motivated candidate with ample opportunity for scientific growth through exposure to all aspects of the drug discovery process. Special consideration will be given for candidates that have expertise in cancer biology.We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com.To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/.
May 18, 2026
Atlanta, GA
|
Computer Engineering
|
Perm
|
$110k - $126k (estimate)
{"JobID":531211,"JobType":["Perm"],"EmployerID":null,"Location":{"Latitude":-84.37,"Longitude":33.77,"Distance":null},"State":"Georgia","Zip":"30308","ReferenceID":"ATL-f1276493-96ba-4810-8879-933ca37549d3","PostedDate":"\/Date(1779066010000)\/","Description":"In this role, the Data Engineer supports and builds end-to-end data pipelines across both on-premise environments (roughly 65% of the time) and the Azure cloud (about 35%), working as part of a small, collaborative team that includes two other Data Engineers and a Data Scientist. On a daily basis, they are designing, developing, and maintaining ETL workflows using SSIS?extracting data from various sources, performing data cleansing and validation, and integrating it into downstream systems to ensure accuracy and reliability. They also serve as an administrator within SSAS, building and maintaining data models, supporting analytical structures, and ensuring data is optimized and accessible for reporting and business intelligence. In close collaboration with the other engineers, they help troubleshoot pipeline issues, optimize performance, and share best practices across the data ecosystem, while partnering with the Data Scientist to ensure datasets are properly structured and readily available for advanced analytics and modeling. Additionally, they leverage Databricks to process and manage large-scale datasets, supporting more complex data transformations and analytics use cases. The role involves hands-on coding in Python and SQL to automate workflows, enhance pipeline efficiency, and manage operational tasks. While the majority of the work focuses on core data engineering responsibilities, there is also exposure to emerging tools like Microsoft Fabric and occasional work within Linux environments, contributing to a modern, evolving data platform.$110,000 to $126,000 - Exact compensation may vary based on several factors, including skills, experience, and education.We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com.To learn more about how we collect, keep, and process your private information, please review Insight Global\u0027s Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/.","Title":"Data Engineer","City":"Atlanta","ExpirationDate":null,"PriorityOrder":0,"Requirements":"?3-5 years in a Data Engineering role oSupporting and building data pipelines on prem (65% of the time) and Azure cloud (35% of the time)?SSIS (SQL Server Integration Services) for ETL, data cleansing and validation, data integration?SSAS (SQL Serve Analysis Services) - serving as an admin for data building data models?Experience with Databricks for large scale data?Coding experience with python and SQL","Skills":"?Experience with Fabric?Familiarity with Linux ?Experience building data pipelines in an GCP environment","Industry":"Computer Engineering","Country":"US","Division":"IT","Office":null,"IsRemoteJob":false,"IsInternalJob":false,"ExtraValues":null,"__RecordIndex":0,"__OrdinalPosition":0,"__Timestamp":0,"Status":null,"ApplicantCount":0,"SubmittalCount":0,"ApplicationToHireRatio":0,"JobDuration":null,"SalaryHigh":126000.0000,"SalaryLow":110000.0000,"PayRateOvertime":0,"PayRateStraight":0,"Filled":0,"RemainingOpenings":0,"TotalOpenings":0,"Visa":null,"ClearanceType":null,"IsClearanceRequired":false,"IsHealthcare":false,"IsRemote":false,"EndClient":null,"JobCreatedDate":"\/Date(-62135578800000)\/","JobModifiedDate":"\/Date(-62135578800000)\/"}
In this role, the Data Engineer supports and builds end-to-end data pipelines across both on-premise environments (roughly 65% of the time) and the Azure cloud (about 35%), working as part of a... small, collaborative team that includes two other Data Engineers and a Data Scientist. On a daily basis, they are designing, developing, and maintaining ETL workflows using SSIS?extracting data from various sources, performing data cleansing and validation, and integrating it into downstream systems to ensure accuracy and reliability. They also serve as an administrator within SSAS, building and maintaining data models, supporting analytical structures, and ensuring data is optimized and accessible for reporting and business intelligence. In close collaboration with the other engineers, they help troubleshoot pipeline issues, optimize performance, and share best practices across the data ecosystem, while partnering with the Data Scientist to ensure datasets are properly structured and readily available for advanced analytics and modeling. Additionally, they leverage Databricks to process and manage large-scale datasets, supporting more complex data transformations and analytics use cases. The role involves hands-on coding in Python and SQL to automate workflows, enhance pipeline efficiency, and manage operational tasks. While the majority of the work focuses on core data engineering responsibilities, there is also exposure to emerging tools like Microsoft Fabric and occasional work within Linux environments, contributing to a modern, evolving data platform.$110,000 to $126,000 - Exact compensation may vary based on several factors, including skills, experience, and education.We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com.To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/.
