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Jun 08, 2026

Upper Merion, PA

|

Computer Engineering

|

Contract-to-perm

|

$28 - $35 (hourly estimate)

{"JobID":538968,"JobType":["Contract-to-perm"],"EmployerID":null,"Location":{"Latitude":-75.38,"Longitude":40.09,"Distance":null},"State":"Pennsylvania","Zip":"19406","ReferenceID":"PHL-ca4db6e6-0866-4806-9e1e-d2b18635944c","PostedDate":"\/Date(1780942961000)\/","Description":"One of our large biopharmaceutical clients is seeking a CSV specialist to join their team for a Windows 11 upgrade. This role focuses on assessing system impact, executing validation deliverables, coordinating with the DeltaV and MES team to ensuring that all upgraded platforms meet regulatory, data integrity, and business continuity requirements. The ideal candidate brings deep experience in Computer System Validation (CSV) within a regulated biopharmaceutical environment and is comfortable working at the intersection of IT infrastructure and GMP operations.Key ResponsibilitiesWork on CSV activities related to the Windows 11 operating system upgrade across GxP-impacted systems and applications.Perform system impact assessments, risk evaluations, and gap analyses to determine validation scope.Develop and execute validation documentation, including URS, FRS, RTM, IQ/OQ/PQ, and validation summary reports.Partner with IT, Quality Assurance, and system owners to ensure compliant implementation and smooth transition of validated systems.Review vendor documentation and assess suitability for GMP use.Ensure all changes follow change control, deviation management, and data integrity requirements.Support testing activities, including regression testing, functional verification, and system compatibility checks.Maintain clear documentation and traceability throughout the validation lifecycle.Provide guidance on regulatory expectations related to OS upgrades, cybersecurity, and system lifecycle management.Support audits and inspections by providing validation evidence and subject-matter expertise.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":"CSV Specialist","City":"Upper Merion","ExpirationDate":null,"PriorityOrder":0,"Requirements":"Bachelor?s degree in Engineering, Computer Science, Life Sciences, or related field.3?7+ years of experience in a GMP biopharmaceutical, biotech, or pharmaceutical environment.","Skills":"Kneat experienceExperience with CSV or Validation","Industry":"Computer Engineering","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":35.0000,"SalaryLow":28.0000,"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)\/"}

One of our large biopharmaceutical clients is seeking a CSV specialist to join their team for a Windows 11 upgrade. This role focuses on assessing system impact, executing validation deliverables,... coordinating with the DeltaV and MES team to ensuring that all upgraded platforms meet regulatory, data integrity, and business continuity requirements. The ideal candidate brings deep experience in Computer System Validation (CSV) within a regulated biopharmaceutical environment and is comfortable working at the intersection of IT infrastructure and GMP operations.Key ResponsibilitiesWork on CSV activities related to the Windows 11 operating system upgrade across GxP-impacted systems and applications.Perform system impact assessments, risk evaluations, and gap analyses to determine validation scope.Develop and execute validation documentation, including URS, FRS, RTM, IQ/OQ/PQ, and validation summary reports.Partner with IT, Quality Assurance, and system owners to ensure compliant implementation and smooth transition of validated systems.Review vendor documentation and assess suitability for GMP use.Ensure all changes follow change control, deviation management, and data integrity requirements.Support testing activities, including regression testing, functional verification, and system compatibility checks.Maintain clear documentation and traceability throughout the validation lifecycle.Provide guidance on regulatory expectations related to OS upgrades, cybersecurity, and system lifecycle management.Support audits and inspections by providing validation evidence and subject-matter expertise.We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com.To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/.

