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Apr 29, 2026

New Haven, CT

|

Laboratory Technician

|

Contract

|

$20 - $25 (hourly estimate)

{"JobID":524554,"JobType":["Contract"],"EmployerID":null,"Location":{"Latitude":-72.9383,"Longitude":41.3255,"Distance":null},"State":"Connecticut","Zip":"06511","ReferenceID":"HNJ-6035674d-b515-48e4-9e23-408e1fbdf15d","PostedDate":"\/Date(1777477196000)\/","Description":"A world-renowned pharmaceutical company is looking for a strong Clinical Documentation Specialist to support the lab in New Haven, CT. This person will be responsible for formatting, transfers, and archives both clinical biomarker test results and study documents in support of Pfizer clinical trials documentationWe 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":"Clinical Documentation Specialist","City":"New Haven","ExpirationDate":null,"PriorityOrder":0,"Requirements":"2-4 years work experience in biotechnology or pharmaceutical industry with demonstrated ability in the management of document information and workflowsWork experience in a regulated lab or quality assurance department preferredknowledgeable of good documentation practicesAdvanced proficiency in Microsoft Excel, Word, and TeamsTransfer signed study documents to long-term archival and link to trial master files when appropriateCommunicate openly with internal Biomarker Lab Head and Project Leads and with external Biomarker Clinical Assay Leads and master file ownersAll deliverables adhere to agreed upon timelinesAttend biweekly Biomarker Study Management Meetings and monthly Clinical Bioanalytic Meetings Positive attitude with a desire to learn and contribute to large team projects that occasionally require flexible working hours","Skills":"","Industry":"Laboratory Technician","Country":"US","Division":"IGH","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":20.0000,"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 world-renowned pharmaceutical company is looking for a strong Clinical Documentation Specialist to support the lab in New Haven, CT. This person will be responsible for formatting, transfers, and... archives both clinical biomarker test results and study documents in support of Pfizer clinical trials documentationWe 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

New York, NY

|

Engineering (Non IT)

|

Perm

|

$85k - $150k (estimate)

{"JobID":510665,"JobType":["Perm"],"EmployerID":null,"Location":{"Latitude":-73.99,"Longitude":40.71,"Distance":null},"State":"New York","Zip":"10018","ReferenceID":"OCC-87c16dcb-36b4-4cb9-bdb4-e0e85a200b7d","PostedDate":"\/Date(1774392485000)\/","Description":"Insight Global is seeking a Energy Engineer to support a leading energy engineering firm delivering energy efficiency, building performance, and controls-focused projects across the greater New York City area. This role works onsite with clients?including pharmaceutical facilities, hospitals, and higher-education campuses?to identify, develop, and implement energy conservation measures from concept through execution.The Energy Engineer will spend the majority of time onsite conducting field investigations, testing equipment, analyzing BAS/BMS trends, and gathering data to support energy analysis and project development. Over long-term onsite engagements, this individual will proactively identify opportunities, develop implementation roadmaps, and collaborate directly with client stakeholders, project managers, and subcontractors to deliver high-value solutions with minimal oversight.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":"Energy Engineer","City":"New York","ExpirationDate":null,"PriorityOrder":0,"Requirements":"? 3+ years of experience as an Energy Engineer? Strong technical fundamentals in energy analysis and building systems? Experience with energy audits and/or retro-commissioning? Hands-on experience with BAS/BMS, including trend analysis? Experience working onsite in pharmaceutical, hospital, or higher-education environments is preferred? Strong communication, organization, and time-management skills? Proficiency in Microsoft Office (Excel required)","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":150000.0000,"SalaryLow":85000.0000,"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 a Energy Engineer to support a leading energy engineering firm delivering energy efficiency, building performance, and controls-focused projects across the greater New York... City area. This role works onsite with clients?including pharmaceutical facilities, hospitals, and higher-education campuses?to identify, develop, and implement energy conservation measures from concept through execution.The Energy Engineer will spend the majority of time onsite conducting field investigations, testing equipment, analyzing BAS/BMS trends, and gathering data to support energy analysis and project development. Over long-term onsite engagements, this individual will proactively identify opportunities, develop implementation roadmaps, and collaborate directly with client stakeholders, project managers, and subcontractors to deliver high-value solutions with minimal oversight.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 03, 2026

