Job Search Results for Pharmaceutical
Mar 18, 2026
Lower Gwynedd, PA
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Laboratory Technician
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Contract
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$34 - $43 (hourly estimate)
{"JobID":507877,"JobType":["Contract"],"EmployerID":null,"Location":{"Latitude":-75.22,"Longitude":40.15,"Distance":null},"State":"Pennsylvania","Zip":"19002","ReferenceID":"PHL-643af4f6-2b66-4956-ad6d-9126682f45ba","PostedDate":"\/Date(1773800373000)\/","Description":"Our large pharmaceutical client in Spring House, PA is seeking an Associate Scientist to join their growing Cell Therapy Drug Product Development organization and support ongoing CAR-T programs. Training is provided for this role and this team provides a lot of opportunity for growth! Primary responsibilities include:-Support CAR-T formulation and cryopreservation activities in BSL2+ labs-Formulation execution across various studies-Collect, verify and analyze data and results-Participate in data analysis of process characterization studies-Review, understand, and follow protocols and SOPs -Implement and maintain high quality standards for all aspects of work conducted including adherence to regulatory GLP/GMP, departmental, and safety \u0026 compliance guidelines-Track and coordinate inventory and manage sample coordination, hand-off, and storage across other internal teamsWe 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":"Associate Scientist","City":"Lower Gwynedd","ExpirationDate":null,"PriorityOrder":0,"Requirements":"-1+ year of experience with cell culture and aseptic techniques-Cell cryopreservation experience including formulation, freezing, and transfer to storage -Bachelor\u0027s Degree or above in Biology, Biochemistry or related discipline -Strong organization, communication and problem-solving skills. Comfortable with communicating and coordinating cross functionally with multiple teams.","Skills":"-CAR T Cell Therapy experience Preferred-Experience with Liquid Nitrogen Freezer (LN2)-Cell selection equipment such as Xuri, Sefia or Prodigy-Cell washing equipment such as Lovo, Cue or Prodigy-Experience using cell counter, NC200 or XM30-Flow cytometry -Experience in a GMP lab setting","Industry":"Laboratory Technician","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":43.0000,"SalaryLow":34.4000,"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)\/"}
Our large pharmaceutical client in Spring House, PA is seeking an Associate Scientist to join their growing Cell Therapy Drug Product Development organization and support ongoing CAR-T programs.... Training is provided for this role and this team provides a lot of opportunity for growth! Primary responsibilities include:-Support CAR-T formulation and cryopreservation activities in BSL2+ labs-Formulation execution across various studies-Collect, verify and analyze data and results-Participate in data analysis of process characterization studies-Review, understand, and follow protocols and SOPs -Implement and maintain high quality standards for all aspects of work conducted including adherence to regulatory GLP/GMP, departmental, and safety & compliance guidelines-Track and coordinate inventory and manage sample coordination, hand-off, and storage across other internal teamsWe 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/.
Mar 24, 2026
Upper Providence, PA
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Engineering (Non IT)
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Contract
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$38 - $48 (hourly estimate)
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One of our large pharmaceutical clients is actively hiring a Hepatology Scientist to join their R&D Team. Primary goal of this project is to develop robust and reproducible human primary... cell-derived complex in vitro model for steatotic liver disease demonstrating the fibrotic and inflammatory response to steatotic liver disease stimuli.We are seeking a PhD-level scientist to support experimental research within the Hepatology team, with a primary focus on macrophage biology and co-culture model development. The successful candidate will design and execute laboratory experiments to progress a macrophage?fibroblast co-culture system, contributing to ongoing liver fibrosis modeling initiatives.This role involves hands-on laboratory work, experimental design, data analysis, and close collaboration with internal scientific stakeholders.-Design, develop, and execute macrophage-based co-culture assays to support liver fibrosis modeling-Perform in-vitro experiments involving macrophages and fibroblasts, including co-culture system optimization-Generate proof-of-concept data demonstrating fibrotic macrophage activation of liver fibroblasts-Utilize flow cytometry and imaging techniques to characterize immune cell populations and cellular responses-Analyze, interpret, and document experimental data to inform model development and decision-making-Collaborate with hepatology and disease area scientists to align experimental outcomes with project objectives-Contribute to experimental planning, troubleshooting, and continuous improvement of assay workflowsWe 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 14, 2026