Apr 22, 2026

Berkeley, CA

|

Laboratory Technician

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Contract-to-perm

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$28 - $35 (hourly estimate)

{"JobID":521904,"JobType":["Contract-to-perm"],"EmployerID":null,"Location":{"Latitude":-122.3,"Longitude":37.87,"Distance":null},"State":"California","Zip":"94710","ReferenceID":"SFR-6036497a-9ca3-465a-8154-76b05e37200e","PostedDate":"\/Date(1776872483000)\/","Description":"We are seeking a highly motivated Drug Product Specialist to join our Cell Therapy Manufacturing team. This role is critical in supporting aseptic operations and ensuring compliance with GMP standards for drug product filling and related processes. The ideal candidate will have hands-on experience in aseptic techniques, drug product handling, and GMP environments.Perform environmental monitoring in classified areasPrepare solutions and manage inventory for manufacturing operationsSupport aseptic processes including drug product filling and visual inspectionMaintain and complete electronic batch records accuratelyParticipate in gowning qualification, aseptic training, and media fill exercisesAssist in routine operations and troubleshooting within GMP guidelinesCollaborate with cross-functional teams to ensure smooth production flowWe 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":"Drug Product Specialist","City":"Berkeley","ExpirationDate":null,"PriorityOrder":0,"Requirements":"2?3 years of experience Aseptic qualifications or training (media fill, gowning certification)Experience in drug product filling, visual inspection, or pharmaceutical compoundingStrong understanding of GMP complianceBackground in manufacturing processes such as silicon chip production or similar regulated environments","Skills":"","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":35.0000,"SalaryLow":28.0000,"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 seeking a highly motivated Drug Product Specialist to join our Cell Therapy Manufacturing team. This role is critical in supporting aseptic operations and ensuring compliance with GMP... standards for drug product filling and related processes. The ideal candidate will have hands-on experience in aseptic techniques, drug product handling, and GMP environments.Perform environmental monitoring in classified areasPrepare solutions and manage inventory for manufacturing operationsSupport aseptic processes including drug product filling and visual inspectionMaintain and complete electronic batch records accuratelyParticipate in gowning qualification, aseptic training, and media fill exercisesAssist in routine operations and troubleshooting within GMP guidelinesCollaborate with cross-functional teams to ensure smooth production flowWe are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com.To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/.

Jun 15, 2026

Raleigh, NC

|

Engineering (Non IT)

|

Contract

|

$44 - $55 (hourly estimate)

{"JobID":541504,"JobType":["Contract"],"EmployerID":null,"Location":{"Latitude":-78.65,"Longitude":35.82,"Distance":null},"State":"North Carolina","Zip":"27612","ReferenceID":"RAL-66986330-b279-462e-a5ee-54c82f960fd9","PostedDate":"\/Date(1781536921000)\/","Description":"A global biopharmaceutical organization is seeking a Method Transfer and Validation Scientist to support the Quality Control organization within a regulated manufacturing environment. This individual will play a key role in transferring, validating, and maintaining microbiological test methods to ensure product quality, compliance, and operational readiness.This is a hands on laboratory role that requires strong experience with microbiology testing methods in a GMP environment.Key Responsibilities?Execute method transfer and validation activities for microbiological assays within a Quality Control laboratory ?Perform routine and non routine microbiology testing, including: ?Bioburden testing?Endotoxin testing?Sterility testing?Microbial identification as needed?Draft, execute, and review validation protocols, reports, and technical documentation?Analyze and interpret laboratory data to ensure accuracy, completeness, and compliance with regulatory requirements?Support investigations related to OOS, deviations, and assay performance and assist with root cause analysis and CAPA activities?Collaborate cross functionally with Quality Control, Quality Assurance, Manufacturing, and MSAT teams to support successful method transfers and process readiness?Update and maintain SOPs, test methods, and laboratory documentation to ensure continued compliance?Ensure all activities adhere to cGMP standards, data integrity requirements, and regulatory guidelines?Must be comfortable working either shift as follows: ?Shift A: Sun-Weds (4x10)?Shift B: Weds-Sat (4x10)We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com.To learn more about how we collect, keep, and process your private information, please review Insight Global\u0027s Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/.","Title":"Microbiology Method Transfer Scientist","City":"Raleigh","ExpirationDate":null,"PriorityOrder":0,"Requirements":"- 3-5 years of post-graduate relevant experience -Experience with various microbiology testing in the lab (Bioburden + Endotoxin is a must)-Experience working in a pharmaceutical setting -Experience supporting method validation, method transfer, or assay qualification activities","Skills":"","Industry":"Engineering (Non IT)","Country":"US","Division":"AF\u0026E","Office":null,"IsRemoteJob":false,"IsInternalJob":false,"ExtraValues":null,"__RecordIndex":0,"__OrdinalPosition":0,"__Timestamp":0,"Status":null,"ApplicantCount":0,"SubmittalCount":0,"ApplicationToHireRatio":0,"JobDuration":null,"SalaryHigh":55.0000,"SalaryLow":44.0000,"PayRateOvertime":0,"PayRateStraight":0,"Filled":0,"RemainingOpenings":0,"TotalOpenings":0,"Visa":null,"ClearanceType":null,"IsClearanceRequired":false,"IsHealthcare":false,"IsRemote":false,"EndClient":null,"JobCreatedDate":"\/Date(-62135578800000)\/","JobModifiedDate":"\/Date(-62135578800000)\/"}

