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May 27, 2026

Akron, OH

|

Pharmacy Technician

|

Perm

|

$46k - $54k (estimate)

{"JobID":534878,"JobType":["Perm"],"EmployerID":null,"Location":{"Latitude":-81.42,"Longitude":41.1,"Distance":null},"State":"Ohio","Zip":"44278","ReferenceID":"DGW-7820b229-bc12-4cf9-8b37-430372237f2a","PostedDate":"\/Date(1779926272000)\/","Description":"Insight Global is looking for a self-directed IV Technician to join a home health healthcare provider sitting onsite in Akron, Ohio. In this position, the IV Technician will not insert IVs, but will prepare pharmacy orders for filling and compounding. It is not required to have IV or sterile experience to be successful in this role- the hired individuals will be trained and supported as necessary.This role is very independent and involves repetitive work, so the ideal candidate will be comfortable in this type of environment.This is a full-time, permanent role with competitive compensation starting at $22/hr and offers options for benefits.Key responsibilities are as follows:- Prepare prescriptions for filling, check records, and compound prescriptions- Perform sterile compounding operations consistent with relevant Ohio established protocols- Maintain compounding records, prescription logs, and ad hoc files as necessary- Keep pharmacy and compounding areas clean and up to code- Provide environmental monitoring and supply level oversight- Check in medication orders, stock, and monitor inventory quantities- Assist operations team in conducting physical inventory per policyWe 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":"IV Technician/Data Entry","City":"Akron","ExpirationDate":null,"PriorityOrder":0,"Requirements":"- High school diploma or GED- Registered with the Ohio Board of Pharmacy as a Nationally Certified Technician OR currently a Registered Pharmacy Technician can become Nationally Certified within 6 months of employment- Ability to perform basic pharmaceutical/math calculations","Skills":"- National Pharmacy Technician Certification- Experience with Sterile Compounding","Industry":"Pharmacy Technician","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":54080.0000,"SalaryLow":45760.0000,"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 a self-directed IV Technician to join a home health healthcare provider sitting onsite in Akron, Ohio. In this position, the IV Technician will not insert IVs, but will... prepare pharmacy orders for filling and compounding. It is not required to have IV or sterile experience to be successful in this role- the hired individuals will be trained and supported as necessary.This role is very independent and involves repetitive work, so the ideal candidate will be comfortable in this type of environment.This is a full-time, permanent role with competitive compensation starting at $22/hr and offers options for benefits.Key responsibilities are as follows:- Prepare prescriptions for filling, check records, and compound prescriptions- Perform sterile compounding operations consistent with relevant Ohio established protocols- Maintain compounding records, prescription logs, and ad hoc files as necessary- Keep pharmacy and compounding areas clean and up to code- Provide environmental monitoring and supply level oversight- Check in medication orders, stock, and monitor inventory quantities- Assist operations team in conducting physical inventory per policyWe 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/.

Oct 14, 2025

Mangum, NC

|

Engineering (Non IT)

|

Contract-to-perm

|

$40 - $50 (hourly estimate)