Clayton, NC
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Engineering (Non IT)
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Contract
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$48 - $60 (hourly estimate)
{"JobID":518801,"JobType":["Contract"],"EmployerID":null,"Location":{"Latitude":-78.45,"Longitude":35.64,"Distance":null},"State":"North Carolina","Zip":"27520","ReferenceID":"RAL-9afff886-8153-4d32-a833-99c2707e6f57","PostedDate":"\/Date(1776197732000)\/","Description":"Insight Global is seeking an IT Automation Engineer for a pharmaceutical client in the Raleigh area. The IT Automation Engineer will support the Fill Finish Expansion Project at their greenfield facility. These engineers will support the deployment, integration, testing, and troubleshooting of automated assembly and packaging equipment within Finished Products buildings. The role is hands-on and project-focused, supporting OEM equipment, PLC/SCADA systems, MES, serialization, and IT/OT integration in a highly regulated GMP environment.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":"IT Automation Engineer","City":"Clayton","ExpirationDate":null,"PriorityOrder":0,"Requirements":"Strong hands-on experience supporting automation systems in manufacturingExperience working with OEM packaging and assembly equipmentPLC experience with one or more of the following:Schneider, B\u0026R, Allen-Bradley ControlLogix, SiemensExperience with SCADA systems (FactoryTalk preferred)Familiarity with MES (PAS-X) and serialization systems (Uhlmann Track \u0026 Trace)Experience executing SAT / IV / OV testingUnderstanding of IT/OT integration in industrial environmentsExperience working in regulated industries (pharma, biotech, medical device preferred)","Skills":"Experience with SQL Server, Aveva PI,Vision system experience Networking fundamentals in industrial environmentsCybersecurity awareness specific to OT systemsGreenfield or large CAPEX project experience","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":60.0000,"SalaryLow":48.0000,"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)\/"}
Insight Global is seeking an IT Automation Engineer for a pharmaceutical client in the Raleigh area. The IT Automation Engineer will support the Fill Finish Expansion Project at their greenfield... facility. These engineers will support the deployment, integration, testing, and troubleshooting of automated assembly and packaging equipment within Finished Products buildings. The role is hands-on and project-focused, supporting OEM equipment, PLC/SCADA systems, MES, serialization, and IT/OT integration in a highly regulated GMP environment.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/.
Feb 06, 2026
Lower Gwynedd, PA
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Engineering (Non IT)
|
Contract
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$54 - $68 (hourly estimate)
{"JobID":491834,"JobType":["Contract"],"EmployerID":null,"Location":{"Latitude":-75.22,"Longitude":40.18,"Distance":null},"State":"Pennsylvania","Zip":"19477","ReferenceID":"PHL-71f904cc-4936-4281-aca3-00c395267828","PostedDate":"\/Date(1770409022000)\/","Description":"One of our large pharmaceutical clients is hiring for a Sr. QA Validation Specialist to join their team in Spring House, PA. This individual will support the Advanced Therapy division. Responsibilities will include: -Provide overall Quality Validation support of the new Advanced Therapy Facility inclusive of manufacturing and in process testing laboratory. Oversee and perform quality approval of Analytical Instrument Qualification (AIQ) and Risk Based C\u0026Q activities following procedures. Performing Equipment Releases for equipment and instruments per local procedures. -Will perform the following duties but not limited to: Review and Approval of CMMS Change Controls, Work Order Cancelation/Deferment Forms and Validation Forms. -Work on a team for quality responsible for instruments undergoing AIQ, C\u0026Q, and review and approve associated documentation. Complete equipment/instrument lifecycle management forms. -Complete required release paperwork. Perform quality review/approval of assessments, protocols, final reports, and standard operating procedures as required. -All activities will be executed under the direction Quality Validation personnel.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. QA Validation Specialist","City":"Lower Gwynedd","ExpirationDate":null,"PriorityOrder":0,"Requirements":"-Minimum 3 years of experience within Computer System Validation (CSV) or quality oversight of CSV -Minimum 5 years of total pharmacuteical GMP working experience with data integrity -Previous hands-on Delta V Experience -Knowledge and exposure with 21 Part 11 Compliance and Annex 11 Compliance- Knowledge of Equipment Lifecycle Management Process-Validation/Qualification of GxP Lab Equipment and Process Equipment-Experience with Change Management Process-Experience navigating and recording documentation in electronic systems per Good Documentation Practices","Skills":"-Document Management Systems- Change Control sytems (such as TrackWise/Salesforce)-SAP-EMS, BMS, Green Button Go","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":68.0000,"SalaryLow":54.4000,"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)\/"}