A global biopharmaceutical organization is seeking a Method Transfer and Validation Scientist to support the Quality Control organization within a regulated manufacturing environment. This individual... will play a key role in transferring, validating, and maintaining microbiological test methods to ensure product quality, compliance, and operational readiness.This is a hands on laboratory role that requires strong experience with microbiology testing methods in a GMP environment.Key Responsibilities?Execute method transfer and validation activities for microbiological assays within a Quality Control laboratory ?Perform routine and non routine microbiology testing, including: ?Bioburden testing?Endotoxin testing?Sterility testing?Microbial identification as needed?Draft, execute, and review validation protocols, reports, and technical documentation?Analyze and interpret laboratory data to ensure accuracy, completeness, and compliance with regulatory requirements?Support investigations related to OOS, deviations, and assay performance and assist with root cause analysis and CAPA activities?Collaborate cross functionally with Quality Control, Quality Assurance, Manufacturing, and MSAT teams to support successful method transfers and process readiness?Update and maintain SOPs, test methods, and laboratory documentation to ensure continued compliance?Ensure all activities adhere to cGMP standards, data integrity requirements, and regulatory guidelines?Must be comfortable working either shift as follows: ?Shift A: Sun-Weds (4x10)?Shift B: Weds-Sat (4x10)We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com.To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/.

May 06, 2026

Newport News, VA

|

Engineering (Non IT)

|

Contract

|

$56 - $70 (hourly estimate)

{"JobID":527288,"JobType":["Contract"],"EmployerID":null,"Location":{"Latitude":-76.51,"Longitude":37.07,"Distance":null},"State":"Virginia","Zip":"23603","ReferenceID":"RAL-55a6fcc7-5453-48ae-9659-d2b78de0c377","PostedDate":"\/Date(1778080726000)\/","Description":"The Construction Manager will serve as the single point of coordination for safety, quality, schedule, and documentation, working alongside specialty trade contractors. This is not a traditional GC role ? the CM acts as the owner?s on-site coordinator and quality lead.Project \u0026 Construction Coordination?Act as the day-to-day Construction Manager on site, coordinating multiple specialty contractors performing the work.?Track and manage daily activities, schedule adherence, and resource loading.?Support enabling work, shutdown execution, and post-shutdown/start-up activities.?Maintain situational awareness with active manufacturing lines on both sides of the work area during shutdown.Quality Control \u0026 Documentation ?Serve as the single point of quality control for the project.?Verify material receipts to confirm they are per specification.?Document installation activities and confirm compliance with drawings and project requirements.?Sign off on: oPressure testsoConformity / quality inspection reports?Maintain detailed records of: oQuality inspectionsoAs-built conditionsoAny deviations from construction drawings?Ensure GMP documentation expectations are met.Safety \u0026 Compliance?Oversee site safety compliance during high-risk shutdown activities.?Coordinate safe access and work sequencing in live manufacturing adjacent areas.?Interface with site EHS as needed to ensure adherence to safety and GMP requirements.Reporting \u0026 Systems?Submit daily construction reports in Procore, including progress, manpower, safety, and quality observations.?Maintain accurate project logs and documentation for stakeholder visibility.Permitting \u0026 Inspections?Coordinate directly with Newport News permitting officials to support required permits and inspections.?Facilitate inspection readiness and on-site walkthroughs as 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":"Construction Manager","City":"Newport News","ExpirationDate":null,"PriorityOrder":0,"Requirements":"10+ years of construction or industrial project experienceStrong background in: oConcreteoIndustrial equipment installationoElectrical systems and controls (knowledgeable, not performing hands-on work)Ability to coordinate work safely around live operationsStrong documentation, inspection, and quality mindsetComfortable acting as the central coordinator across contractors, engineers, and owner stakeholders","Skills":"OSHA 30 certificationExperience working within active manufacturing environmentsPrior experience leading or coordinating projects in: oGMP-regulated facilitiesoFood, pharmaceutical, or industrial manufacturing environmentsExperience managing shutdowns or turnarounds","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)\/"}