Parsippany, NJ

|

Sterile Processing Technician

|

Contract-to-perm

|

$22 - $27 (hourly estimate)

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Insight Global is seeking a Production Operator to support aseptic manufacturing operations on a permanent 3rd shift schedule (11:00 PM ? 7:15 AM, Monday?Saturday). This individual will work in a... controlled cleanroom environment, contributing to fill/finish operations and supporting the setup, operation, and basic troubleshooting of equipment within classified production areas (A/B, C, D).Responsibilities include operating and maintaining equipment such as the stopper processor, vial washer, tunnel, capper, filler, autoclaves, VHP pass-thru, small parts washer/dryer, and lyophilizer. The role also involves identifying and resolving minor mechanical issues to ensure consistent production performance.The ideal candidate will uphold strict adherence to GMP and aseptic processing standards while maintaining a strong focus on quality and compliance. This is an excellent opportunity for individuals looking to build a long-term career in pharmaceutical manufacturing and gain hands-on experience in aseptic operations.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 30, 2026

Syracuse, NY

|

Engineering (Non IT)

|

Contract

|

$56 - $70 (hourly estimate)

{"JobID":524966,"JobType":["Contract"],"EmployerID":null,"Location":{"Latitude":-76.14,"Longitude":43.04,"Distance":null},"State":"New York","Zip":"13202","ReferenceID":"RIC-1ebbb5d8-5252-4ef9-8c69-37acd3233256","PostedDate":"\/Date(1777554665000)\/","Description":"Insight Global is seeking a Construction Manager to join our client\u0027s Advanced Manufacturing Team. This role will drive successful delivery of complex, mission-critical, and industrial construction projects across the United States. You would be responsible to lead field execution, manage subcontractor performance, uphold safety standards, and ensure projects are delivered on time, within scope, and on budget.?This project is a renovation of a clean room for a pharmaceutical client. Our client will be renovating and reorienting the space as well as installing four high-volume stainless-steel vessels that will be pipelined to the manufacturing suites. They would like someone who understands all the disciplines/MEPs.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":"Construction Manager - Pharmaceuticals","City":"Syracuse","ExpirationDate":null,"PriorityOrder":0,"Requirements":"- Bachelor\u0027s degree in construction management, civil/mechanical/electrical engineering, or a related field. - 5 years minimum experience within construction management on industrial, pharmaceutical, or manufacturing projects. - Working knowledge of Microsoft Office Suite as well as scheduling and construction management software. They will be using ACC (Autodesk Construction Cloud).","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":70.0000,"SalaryLow":56.0000,"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 a Construction Manager to join our client's Advanced Manufacturing Team. This role will drive successful delivery of complex, mission-critical, and industrial construction... projects across the United States. You would be responsible to lead field execution, manage subcontractor performance, uphold safety standards, and ensure projects are delivered on time, within scope, and on budget.?This project is a renovation of a clean room for a pharmaceutical client. Our client will be renovating and reorienting the space as well as installing four high-volume stainless-steel vessels that will be pipelined to the manufacturing suites. They would like someone who understands all the disciplines/MEPs.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 01, 2026

East Whiteland, PA

|

Laboratory Technician

|

Contract

|

$38 - $47 (hourly estimate)