One of our large pharmaceutical clients is hiring for a Sr. QA Validation Specialist to join their team in Spring House, PA. This individual will support the Advanced Therapy division.... Responsibilities will include: -Provide overall Quality Validation support of the new Advanced Therapy Facility inclusive of manufacturing and in process testing laboratory. Oversee and perform quality approval of Analytical Instrument Qualification (AIQ) and Risk Based C&Q activities following procedures. Performing Equipment Releases for equipment and instruments per local procedures. -Will perform the following duties but not limited to: Review and Approval of CMMS Change Controls, Work Order Cancelation/Deferment Forms and Validation Forms. -Work on a team for quality responsible for instruments undergoing AIQ, C&Q, and review and approve associated documentation. Complete equipment/instrument lifecycle management forms. -Complete required release paperwork. Perform quality review/approval of assessments, protocols, final reports, and standard operating procedures as required. -All activities will be executed under the direction Quality Validation personnel.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/.
Mar 30, 2026
Lower Gwynedd, PA
|
Laboratory Technician
|
Contract
|
$43 - $54 (hourly estimate)
{"JobID":512807,"JobType":["Contract"],"EmployerID":null,"Location":{"Latitude":-75.22,"Longitude":40.15,"Distance":null},"State":"Pennsylvania","Zip":"19002","ReferenceID":"PHL-7986f8cb-8179-49c6-94c8-532bbfbfa4b5","PostedDate":"\/Date(1774904469000)\/","Description":"Our large pharmaceutical client in Spring House, PA is seeking a Scientist to join the High-Throughput Screening (HTP) team to support protein release quality control (QC) and DNA handling activities. The primary function is protein QC specifically to measure concentration and endotoxins to determine whether there is contamination and if the protein meets quality standards required to be used in critical experiments. Key Responsibilities:-Perform protein release QC activities in a high-throughput environment-Handle and process DNA samples in accordance with established protocols-Mammalian cell culture-Support HTP workflows, ensuring accuracy, consistency, and data integrity-Work independently to execute assigned workflows and experiments-Document experimental results and follow QC and laboratory best practices-Collaborate with cross-functional team members as needed to support project goalsWe 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":"Protein QC Scientist","City":"Lower Gwynedd","ExpirationDate":null,"PriorityOrder":0,"Requirements":"-Bachelor\u0027s of Master\u0027s Degree with 2?5 years of industry experience in a laboratory setting-PhD in a biology-related field with 1?3 years of hands-on industry experience-Direct experience with mammalian cell culture (2+ years preferred)-HPLC-Molecular Biology experience-Strong understanding of protein QC and DNA handling techniques-Ability to work independently in a fast-paced, high-throughput environment","Skills":"-Experience with laboratory automation - Liquid handlers such as Tecan or Hamilton-Background working within high-throughput screening (HTP) teams","Industry":"Laboratory Technician","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":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)\/"}
Our large pharmaceutical client in Spring House, PA is seeking a Scientist to join the High-Throughput Screening (HTP) team to support protein release quality control (QC) and DNA handling... activities. The primary function is protein QC specifically to measure concentration and endotoxins to determine whether there is contamination and if the protein meets quality standards required to be used in critical experiments. Key Responsibilities:-Perform protein release QC activities in a high-throughput environment-Handle and process DNA samples in accordance with established protocols-Mammalian cell culture-Support HTP workflows, ensuring accuracy, consistency, and data integrity-Work independently to execute assigned workflows and experiments-Document experimental results and follow QC and laboratory best practices-Collaborate with cross-functional team members as needed to support project goalsWe 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/.