The Construction Manager will serve as the single point of coordination for safety, quality, schedule, and documentation, working alongside specialty trade contractors. This is not a traditional GC... role ? the CM acts as the owner?s on-site coordinator and quality lead.Project & Construction Coordination?Act as the day-to-day Construction Manager on site, coordinating multiple specialty contractors performing the work.?Track and manage daily activities, schedule adherence, and resource loading.?Support enabling work, shutdown execution, and post-shutdown/start-up activities.?Maintain situational awareness with active manufacturing lines on both sides of the work area during shutdown.Quality Control & Documentation ?Serve as the single point of quality control for the project.?Verify material receipts to confirm they are per specification.?Document installation activities and confirm compliance with drawings and project requirements.?Sign off on: oPressure testsoConformity / quality inspection reports?Maintain detailed records of: oQuality inspectionsoAs-built conditionsoAny deviations from construction drawings?Ensure GMP documentation expectations are met.Safety & Compliance?Oversee site safety compliance during high-risk shutdown activities.?Coordinate safe access and work sequencing in live manufacturing adjacent areas.?Interface with site EHS as needed to ensure adherence to safety and GMP requirements.Reporting & Systems?Submit daily construction reports in Procore, including progress, manpower, safety, and quality observations.?Maintain accurate project logs and documentation for stakeholder visibility.Permitting & Inspections?Coordinate directly with Newport News permitting officials to support required permits and inspections.?Facilitate inspection readiness and on-site walkthroughs as 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/.

May 27, 2026

Clayton, NC

|

Engineering (Non IT)

|

Perm

|

$98k - $108k (estimate)

{"JobID":534751,"JobType":["Perm"],"EmployerID":null,"Location":{"Latitude":-78.45,"Longitude":35.64,"Distance":null},"State":"North Carolina","Zip":"27520","ReferenceID":"RAL-45611053-f4c4-49a4-a7f1-c7c931120980","PostedDate":"\/Date(1779912739000)\/","Description":"? Implementation of environmental \u0026 safety programs? Support EHS aspects as required including interactions with various regulatory and governmental agencies ensuring compliance with local, county, state and federal requirements? Provide expertise \u0026 solutions to relevant personnel \u0026 projects to resolve known or potential issues? Conduct EHS assessments/inspections \u0026 work with area managers to ensure timely remediation of identified issues? Provide training \u0026 tools for the core processes to improve performanceCommunicate EHS performance statistics on a routine basisWe 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":"Health \u0026 Safety Professional II","City":"Clayton","ExpirationDate":null,"PriorityOrder":0,"Requirements":"- industrial hygiene background -GMP experience ? Bachelor\u0027s Degree in Environmental Health \u0026 Safety, Safety Management, or related field of study from an accredited university required and a minimum of one (1) year of experience in a safety environment required, preferably in a pharmaceutical manufacturing environmentIn lieu of Bachelor\u0027s Degree with one (1) year of experience, may consider an Associate\u0027s Degree in Environmental Health \u0026 Safety, Safety Management, or related field of study from an accredited college or university with a minimum of three (3) years of experience in a safety environment required, preferably in a pharmaceutical manufacturing environment","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":108000.0000,"SalaryLow":98000.0000,"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)\/"}