{"JobID":455085,"JobType":["Contract-to-perm"],"EmployerID":null,"Location":{"Latitude":-78.91,"Longitude":35.98,"Distance":null},"State":"North Carolina","Zip":"27712","ReferenceID":"RAL-e2a1425a-0928-4693-918f-5411c5a2af82","PostedDate":"\/Date(1760457076000)\/","Description":"Day to Day: A large pharmaceutical client in Durham is seeking a Sr. Maintenance Planner/Scheduler to join their team. The Senior Specialist, Planning and Scheduling will be accountable for the creation of a master production schedule that aligns with the global vaccine forecast and market requirements. The Sr. Planner will plan workloads and schedule operations for their assigned Operations Integrated Process Teams and /or Quality Operations Lab. This may include the creation and release of production/process orders for operations, scheduling/prioritization of lab activities, Manufacturing Execution System (MES) and dilution model creation, procurement/purchase of materials to enable schedules, and working closely with internal and external suppliers as well as customers to ensure timely deliveries. Key Functions?Creating and releasing process orders to the shop floor operations team. Leading scheduling meetings, maintaining and conveying production schedule?Supporting all relevant Manufacturing Execution System (MES) data entries for 24/7 production facility?Ensuring sufficient internally and externally sourced materials are available and released to meet all customer demands and downstream processes?Ensure that the accurate and current production plan is loaded into SAP and managed in Rapid Response?Working closely with Durham and West Point labs to ensure testing and release are aligned with inspection end dates Lots Release On-Time (LROT) and customer need dates Internal On-time in Full (iOTIF)?Acting as Supply Chain representative, as needed, in support of all Integrated Process Team meetings and initiatives (i.e. Tier meetings, Operational Readiness Management meetings (ORM), and upstream supplier and downstream customer meetings)?Managing the Inventory of Questionable Value (IQV) process for product set | Gathering information from site input departments and updating the IQV tool in SAP | Generating required discard documentation (FA33) and routing for approval?Reviewing the production schedule and Materials Requirement Planning outputs; making adjustments and interacts with supply network planning | Manages SAP master data, updating safety stock and reorder points?Monitoring inventory levels to avoid excess inventory, inventory shortages and/or inventory expiry?Providing quality notification (QN) and corrective action preventive action (CAPA) support?Developing and updating Planning standard operating proceduresWe 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":"Maintenance Planner","City":"Mangum","ExpirationDate":null,"PriorityOrder":0,"Requirements":"Required Education, Experience and Skills:?5 years of Planning \u0026 Scheduling supporting production, maintenance or calibration environments in industrial facilities ?Maintenance Background ?Minimum of three (3) years of experience working in a GMP regulated environment?Strong knowledge of Planning and Purchasing processes as well as Materials Requirements Planning (MRP)/Materials Production Scheduling (MPS) principles and methodologies?Experience using SAP?Team player with a positive attitude and the ability to maintain focus in difficult problem-solving situations","Skills":"Preferred Experience and Skills:?Experience in sterile vaccine manufacturing facility startup?APICS or CPIM certification?Lean Six Sigma Knowledge and Experience","Industry":"Engineering (Non IT)","Country":"US","Division":"AF\u0026E","Office":null,"IsRemoteJob":false,"IsInternalJob":false,"ExtraValues":null,"__RecordIndex":0,"__OrdinalPosition":0,"__Timestamp":0,"Status":null,"ApplicantCount":0,"SubmittalCount":0,"ApplicationToHireRatio":0,"JobDuration":null,"SalaryHigh":50.0000,"SalaryLow":40.0000,"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)\/"}

Day to Day: A large pharmaceutical client in Durham is seeking a Sr. Maintenance Planner/Scheduler to join their team. The Senior Specialist, Planning and Scheduling will be accountable for the... creation of a master production schedule that aligns with the global vaccine forecast and market requirements. The Sr. Planner will plan workloads and schedule operations for their assigned Operations Integrated Process Teams and /or Quality Operations Lab. This may include the creation and release of production/process orders for operations, scheduling/prioritization of lab activities, Manufacturing Execution System (MES) and dilution model creation, procurement/purchase of materials to enable schedules, and working closely with internal and external suppliers as well as customers to ensure timely deliveries. Key Functions?Creating and releasing process orders to the shop floor operations team. Leading scheduling meetings, maintaining and conveying production schedule?Supporting all relevant Manufacturing Execution System (MES) data entries for 24/7 production facility?Ensuring sufficient internally and externally sourced materials are available and released to meet all customer demands and downstream processes?Ensure that the accurate and current production plan is loaded into SAP and managed in Rapid Response?Working closely with Durham and West Point labs to ensure testing and release are aligned with inspection end dates Lots Release On-Time (LROT) and customer need dates Internal On-time in Full (iOTIF)?Acting as Supply Chain representative, as needed, in support of all Integrated Process Team meetings and initiatives (i.e. Tier meetings, Operational Readiness Management meetings (ORM), and upstream supplier and downstream customer meetings)?Managing the Inventory of Questionable Value (IQV) process for product set | Gathering information from site input departments and updating the IQV tool in SAP | Generating required discard documentation (FA33) and routing for approval?Reviewing the production schedule and Materials Requirement Planning outputs; making adjustments and interacts with supply network planning | Manages SAP master data, updating safety stock and reorder points?Monitoring inventory levels to avoid excess inventory, inventory shortages and/or inventory expiry?Providing quality notification (QN) and corrective action preventive action (CAPA) support?Developing and updating Planning standard operating proceduresWe 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 13, 2026

Holly Springs, NC

|

Engineering (Non IT)

|

Contract

|

$64 - $80 (hourly estimate)