{"JobID":525647,"JobType":["Contract"],"EmployerID":null,"Location":{"Latitude":-75.51,"Longitude":40.03,"Distance":null},"State":"Pennsylvania","Zip":"19355","ReferenceID":"PHL-c3b021b4-b149-4533-b325-a185325b6071","PostedDate":"\/Date(1777663227000)\/","Description":"Our large pharmaceutical client in Malvern, PA is looking for a Lab Equipment Systems Specialist to support the implementation of a new equipment management system. This induvial will transition lab equipment from one program to another while maintaining contracts and PM timelines of established and new equipment as to not disrupt testing and delay timelines. Roles \u0026 Responsibilities:?Champion transition to new systemoLearn and train others on new systemoTransfer equipment information from Maximo to SAPoManage new system?Build new Spotfire Dashboard to monitor and log equipment activities?Maintain current and new equipment oWork within Maximo system for scheduling and work order activities until new system is fully establishedoSchedule and host vendor visits for repairs and calibration activityoCommunicate with team on instrument related itemsoObtain quotes and purchase vendor contracts on equipmentoAssist with onboarding of new assets and decommissioning of retired systemsoMaking new logbooks/updating logbooksWe 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":"Laboratory Equipment Systems Specialist","City":"East Whiteland","ExpirationDate":null,"PriorityOrder":0,"Requirements":"?2+ years of experience as a Lab System Specialist in the pharmaceutical industry?Vendor management experience?Excellent communications skills ?Excellent time management and organizational skills ?Track record of being able to multi-task","Skills":"?Previous inventory management experience (Maximo would be an example)?Familiarity with BIOVIA or LIMs software","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":47.0000,"SalaryLow":37.6000,"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 Malvern, PA is looking for a Lab Equipment Systems Specialist to support the implementation of a new equipment management system. This induvial will transition lab... equipment from one program to another while maintaining contracts and PM timelines of established and new equipment as to not disrupt testing and delay timelines. Roles & Responsibilities:?Champion transition to new systemoLearn and train others on new systemoTransfer equipment information from Maximo to SAPoManage new system?Build new Spotfire Dashboard to monitor and log equipment activities?Maintain current and new equipment oWork within Maximo system for scheduling and work order activities until new system is fully establishedoSchedule and host vendor visits for repairs and calibration activityoCommunicate with team on instrument related itemsoObtain quotes and purchase vendor contracts on equipmentoAssist with onboarding of new assets and decommissioning of retired systemsoMaking new logbooks/updating logbooksWe 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 23, 2026

Andover, MA

|

Engineering (Non IT)

|

Contract

|

$36 - $45 (hourly estimate)

{"JobID":509487,"JobType":["Contract"],"EmployerID":null,"Location":{"Latitude":-71.1615,"Longitude":42.6484,"Distance":null},"State":"Massachusetts","Zip":"01810","ReferenceID":"RAL-f84b26d8-8249-4b4a-ad24-3c17745ed66b","PostedDate":"\/Date(1774268430000)\/","Description":"We are looking for a Downstream Scientist to support our pharmaceutical client in Andover, MA. This person will lead, develop, and qualify purification techniques for biologics at both pilot and bench scale. This role involves hands-on execution of purification processes using a variety of unit operations including precipitation, depth filtration, tangential flow filtration (TFF), and chromatography. The scientist will support technology transfer, process troubleshooting, and continuous improvement initiatives.________________________________________Key Responsibilities:?Lead and execute purification processing using precipitation, depth filtration, TFF, and chromatography.?Develop and characterize purification processes for polysaccharide program, including second-generation process development.?Independently plan, design, and execute downstream experiments to support technology transfer of program..?Operate and maintain downstream equipment such as AKTAs and Repligen TFF systems, and analytical tools including SoloVPE, Stunner, and Raman spectroscopy.?Analyze data, prepare technical reports, and present findings to internal teams.?Support manufacturing investigations and troubleshoot purification processes.?Drive continuous improvement initiatives including 5S, TPM, and operational excellence.?Plan and execute critical material production campaigns independently.?Collaborate cross-functionally with project teams to ensure alignment and effective communication.- Familiarity with mRNA Lipid nano particle formulation and Final Drug Product (FDP) processesWe 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":"Downstream Scientist","City":"Andover","ExpirationDate":null,"PriorityOrder":0,"Requirements":"-Hands on exp with depth filtration, scale down model exp**, TFF, UFDF, normal filtration - must know all these techniques at a minimum-Experience supporting r\u0026d AND manufacturing - cannot just be manufacturing -2+ years of downstream purification exp in a pharmaceutical setting (can be small or large molecule products)","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":45.0000,"SalaryLow":36.0000,"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)\/"}