Mar 18, 2026
Lower Gwynedd, PA
|
Project Manager
|
Contract
|
$70 - $87 (hourly estimate)
{"JobID":507878,"JobType":["Contract"],"EmployerID":null,"Location":{"Latitude":-75.22,"Longitude":40.15,"Distance":null},"State":"Pennsylvania","Zip":"19002","ReferenceID":"PHL-be3190ea-b158-4018-bd6f-47a0ee8239ff","PostedDate":"\/Date(1773800181000)\/","Description":"Our large pharmaceutical client in Spring House, PA is seeking an experienced Project Manager to lead a multi-stakeholder lab automation initiative within the Large Molecule Discovery group in R\u0026D. The objective of this initiative is to automate core functions including protein production, cell culture, functional assays, biophysics analysis, and the sample management inventory system. This role will coordinate diverse functional teams with varying technical needs and timelines, and manage collaboration across internal IT, safety and Operations teams, as well as multiple external vendors.Core responsibilities:?Develop and maintain integrated project plans, timelines, and milestones for the lab automation program?Facilitate communication and alignment across scientific, operational, and technology stakeholders?Oversee vendor management, ensuring deliverables meet technical and operational requirements?Manage risks and dependencies across functional groups?Provide regular status updates and ensure issues are addressed promptly?Organize and manage team meetingsWe 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":"Project Manager","City":"Lower Gwynedd","ExpirationDate":null,"PriorityOrder":0,"Requirements":"-Bachelor?s degree in a relevant field (e.g. Life Sciences, Computer Sciences, Engineering, Business) -3+ years of relevant experience as a Project Manager in the life sciences industry-Proven experience managing complex, cross-functional technical projects in a research or laboratory environment -Strong stakeholder management skills with ability to balance competing priorities","Skills":"-Familiarity with lab automation technologies and workflows - ideally liquid handlers such as Tecan-Project management credentials such as PMP, PRINCE2, Waterfall or Agile certifications","Industry":"Project Manager","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":87.0000,"SalaryLow":69.6000,"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)\/"}
Our large pharmaceutical client in Spring House, PA is seeking an experienced Project Manager to lead a multi-stakeholder lab automation initiative within the Large Molecule Discovery group in R&D. ... The objective of this initiative is to automate core functions including protein production, cell culture, functional assays, biophysics analysis, and the sample management inventory system. This role will coordinate diverse functional teams with varying technical needs and timelines, and manage collaboration across internal IT, safety and Operations teams, as well as multiple external vendors.Core responsibilities:?Develop and maintain integrated project plans, timelines, and milestones for the lab automation program?Facilitate communication and alignment across scientific, operational, and technology stakeholders?Oversee vendor management, ensuring deliverables meet technical and operational requirements?Manage risks and dependencies across functional groups?Provide regular status updates and ensure issues are addressed promptly?Organize and manage team meetingsWe 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 08, 2026
Boston, MA
|
Security Engineering
|
Contract
|
$50 - $62 (hourly estimate)
{"JobID":516833,"JobType":["Contract"],"EmployerID":null,"Location":{"Latitude":-71.0418,"Longitude":42.3466,"Distance":null},"State":"Massachusetts","Zip":"02210","ReferenceID":"BOS-120da826-5a2e-441c-bc9b-ffd273aa0cf0","PostedDate":"\/Date(1775685149000)\/","Description":"A pharmaceutical company based out of Boston is seeking a hands-on Cybersecurity Engineer supporting day-to-day security operations within a regulated enterprise environment. This role joins an existing team of 4 and is focused on execution, helping relieve workload so senior engineers can focus on complex initiatives.The engineer will partner closely with the CSOC to investigate, triage, and remediate endpoint-related incidents, with a heavy emphasis on DLP (?50% of workload) and the remainder across endpoint security, incident response, and vulnerability management.This is not a strategy or leadership role ? success is measured by responsiveness, accuracy, and ability to independently close tickets and execute remediation.?Workload: ~50% DLP / ~50% other security operations?Tools in use: CrowdStrike, Microsoft Intune, Forcepoint (possible future move to Proofpoint)$70/hrWe 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":"Incident Response / Cyber Security