? Implementation of environmental & safety programs? Support EHS aspects as required including interactions with various regulatory and governmental agencies ensuring compliance with local, county,... state and federal requirements? Provide expertise & solutions to relevant personnel & projects to resolve known or potential issues? Conduct EHS assessments/inspections & work with area managers to ensure timely remediation of identified issues? Provide training & tools for the core processes to improve performanceCommunicate EHS performance statistics on a routine basisWe 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 05, 2026

North Tonawanda, NY

|

Corporate Operations

|

Contract

|

$64 - $80 (hourly estimate)

{"JobID":526619,"JobType":["Contract"],"EmployerID":null,"Location":{"Latitude":-78.86,"Longitude":43.04,"Distance":null},"State":"New York","Zip":"14120","ReferenceID":"NNJ-9a381558-3198-46a5-ae1a-a31f77f010d8","PostedDate":"\/Date(1777990364000)\/","Description":"This Complaints Investigator role will support our medical device client by conducting end-to-end investigations on 10,000+ product complaints related to a women\u0027s health medical device. This role requires strong analytical skills, hands-on functional testing capability, and the ability to hit the ground running with minimal supervision while meeting weekly productivity metrics. Working fully on-site at a small, integrated manufacturing location of roughly 25 employees, the investigator will join a focused team of 7?8 and report directly to the Quality Manager. This is a 40-hour-per-week position requiring deep attention to detail, clear documentation, and consistent execution in a fast-paced quality environment. They will be handling these complains in the Trackwise QMS system (around 30+/day)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":"Complaints Investigator","City":"North Tonawanda","ExpirationDate":null,"PriorityOrder":0,"Requirements":"-BS Degree within science /engineering field-5+ years of Complaint investigations experience -Pharmaceutical or medical device complaints experience -Experience managing a volume of 30+ complaints per day -Strong QMS system experience","Skills":"-Remediation complaints investigation -Trackwise experience","Industry":"Corporate Operations","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":80.0000,"SalaryLow":64.0000,"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)\/"}

This Complaints Investigator role will support our medical device client by conducting end-to-end investigations on 10,000+ product complaints related to a women's health medical device. This role... requires strong analytical skills, hands-on functional testing capability, and the ability to hit the ground running with minimal supervision while meeting weekly productivity metrics. Working fully on-site at a small, integrated manufacturing location of roughly 25 employees, the investigator will join a focused team of 7?8 and report directly to the Quality Manager. This is a 40-hour-per-week position requiring deep attention to detail, clear documentation, and consistent execution in a fast-paced quality environment. They will be handling these complains in the Trackwise QMS system (around 30+/day)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 20, 2026

King Of Prussia, PA

|

Project Manager

|

Contract

|

$56 - $70 (hourly estimate)