We are looking for a Downstream Scientist to support our pharmaceutical client in Andover, MA. This person will lead, develop, and qualify purification techniques for biologics at both pilot and... bench scale. This role involves hands-on execution of purification processes using a variety of unit operations including precipitation, depth filtration, tangential flow filtration (TFF), and chromatography. The scientist will support technology transfer, process troubleshooting, and continuous improvement initiatives.________________________________________Key Responsibilities:?Lead and execute purification processing using precipitation, depth filtration, TFF, and chromatography.?Develop and characterize purification processes for polysaccharide program, including second-generation process development.?Independently plan, design, and execute downstream experiments to support technology transfer of program..?Operate and maintain downstream equipment such as AKTAs and Repligen TFF systems, and analytical tools including SoloVPE, Stunner, and Raman spectroscopy.?Analyze data, prepare technical reports, and present findings to internal teams.?Support manufacturing investigations and troubleshoot purification processes.?Drive continuous improvement initiatives including 5S, TPM, and operational excellence.?Plan and execute critical material production campaigns independently.?Collaborate cross-functionally with project teams to ensure alignment and effective communication.- Familiarity with mRNA Lipid nano particle formulation and Final Drug Product (FDP) processesWe 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 21, 2026

Lower Gwynedd, PA

|

Software Engineering

|

Contract

|

$20 - $25 (hourly estimate)

{"JobID":521451,"JobType":["Contract"],"EmployerID":null,"Location":{"Latitude":-75.22,"Longitude":40.15,"Distance":null},"State":"Pennsylvania","Zip":"19002","ReferenceID":"KPD-ce21253a-35e1-414d-af96-84e505c427c8","PostedDate":"\/Date(1776797784000)\/","Description":"Insight Global is currently seeking a GenAI Engineer for a large pharmaceutical client. This person will be joining a large project focused on automated document processing. This person will be responsible for taking technical requirements and developing POC of a GenAI tool focused on document processing within the pharmaceutical drug development process, and should have extensive experience with relevant tools used for this process along with GenAI experience such as RAG/Vector Databases.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":"GenAI Engineer - INTL India","City":"Lower Gwynedd","ExpirationDate":null,"PriorityOrder":0,"Requirements":"-3+ years of experience as a GenAI Engineer-LLM, RAG, Vector database development-Automated document processing experience-AWS Textract-Agentic framework experience","Skills":"","Industry":"Software 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":25.0000,"SalaryLow":20.0000,"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 currently seeking a GenAI Engineer for a large pharmaceutical client. This person will be joining a large project focused on automated document processing. This person will be... responsible for taking technical requirements and developing POC of a GenAI tool focused on document processing within the pharmaceutical drug development process, and should have extensive experience with relevant tools used for this process along with GenAI experience such as RAG/Vector Databases.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 08, 2026

Rocky Mount, NC

|

QA

|

Contract

|

$57 - $71 (hourly estimate)