Engineer","City":"Boston","ExpirationDate":null,"PriorityOrder":0,"Requirements":"?5 years of hands-on experience in cybersecurity operations or SOC environments?Prior SOC experience ?Strong, hands-on experience with: oCrowdStrike (EDR/XDR)oMicrosoft IntuneoDLP tools (Forcepoint preferred; Proofpoint or other DLP acceptable)oVulnerability management tools (Tenable or equivalent)?Proven experience: oResponding to day-to-day security incidentsoClosing security tickets independentlyoImplementing mitigation and containment actions?Experience working in a regulated / compliance-driven environment oGxP exposure required (training or prior hands-on experience)","Skills":"?Embedded or closely partnered CSOC experience?Threat hunting or proactive detection exposure?Audit or regulatory assessment support?Security certifications (Security+, GSEC, GCED, GCIA)","Industry":"Security 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)\/"}
A pharmaceutical company based out of Boston is seeking a hands-on Cybersecurity Engineer supporting day-to-day security operations within a regulated enterprise environment. This role joins an... existing team of 4 and is focused on execution, helping relieve workload so senior engineers can focus on complex initiatives.The engineer will partner closely with the CSOC to investigate, triage, and remediate endpoint-related incidents, with a heavy emphasis on DLP (?50% of workload) and the remainder across endpoint security, incident response, and vulnerability management.This is not a strategy or leadership role ? success is measured by responsiveness, accuracy, and ability to independently close tickets and execute remediation.?Workload: ~50% DLP / ~50% other security operations?Tools in use: CrowdStrike, Microsoft Intune, Forcepoint (possible future move to Proofpoint)$70/hrWe 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/.
Mar 10, 2026
Parsippany, NJ
|
Engineering (Non IT)
|
Contract
|
$50 - $62 (hourly estimate)
{"JobID":504617,"JobType":["Contract"],"EmployerID":null,"Location":{"Latitude":-74.4061,"Longitude":40.862,"Distance":null},"State":"New Jersey","Zip":"07054","ReferenceID":"NNJ-02b6a38a-cda8-4591-a2da-ccbc81684b99","PostedDate":"\/Date(1773153089000)\/","Description":"Seeking a mid- to senior-level Validation Engineer to support commissioning and qualification activities within a pharmaceutical manufacturing environment. The role will be responsible for generating and executing IQ, OQ, and PQ protocols for equipment, utilities, and packaging systems, ensuring compliance with cGMP and regulatory expectations. The candidate should be comfortable working both independently and collaboratively, with the ability to lead validation activities and drive projects to completion.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":"Senior Validation Engineer","City":"Parsippany","ExpirationDate":null,"PriorityOrder":0,"Requirements":"? Author and execute Commissioning, Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) protocols.? Support qualification of process equipment, packaging lines, laboratory equipment, utilities, and facility systems.? Perform temperature mapping studies for controlled temperature equipment and storage areas.? Support cleanroom and room qualification activities.? Execute or support media fills (aseptic process simulations) and smoke studies.? Support Environmental Monitoring (EM) studies.? Investigate and document deviations encountered during qualification activities.? Prepare validation documentation and summary reports.Work cross-functionally with internal teams (i.e., Engineering, Quality, Manufacturing, Supply Chain, and Validation) to support qualification activities and ensure project timelines are met.","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":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)\/"}
Seeking a mid- to senior-level Validation Engineer to support commissioning and qualification activities within a pharmaceutical manufacturing environment. The role will be responsible for generating... and executing IQ, OQ, and PQ protocols for equipment, utilities, and packaging systems, ensuring compliance with cGMP and regulatory expectations. The candidate should be comfortable working both independently and collaboratively, with the ability to lead validation activities and drive projects to completion.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 15, 2026
East Greenbush, NY
|
Chemical Engineering
|
Contract
|
$59 - $74 (hourly estimate)