May 21, 2026
Albuquerque, NM
|
Materials Science & Engineering
|
Contract
|
$50 - $62 (hourly estimate)
{"JobID":533304,"JobType":["Contract"],"EmployerID":null,"Location":{"Latitude":-106.62,"Longitude":35.11,"Distance":null},"State":"New Mexico","Zip":"87106","ReferenceID":"RIC-48851979-c98c-405f-80af-77846c7a4fbc","PostedDate":"\/Date(1779406374000)\/","Description":"This Material Scientist role focuses on leading operational qualification and process optimization of carbothermal reduction and sintering furnaces within an R\u0026D environment. Responsibilities include guiding experiments, ensuring adherence to thermal profiles, analyzing material quality, troubleshooting process deviations, and documenting results to support continuous improvement and compliance. The position requires strong knowledge of thermal processing effects on material properties and proven ability to analyze process and quality data. Candidates should have experience in nuclear fuel R\u0026D or manufacturing, familiarity with equipment qualification and scale-up, and working knowledge of statistical process control and QA practices. A bachelor?s degree in Chemical, Materials, or Mechanical Engineering (advanced degree preferred), at least eight years of relevant experience, and strong organizational and communication skills are required. Salary ranges from 90K-130KWe are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com.To learn more about how we collect, keep, and process your private information, please review Insight Global\u0027s Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/.","Title":"Material Scientist (ET ? Sintering Development)","City":"Albuquerque","ExpirationDate":null,"PriorityOrder":0,"Requirements":"Leads qualification and optimization of new carbothermal reduction/sintering furnaces in R\u0026D. Guides technicians running experiments; ensures adherence to thermal profiles and process control.Performs characterization; analyzes quality/process data; troubleshoots deviations; documents results. Familiarity with equipment qualification protocols, scale-up considerations, SPC/QA. BS in ChemE/Materials/ME","Skills":"","Industry":"Materials Science \u0026 Engineering","Country":"US","Division":"IT","Office":null,"IsRemoteJob":false,"IsInternalJob":false,"ExtraValues":null,"__RecordIndex":0,"__OrdinalPosition":0,"__Timestamp":0,"Status":null,"ApplicantCount":0,"SubmittalCount":0,"ApplicationToHireRatio":0,"JobDuration":null,"SalaryHigh":62.0000,"SalaryLow":49.6000,"PayRateOvertime":0,"PayRateStraight":0,"Filled":0,"RemainingOpenings":0,"TotalOpenings":0,"Visa":null,"ClearanceType":null,"IsClearanceRequired":false,"IsHealthcare":false,"IsRemote":false,"EndClient":null,"JobCreatedDate":"\/Date(-62135578800000)\/","JobModifiedDate":"\/Date(-62135578800000)\/"}
This Material Scientist role focuses on leading operational qualification and process optimization of carbothermal reduction and sintering furnaces within an R&D environment. Responsibilities include... guiding experiments, ensuring adherence to thermal profiles, analyzing material quality, troubleshooting process deviations, and documenting results to support continuous improvement and compliance. The position requires strong knowledge of thermal processing effects on material properties and proven ability to analyze process and quality data. Candidates should have experience in nuclear fuel R&D or manufacturing, familiarity with equipment qualification and scale-up, and working knowledge of statistical process control and QA practices. A bachelor?s degree in Chemical, Materials, or Mechanical Engineering (advanced degree preferred), at least eight years of relevant experience, and strong organizational and communication skills are required. Salary ranges from 90K-130KWe are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com.To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/.