{"JobID":528624,"JobType":["Contract"],"EmployerID":null,"Location":{"Latitude":-77.81,"Longitude":35.95,"Distance":null},"State":"North Carolina","Zip":"27804","ReferenceID":"RAL-8845da0e-0dd7-46b6-9d24-073d8a17cb8f","PostedDate":"\/Date(1778279639000)\/","Description":"Insight Global is seeking an experienced Investigation Coach to support and elevate investigation quality and consistency across a pharmaceutical manufacturing site in Rocky Mount, NC. This role will focus on hands-on coaching and skill development for a small group of investigators (typically coaching ~3 investigators per coach), with an emphasis on strengthening specific investigative competencies.While also owning investigations end-to-end, the Coach will act as a technical mentor and quality reviewer, helping investigators improve execution, critical thinking, and application of investigation standards. Coaching assignments will be skill-based, grouping investigators by their developmental needs (e.g., root cause analysis, CAPA effectiveness).?Provide targeted, skill-based coaching to assigned investigators, focusing on specific development areas such as: oRoot cause analysisoCAPA development and effectivenessoInvestigation structure, clarity, and documentation quality?Review investigations at key milestones to: oIdentify gaps in logic, analysis, or documentationoProvide clear, actionable feedback to drive improvement?Serve as a subject matter expert and sounding board for complex or high-impact investigations?Partner closely with Investigation Managers to: oAlign coaching focus areas to team needsoSupport consistent investigation standards across the organizationWe 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":"Quality Investigation Coach","City":"Rocky Mount","ExpirationDate":null,"PriorityOrder":0,"Requirements":"M1, Yellow Belt, or higher Six Sigma qualification 5+ years of experience in pharmaceutical investigations and/or Quality AssuranceStrong background in: o Deviation investigationso Root cause analysis methodologieso CAPA development and assessmentDemonstrated ability to mentor, coach, or review the work of other investigatorsDeep understanding of regulated manufacturing environments and quality systemsExcellent communication skills with the ability to deliver constructive, confidence-building feedback","Skills":"","Industry":"QA","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":71.0000,"SalaryLow":56.8000,"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 experienced Investigation Coach to support and elevate investigation quality and consistency across a pharmaceutical manufacturing site in Rocky Mount, NC. This role will... focus on hands-on coaching and skill development for a small group of investigators (typically coaching ~3 investigators per coach), with an emphasis on strengthening specific investigative competencies.While also owning investigations end-to-end, the Coach will act as a technical mentor and quality reviewer, helping investigators improve execution, critical thinking, and application of investigation standards. Coaching assignments will be skill-based, grouping investigators by their developmental needs (e.g., root cause analysis, CAPA effectiveness).?Provide targeted, skill-based coaching to assigned investigators, focusing on specific development areas such as: oRoot cause analysisoCAPA development and effectivenessoInvestigation structure, clarity, and documentation quality?Review investigations at key milestones to: oIdentify gaps in logic, analysis, or documentationoProvide clear, actionable feedback to drive improvement?Serve as a subject matter expert and sounding board for complex or high-impact investigations?Partner closely with Investigation Managers to: oAlign coaching focus areas to team needsoSupport consistent investigation standards across the organizationWe 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

North York, ON

|

Engineering (Non IT)

|

Perm

|

$85 - $100000 (hourly estimate)

{"JobID":533311,"JobType":["Perm"],"EmployerID":null,"Location":{"Latitude":0,"Longitude":0,"Distance":null},"State":"Ontario","Zip":"M9L 2","ReferenceID":"TOR-f178f934-0620-4aad-a0af-3c47195c81ea","PostedDate":"\/Date(1779400207000)\/","Description":"We?re seeking a Production Operations Supervisor to lead day-to-day manufacturing operations within a regulated production environment. This role is responsible for delivering results across safety, quality, and productivity while leading frontline teams and driving continuous improvement initiatives.This is a hands-on leadership role suited for early-career supervisors (3?5 years of experience) who have demonstrated ownership of shift performance, team leadership, and operational improvements in industries such as pharmaceutical, food, CPG, automotive, or oil and gas.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":"Supervisor, Production","City":"North York","ExpirationDate":null,"PriorityOrder":0,"Requirements":"? 3?5 years of supervisory or team leadership experience in a manufacturing or production environment.? Experience in regulated or process-driven industries (pharma, food/CPG, automotive, oil \u0026 gas).? Proven ability to lead shift-based operations and manage team performance.? Demonstrated track record of driving improvements in safety, quality, or continuous improvement (CI).? Experience managing frontline employees (directly or through supervisors), ideally within larger teams (~25?30 per shift).? Strong problem-solving and decision-making skills in fast-paced environments.? Clear and effective communication skills.? Stable work history (no pattern of short-term roles).","Skills":"? Experience in pharmaceutical or solid dose manufacturing environments.? Exposure to cGMP, SOPs, and regulatory compliance standards.? Post-secondary education in a relevant technical or scientific field.? Experience using ERP systems (e.g., SAP) and Microsoft Office tools.? Experience acting as a project or initiative lead within operations.","Industry":"Engineering (Non IT)","Country":"Canada","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":100000.0000,"SalaryLow":85.0000,"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)\/"}