{"JobID":519468,"JobType":["Contract"],"EmployerID":null,"Location":{"Latitude":-73.73,"Longitude":42.64,"Distance":null},"State":"New York","Zip":"12144","ReferenceID":"NYC-33725bcf-b6c9-4357-aa63-e9a26d0632ea","PostedDate":"\/Date(1776291011000)\/","Description":"Insight Global is seeking a QA to join one of our largest pharmaceutical clients 5x/week onsite in Rensselaer, NY. This individual will be joining the Cleanroom team within the Facilities Engineering space assisting in lifecycle of reports being processed by the QA team. They will be responsible for managing reports from vendors, executing report reviews, adjusting QA comments, and pushing through to the next step in the report lifecycle. They will be expected to perform a high-level review through QA, identify any Gx issues, and ensuring acceptance criteria is accurate. This will be a mainly individual contributor but will be expected to work cross functionally with QA for oversight from the team when needed.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":"QA","City":"East Greenbush","ExpirationDate":null,"PriorityOrder":0,"Requirements":"-4-5 years of experience -GxP/heavy documentation experience -Strong communication skills and able to work cross functionally -Background in Pharma or life scienes -Detail oriented","Skills":"N/A","Industry":"Chemical 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)\/"}
Insight Global is seeking a QA to join one of our largest pharmaceutical clients 5x/week onsite in Rensselaer, NY. This individual will be joining the Cleanroom team within the Facilities Engineering... space assisting in lifecycle of reports being processed by the QA team. They will be responsible for managing reports from vendors, executing report reviews, adjusting QA comments, and pushing through to the next step in the report lifecycle. They will be expected to perform a high-level review through QA, identify any Gx issues, and ensuring acceptance criteria is accurate. This will be a mainly individual contributor but will be expected to work cross functionally with QA for oversight from the team when needed.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/.
Nov 05, 2025
Easthampton Town, MA
|
Mechanical Assembler
|
Perm
|
$18 - $25 (hourly estimate)
{"JobID":464038,"JobType":["Perm"],"EmployerID":null,"Location":{"Latitude":-72.7177,"Longitude":42.2914,"Distance":null},"State":"Massachusetts","Zip":"01027","ReferenceID":"DGO-529d7395-bbeb-46e7-87cb-749db6af0f56","PostedDate":"\/Date(1762368976000)\/","Description":"Insight Global is seeking 2 Cleanroom Assembly Technicians for our client, a key partner in the pharmaceutical sector, based in Easthampton, MA. These Assembly Technicians will be responsible for performing manual labor in a cleanroom production line; assembling parts ranging from individual pieces, single molded assemblies to complete kits.DUTIES AND RESPONSIBILITIES:?Works as part of a production team to assemble parts.?Sorts and places material or items on tables, racks or bins.?Assembles parts manually or with machinery?Uses production machinery to seal final products per SOPs?Uses testing equipment to qualify (pass or fail) assembled parts.?Cleans assembled parts and places in protective bags.?Removes extraneous material from molded parts as necessary.?Uses small tools or machines to manipulate parts for assembly.?Cleans and glues parts per SOPs?Performs other related duties as assigned by management.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":"Cleanroom Assembly Technician","City":"Easthampton Town","ExpirationDate":null,"PriorityOrder":0,"Requirements":"High school diploma or general education degree (GED); 3 months related experience and/or training; or equivalent combination of education and experience.Must be detail-oriented and work effectively under pressure while meeting all applicable deadlines.Frequently required to lift/push/carry items up to 25 poundsDue to particulate requirements of being in a cleanroom this position is a non-smoking position.","Skills":"","Industry":"Mechanical Assembler","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":25.0000,"SalaryLow":18.0000,"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)\/"}
Insight Global is seeking 2 Cleanroom Assembly Technicians for our client, a key partner in the pharmaceutical sector, based in Easthampton, MA. These Assembly Technicians will be responsible for... performing manual labor in a cleanroom production line; assembling parts ranging from individual pieces, single molded assemblies to complete kits.DUTIES AND RESPONSIBILITIES:?Works as part of a production team to assemble parts.?Sorts and places material or items on tables, racks or bins.?Assembles parts manually or with machinery?Uses production machinery to seal final products per SOPs?Uses testing equipment to qualify (pass or fail) assembled parts.?Cleans assembled parts and places in protective bags.?Removes extraneous material from molded parts as necessary.?Uses small tools or machines to manipulate parts for assembly.?Cleans and glues parts per SOPs?Performs other related duties as assigned by management.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/.