{"JobID":532551,"JobType":["Contract"],"EmployerID":null,"Location":{"Latitude":-75.38,"Longitude":40.09,"Distance":null},"State":"Pennsylvania","Zip":"19406","ReferenceID":"KPD-9c856a79-a528-4760-bd4e-7cf4c69b40bd","PostedDate":"\/Date(1779303518000)\/","Description":"Insight Global is seeking a Senior Portfolio Manager to support enterprise-level portfolio execution across a complex IT organization. This individual will partner closely with IT leadership, internal teams, and external vendors to drive delivery across multiple high-visibility programs and projects. This role requires strong program/portfolio management expertise, financial acumen, and the ability to influence stakeholders while ensuring alignment to strategic priorities.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 Portfolio Manager","City":"King Of Prussia","ExpirationDate":null,"PriorityOrder":0,"Requirements":"? 8+ years of Program / Portfolio Management experience within IT? Strong project management fundamentals:? Project planning and execution? Critical path management? Risk, issue, and dependency tracking (RADIO framework)? Experience working within PPM tools (Clarity or similar) and understanding of portfolio management concepts? Proven ability to influence senior stakeholders and leadership teams? Strong communication and presentation skills (executive-level)? Experience working in vendor-heavy environmentsDemonstrated financial acumen managing large-scale budgets ($1M+)","Skills":"? Experience in pharmaceutical / life sciences environments? Experience with Clarity as a PPM tool","Industry":"Project Manager","Country":"US","Division":"IT","Office":null,"IsRemoteJob":false,"IsInternalJob":false,"ExtraValues":null,"__RecordIndex":0,"__OrdinalPosition":0,"__Timestamp":0,"Status":null,"ApplicantCount":0,"SubmittalCount":0,"ApplicationToHireRatio":0,"JobDuration":null,"SalaryHigh":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 Senior Portfolio Manager to support enterprise-level portfolio execution across a complex IT organization. This individual will partner closely with IT leadership,... internal teams, and external vendors to drive delivery across multiple high-visibility programs and projects. This role requires strong program/portfolio management expertise, financial acumen, and the ability to influence stakeholders while ensuring alignment to strategic priorities.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 12, 2026

Uwchlan, PA

|

Architect

|

Contract

|

$66 - $83 (hourly estimate)

{"JobID":529514,"JobType":["Contract"],"EmployerID":null,"Location":{"Latitude":-75.63,"Longitude":40.03,"Distance":null},"State":"Pennsylvania","Zip":"19341","ReferenceID":"KPD-56c1885e-bb7d-44ac-8014-f4fd503eba6a","PostedDate":"\/Date(1778610399000)\/","Description":"One of Insight Global\u0027s clients is Senior Solution Architect specializing in SAP Quality Management to partner with Plan-to-Produce and Operations teams in delivering technology-enabled business solutions. This role is responsible for defining strategic direction, support models, and best-in-class solutions across quality processes, including integration with LIMS and MES systems. The architect will lead the design and delivery of SAP QM capabilities, ensuring alignment with enterprise standards, regulatory requirements, and overall business objectives. This individual will translate complex business needs into scalable technical solutions while managing system enhancements, support operations, and release cycles. The role also includes driving SLA performance, maintaining system lifecycle documentation, and ensuring compliance with internal policies and industry regulations. Additionally, the Senior Solution Architect will collaborate across global teams, contribute to continuous improvement initiatives, and provide technical leadership within the organization. This position requires candidates to be willing to travel up to 10% of the time (26 days per year roughly) in the US and also is onsite in Exton, PA Tuesday - Thursday.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":"SAP QM Solutions Architect","City":"Uwchlan","ExpirationDate":null,"PriorityOrder":0,"Requirements":"- 5+ years of SAP Quality Management (QM) expertise, including deep functional and technical knowledge- Experience integrating SAP QM with SAP PP and EWM- Hands-on experience with SAP S/4HANA implementations, including 2?3+ full lifecycle (end-to-end) implementations- Strong understanding of SAP QM configurations, including quality planning, inspections (inbound, in-process, outbound), notifications, batch management, traceability, and reporting- Experience working with LIMS and/or MES integrations with SAP- Proven ability to lead delivery and collaborate across global teams- Experience managing support teams, SLAs, and release cycles, including regression testing- Strong knowledge of master data management and data cleansing processes","Skills":"- SAP S4Hana QM certification- Experience in Pharmaceutical, Life Science, or Healthcare industry","Industry":"Architect","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":82.7500,"SalaryLow":66.2000,"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)\/"}