We?re seeking a Production Operations Supervisor to lead day-to-day manufacturing operations within a regulated production environment. This role is responsible for delivering results across safety,... quality, and productivity while leading frontline teams and driving continuous improvement initiatives.This is a hands-on leadership role suited for early-career supervisors (3?5 years of experience) who have demonstrated ownership of shift performance, team leadership, and operational improvements in industries such as pharmaceutical, food, CPG, automotive, or oil and gas.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 09, 2026

Morris Plains, NJ

|

Engineering (Non IT)

|

Contract

|

$36 - $45 (hourly estimate)

{"JobID":516957,"JobType":["Contract"],"EmployerID":null,"Location":{"Latitude":-74.4824,"Longitude":40.8432,"Distance":null},"State":"New Jersey","Zip":"07950","ReferenceID":"NNJ-343f47ad-fee1-43ac-94a1-db8e0d4de799","PostedDate":"\/Date(1775738720000)\/","Description":"Insight Global is looking for an investigator for one of our top pharmaceutical clients to support their site in Morris Plains, NJ. This role will author and oversee deviations, investigations, CAPAs, and related reports to ensure closure within the established timelines for the manufacturing department.This role opens deviations, assesses their criticality within required timeframes, and evaluates any potential product impact in alignment with batch release activities. The specialist authors and owns investigations from initiation through closure, applying process knowledge and root cause analysis tools to identify true root causes of product and process deviations. They ensure all critical and major investigations are robust, accurate, complete, and fully defendable, and they design and execute experiments or test runs as needed to support investigation findings. Working cross-functionally, the specialist collaborates with Manufacturing, Quality Control, Engineering, and other partners to analyze deviations, determine impact, and ensure production continues in a compliant manner with appropriate documentation.In addition, the role is responsible for generating and documenting effective corrective and preventive actions (CAPAs) that address identified root causes and prevent recurrence. The specialist ensures CAPAs are implemented through appropriate GMP systems, such as manufacturing batch record revisions, training updates, or procedural changes, and monitors their progress through structured effectiveness checks. They also communicate with facilities and training teams to reinforce quality behaviors and support awareness initiatives, while contributing to SOP updates as needed to maintain compliance and drive continuous improvement.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":"Investigator","City":"Morris Plains","ExpirationDate":null,"PriorityOrder":0,"Requirements":"2-5 years of experience within pharmaceutical environmentGMP, Aseptic, sterile experience Strong documentation skills both written and verbal Bachelor\u0027s Degree in scientific related field","Skills":"Cell and gene therapy","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":45.0000,"SalaryLow":36.0000,"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 looking for an investigator for one of our top pharmaceutical clients to support their site in Morris Plains, NJ. This role will author and oversee deviations, investigations,... CAPAs, and related reports to ensure closure within the established timelines for the manufacturing department.This role opens deviations, assesses their criticality within required timeframes, and evaluates any potential product impact in alignment with batch release activities. The specialist authors and owns investigations from initiation through closure, applying process knowledge and root cause analysis tools to identify true root causes of product and process deviations. They ensure all critical and major investigations are robust, accurate, complete, and fully defendable, and they design and execute experiments or test runs as needed to support investigation findings. Working cross-functionally, the specialist collaborates with Manufacturing, Quality Control, Engineering, and other partners to analyze deviations, determine impact, and ensure production continues in a compliant manner with appropriate documentation.In addition, the role is responsible for generating and documenting effective corrective and preventive actions (CAPAs) that address identified root causes and prevent recurrence. The specialist ensures CAPAs are implemented through appropriate GMP systems, such as manufacturing batch record revisions, training updates, or procedural changes, and monitors their progress through structured effectiveness checks. They also communicate with facilities and training teams to reinforce quality behaviors and support awareness initiatives, while contributing to SOP updates as needed to maintain compliance and drive continuous improvement.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/.

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