Apr 17, 2026
Raleigh, NC
|
Materials Science & Engineering
|
Contract
|
$59 - $74 (hourly estimate)
{"JobID":520174,"JobType":["Contract"],"EmployerID":null,"Location":{"Latitude":-78.65,"Longitude":35.82,"Distance":null},"State":"North Carolina","Zip":"27606","ReferenceID":"RAL-cc6eb4dc-a427-4ab9-9041-650a8065d402","PostedDate":"\/Date(1776438743000)\/","Description":"?Provide scientific and strategic input across various stages of clinical development to achieve market approval for new products and/or novel indications.?a. Duties performed as a member of a cross-functional team of internal and external experts and in support of the clinical director.?b. Projects are focused on medical devices, drugs, biologics, and/or other products for human use.?c. Projects may span from in-development to post-marketing studies and products.?Coordinate and integrate data and information from a variety of sources (e.g., internal and external studies, research documentation, and published literature) to support various clinical development initiatives.?Consolidate input from internal and external contributors to develop appropriate key messaging.?Support early-phase development activities, including curation, review, and interpretation of preclinical, exploratory data.?Provide scientific guidance and technical expertise within teams, across departments, and across functions by providing strategic, actionable direction, creating a strong sense of team unity and identity, and providing positive, constructive feedback.?Identify and troubleshoot study-specific issues, competing priorities, and clinical or scientific challenges.?Ensure effective, accurate, and timely communication of key issues and progress to the team and senior management.?Support planning and preparation for internal and external stakeholder meetings (e.g., workshops/summits, investigator meetings, scientific advisory boards, and regulatory meetings)?Write, review, edit, and approve high-quality and timely clinical documents, contributing scientific/technical expertise related to clinical development and document preparation.? Demonstrate understanding and interpretation of data generated from a variety of sources, including clinical study data and study results (i.e., tables, figures, and listings) and peer-reviewed literature and provide meaningful scientific interpretation and feedback to team members and other stakeholders.?Communicate with and work effectively and productively with multidisciplinary, international teams while executing project plans.We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com.To learn more about how we collect, keep, and process your private information, please review Insight Global\u0027s Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/.","Title":"Sr. Clinical Scientist","City":"Raleigh","ExpirationDate":null,"PriorityOrder":0,"Requirements":"?Masters Degree in Life Sciences ?Understanding of clinical product development, clinical trials, and global regulatory submissions?Knowledge of FDA and/or EMA regulations, GCP, ICH guidelines, and/or ISO 14155?Able to work on multiple projects simultaneously, while maintaining competing priorities, timelines, and quality of deliverables?Readily adaptable to changes in priorities?Demonstration of excellent verbal and written English, including understanding of English language usage in clinical/technical environments and standardized-writing styles.","Skills":"","Industry":"Materials Science \u0026 Engineering","Country":"US","Division":"IT","Office":null,"IsRemoteJob":false,"IsInternalJob":false,"ExtraValues":null,"__RecordIndex":0,"__OrdinalPosition":0,"__Timestamp":0,"Status":null,"ApplicantCount":0,"SubmittalCount":0,"ApplicationToHireRatio":0,"JobDuration":null,"SalaryHigh":74.0000,"SalaryLow":59.2000,"PayRateOvertime":0,"PayRateStraight":0,"Filled":0,"RemainingOpenings":0,"TotalOpenings":0,"Visa":null,"ClearanceType":null,"IsClearanceRequired":false,"IsHealthcare":false,"IsRemote":false,"EndClient":null,"JobCreatedDate":"\/Date(-62135578800000)\/","JobModifiedDate":"\/Date(-62135578800000)\/"}
?Provide scientific and strategic input across various stages of clinical development to achieve market approval for new products and/or novel indications.?a. Duties performed as a member of a... cross-functional team of internal and external experts and in support of the clinical director.?b. Projects are focused on medical devices, drugs, biologics, and/or other products for human use.?c. Projects may span from in-development to post-marketing studies and products.?Coordinate and integrate data and information from a variety of sources (e.g., internal and external studies, research documentation, and published literature) to support various clinical development initiatives.?Consolidate input from internal and external contributors to develop appropriate key messaging.?Support early-phase development activities, including curation, review, and interpretation of preclinical, exploratory data.?Provide scientific guidance and technical expertise within teams, across departments, and across functions by providing strategic, actionable direction, creating a strong sense of team unity and identity, and providing positive, constructive feedback.?Identify and troubleshoot study-specific issues, competing priorities, and clinical or scientific challenges.?Ensure effective, accurate, and timely communication of key issues and progress to the team and senior management.?Support planning and preparation for internal and external stakeholder meetings (e.g., workshops/summits, investigator meetings, scientific advisory boards, and regulatory meetings)?Write, review, edit, and approve high-quality and timely clinical documents, contributing scientific/technical expertise related to clinical development and document preparation.? Demonstrate understanding and interpretation of data generated from a variety of sources, including clinical study data and study results (i.e., tables, figures, and listings) and peer-reviewed literature and provide meaningful scientific interpretation and feedback to team members and other stakeholders.?Communicate with and work effectively and productively with multidisciplinary, international teams while executing project plans.We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com.To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/.