One of Insight Global's clients is Senior Solution Architect specializing in SAP Quality Management to partner with Plan-to-Produce and Operations teams in delivering technology-enabled business... solutions. This role is responsible for defining strategic direction, support models, and best-in-class solutions across quality processes, including integration with LIMS and MES systems. The architect will lead the design and delivery of SAP QM capabilities, ensuring alignment with enterprise standards, regulatory requirements, and overall business objectives. This individual will translate complex business needs into scalable technical solutions while managing system enhancements, support operations, and release cycles. The role also includes driving SLA performance, maintaining system lifecycle documentation, and ensuring compliance with internal policies and industry regulations. Additionally, the Senior Solution Architect will collaborate across global teams, contribute to continuous improvement initiatives, and provide technical leadership within the organization. This position requires candidates to be willing to travel up to 10% of the time (26 days per year roughly) in the US and also is onsite in Exton, PA Tuesday - Thursday.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 11, 2025

San Diego, CA

|

Training

|

Contract-to-perm

|

$68 - $85 (hourly estimate)

{"JobID":465821,"JobType":["Contract-to-perm"],"EmployerID":null,"Location":{"Latitude":-117.19,"Longitude":32.95,"Distance":null},"State":"California","Zip":"92130","ReferenceID":"SDG-04eba089-f1cb-427f-b631-763cbdab0c60","PostedDate":"\/Date(1762822192000)\/","Description":"A Pharmaceutical company based in San Diego, CA is seeking a Sr. Manager of Technology Enablement \u0026 Adoption (TEA) to join their team. The Sr. Manager of TEA will be responsible for designing, launching, and leading this new program from the ground up. This individual will build and manage a team that drives technology engagement, learning, and adoption across the enterprise ? ensuring that the end client realizes the full value of its digital investments.Design and establish the Technology Enablement \u0026 Adoption (TEA) program, including its strategy, operating model, governance, and success metricsStrategic partner with IT, HR, Corporate Communications, and Business Unit leaders to align enablement initiatives with organizational goalsDefine frameworks for measuring adoption, user satisfaction, and value realization from digital tools and platformsBuild, lead, and mentor a team of enablement professionals focused on training, communication, user community building, and change managementFoster a collaborative, learning-oriented culture within the team and across stakeholder groupsDrive adoption of enterprise technology platforms (e.g., Generative AI tools, Cyber Security, collaboration tools, analytics platforms, automation solutions)Create and manage targeted communication and learning programs to help employees use technology effectivelyCultivate a community network that creates a community of users across all levels to ensure there is engagement, peer-to-peer learning and knowledge sharingCreate and facilitate organizational Hackathons and top-down gamification elements that drive excitement and outcomesDevelop and implement change management strategies for major technology initiativesPartner with Corporate Communications to craft compelling narratives around the ?why? and ?how? of technology transformationsServe as a visible advocate and champion for digital enablement across the organizationEstablish feedback mechanisms to capture user experience and adoption insightsLeverage data to continuously optimize enablement strategies and improve outcomesEstablish feedback loops and analytics to measure adoption effectiveness, ROI, RWH, and technology utilization trendsReport progress through dashboards and scorecards that communicate impact to executivesCapture user stories across the company and help to paint a picture of how we are driving literacy, education, and adoption across the company in an efficient mannerWe 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. Manager - Training Enablement \u0026 Adoption","City":"San Diego","ExpirationDate":null,"PriorityOrder":0,"Requirements":"?Bachelor?s degree in Business, Information Technology, Organizational Development, or related field?7+ years of experience in technology enablement, digital adoption, learning \u0026 development, or change management?2+ years of people management experience?Proven success designing and implementing enterprise enablement and adoption programs?Strong understanding of change management methodologies and communication strategies?Exceptional cross-functional stakeholder management, facilitation, and storytelling skills?Exceptional communicator, written and oral strengths, any levels?Experience in a life sciences, healthcare, or regulated industry?Familiarity with digital workplace technologies (e.g., Microsoft 365, SharePoint, ServiceNow, analytics tools)","Skills":"","Industry":"Training","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":85.0000,"SalaryLow":68.0000,"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 Pharmaceutical company based in San Diego, CA is seeking a Sr. Manager of Technology Enablement & Adoption (TEA) to join their team. The Sr. Manager of TEA will be responsible for designing,... launching, and leading this new program from the ground up. This individual will build and manage a team that drives technology engagement, learning, and adoption across the enterprise ? ensuring that the end client realizes the full value of its digital investments.Design and establish the Technology Enablement & Adoption (TEA) program, including its strategy, operating model, governance, and success metricsStrategic partner with IT, HR, Corporate Communications, and Business Unit leaders to align enablement initiatives with organizational goalsDefine frameworks for measuring adoption, user satisfaction, and value realization from digital tools and platformsBuild, lead, and mentor a team of enablement professionals focused on training, communication, user community building, and change managementFoster a collaborative, learning-oriented culture within the team and across stakeholder groupsDrive adoption of enterprise technology platforms (e.g., Generative AI tools, Cyber Security, collaboration tools, analytics platforms, automation solutions)Create and manage targeted communication and learning programs to help employees use technology effectivelyCultivate a community network that creates a community of users across all levels to ensure there is engagement, peer-to-peer learning and knowledge sharingCreate and facilitate organizational Hackathons and top-down gamification elements that drive excitement and outcomesDevelop and implement change management strategies for major technology initiativesPartner with Corporate Communications to craft compelling narratives around the ?why? and ?how? of technology transformationsServe as a visible advocate and champion for digital enablement across the organizationEstablish feedback mechanisms to capture user experience and adoption insightsLeverage data to continuously optimize enablement strategies and improve outcomesEstablish feedback loops and analytics to measure adoption effectiveness, ROI, RWH, and technology utilization trendsReport progress through dashboards and scorecards that communicate impact to executivesCapture user stories across the company and help to paint a picture of how we are driving literacy, education, and adoption across the company in an efficient mannerWe 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 04, 2026