Dec 10, 2025
East Greenbush, NY
|
Project Manager
|
Contract
|
$43 - $54 (hourly estimate)
{"JobID":475079,"JobType":["Contract"],"EmployerID":null,"Location":{"Latitude":-73.73,"Longitude":42.64,"Distance":null},"State":"New York","Zip":"12144","ReferenceID":"NYC-6fc34230-55aa-44bb-9a6d-0f59cb885790","PostedDate":"\/Date(1765395844000)\/","Description":"Insight Global\u0027s client in Albany NY, is seeking a Data Entry candidate to help lead the SoftMax project and manage the team of system coordinators and system administrators. Their time will be mostly spent sitting in on meetings with the scientist across the lab space, working with the IT team and translating deliverables into action items for present to the business. This individual will also be responsible for managing validation support, technical writing, dashboards, data integrity, compliance, audit trail reviews and coordination of the company\u0027s systems. This person should come from a business analyst background and have experience managing teams in fast paced environments to be able to successfully provide project support. In addition, clear communication is needed since this person will be working cross functionally to report project timelines to represent the IT labs space. This person should be a self-starter and highly resourceful due to the volume of work.We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com.To learn more about how we collect, keep, and process your private information, please review Insight Global\u0027s Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/.","Title":"Data Entry","City":"East Greenbush","ExpirationDate":null,"PriorityOrder":0,"Requirements":"5+ years working in Data EntryPrevious management experience within a healthcare, education, software or engineering spaceExperience leading system upgradesFamiliarity with business analyst tolls ? Microsoft and PowerPointBachelor?s Degree","Skills":"","Industry":"Project Manager","Country":"US","Division":"IT","Office":null,"IsRemoteJob":false,"IsInternalJob":false,"ExtraValues":null,"__RecordIndex":0,"__OrdinalPosition":0,"__Timestamp":0,"Status":null,"ApplicantCount":0,"SubmittalCount":0,"ApplicationToHireRatio":0,"JobDuration":null,"SalaryHigh":54.0000,"SalaryLow":43.2000,"PayRateOvertime":0,"PayRateStraight":0,"Filled":0,"RemainingOpenings":0,"TotalOpenings":0,"Visa":null,"ClearanceType":null,"IsClearanceRequired":false,"IsHealthcare":false,"IsRemote":false,"EndClient":null,"JobCreatedDate":"\/Date(-62135578800000)\/","JobModifiedDate":"\/Date(-62135578800000)\/"}
Insight Global's client in Albany NY, is seeking a Data Entry candidate to help lead the SoftMax project and manage the team of system coordinators and system administrators. Their time will be... mostly spent sitting in on meetings with the scientist across the lab space, working with the IT team and translating deliverables into action items for present to the business. This individual will also be responsible for managing validation support, technical writing, dashboards, data integrity, compliance, audit trail reviews and coordination of the company's systems. This person should come from a business analyst background and have experience managing teams in fast paced environments to be able to successfully provide project support. In addition, clear communication is needed since this person will be working cross functionally to report project timelines to represent the IT labs space. This person should be a self-starter and highly resourceful due to the volume of work.We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com.To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/.