Dallas, TX

|

Mechanical Engineering

|

Perm

|

$25 - $45 (hourly estimate)

{"JobID":537702,"JobType":["Perm"],"EmployerID":null,"Location":{"Latitude":-96.76,"Longitude":32.79,"Distance":null},"State":"Texas","Zip":"75220","ReferenceID":"AUS-c4d57d91-6140-48e6-a479-cf1e76b5e1c1","PostedDate":"\/Date(1780577440000)\/","Description":"Dynamic Systems Inc. is hiring a QC Technician to support mechanical quality efforts in Dallas. This role is hands-on and field-based, ideal for someone with a mechanical mindset and a strong attention to detail.You?ll assist in inspecting mechanical installations, documenting findings, and supporting senior QC staff. The technician will work closely with project teams to ensure systems meet specifications and standards. This is a great opportunity for someone looking to grow in the mechanical contracting space.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":"QC Technician","City":"Dallas","ExpirationDate":null,"PriorityOrder":0,"Requirements":"Must Haves:Strong mechanical background (schooling, hands-on experience, or trade work)Go-getter mentality - proactive, eager to learn, and willing to take initiativeHardworking and dependable with a strong work ethicDetail-oriented - able to follow procedures and catch inconsistenciesComfortable working in field environments (job sites, construction zones)Basic understanding of tools, equipment, and mechanical systems","Skills":"Plusses:Prior experience in mechanical QC, commissioning, or TABExposure to semiconductor, pharmaceutical, or mission-critical projectsFamiliarity with industry codes (ASME, NFPA, IPC/IMC)Technical certifications or trade school background","Industry":"Mechanical Engineering","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":25.0000,"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)\/"}

Dynamic Systems Inc. is hiring a QC Technician to support mechanical quality efforts in Dallas. This role is hands-on and field-based, ideal for someone with a mechanical mindset and a strong... attention to detail.You?ll assist in inspecting mechanical installations, documenting findings, and supporting senior QC staff. The technician will work closely with project teams to ensure systems meet specifications and standards. This is a great opportunity for someone looking to grow in the mechanical contracting space.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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