{"JobID":518265,"JobType":["Contract"],"EmployerID":null,"Location":{"Latitude":-78.83,"Longitude":35.65,"Distance":null},"State":"North Carolina","Zip":"27540","ReferenceID":"RAL-e87fcf03-f20e-43f2-97fa-72c130604c14","PostedDate":"\/Date(1776111251000)\/","Description":"Role OverviewWe are seeking an MES Engineer with a strong testing mindset and hands-on Emerson Syncade experience to support a large pharmaceutical expansion in the Raleigh?Durham area. This role is highly execution-focused and ideal for someone who thrives in dynamic manufacturing environments, can quickly learn new processes, and excels at validating MES configurations, calculations, and workflows in support of tech transfer and paperless manufacturing initiatives.The engineer will play a key role in supporting Syncade MES configuration and testing across two drug substance manufacturing facilities, working closely with Automation, Manufacturing, Quality, CSV, and CQV teams to ensure systems are robust, compliant, and ready to support new products and downstream operations.Key ResponsibilitiesMES Configuration \u0026 Support?Support the design, configuration, and implementation of an Emerson Syncade Manufacturing Execution System to enable paperless manufacturing with full ERP/MES/DCS integration.?Implement and troubleshoot MES configuration changes across DeltaV DCS, DeltaV MES (Syncade), and a custom formula/parameter management system.?Debug configuration items and system behaviors within Syncade, ensuring issues are properly triaged to the correct teams and resolved without impacting manufacturing execution.?Migrate solution components between Syncade environments (e.g., development, test, and production).MES Testing \u0026 Validation (Primary Focus)?Translate functional and technical requirements into detailed MES test protocols.?Execute MES testing across a large volume of documents and system objects, including: oLibrary objectsoCalculations and parameter setupsoRecipes and workflowsoElectronic Batch Records (EBR)?Design and execute testing strategies for rapidly evolving or dynamically developed configurations and code.?Support infrastructure setup, software installation, recipe development, and User Acceptance Testing (UAT) in partnership with end users.?Support tech transfer activities by identifying gaps between source and target processes, particularly as global processes are transferred and localized (e.g., Denmark ? US).Manufacturing \u0026 Tech Transfer Support?Support technical runs and process execution for both established and new downstream manufacturing operations.?Troubleshoot MES-related issues during execution, identifying whether problems stem from process design, system configuration, or operational use.?Ensure MES workflows do not inadvertently constrain or embed inaccurate manufacturing processes during tech transfer or scale-up activities.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":"MES Engineer","City":"Holly Springs","ExpirationDate":null,"PriorityOrder":0,"Requirements":"Must-Have Qualifications?2+ years of experience designing, configuring, and implementing Manufacturing Execution Systems (MES).?2+ years of direct Emerson Syncade experience?Proven experience: oDebugging Syncade configuration items and system behaviorsoMigrating MES solution components between environmentsoExecuting and documenting MES testing activities?Experience working in a cGMP-regulated environment, with working knowledge of: FDA regulations, ISA-88 batch model, ISA-95, GAMP 5 21 CFR Part 11 (ERES)","Skills":"Preferred / Nice-to-Have Skills?Direct experience with Emerson DeltaV MES and DeltaV DCS.?Exposure to OSIsoft PI and/or InfoBatch.?Programming or configuration skills in one or more of the following: VBScript, XML / XPath / XSLT, SQL / T-SQL","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":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)\/"}

Role OverviewWe are seeking an MES Engineer with a strong testing mindset and hands-on Emerson Syncade experience to support a large pharmaceutical expansion in the Raleigh?Durham area. This role is... highly execution-focused and ideal for someone who thrives in dynamic manufacturing environments, can quickly learn new processes, and excels at validating MES configurations, calculations, and workflows in support of tech transfer and paperless manufacturing initiatives.The engineer will play a key role in supporting Syncade MES configuration and testing across two drug substance manufacturing facilities, working closely with Automation, Manufacturing, Quality, CSV, and CQV teams to ensure systems are robust, compliant, and ready to support new products and downstream operations.Key ResponsibilitiesMES Configuration & Support?Support the design, configuration, and implementation of an Emerson Syncade Manufacturing Execution System to enable paperless manufacturing with full ERP/MES/DCS integration.?Implement and troubleshoot MES configuration changes across DeltaV DCS, DeltaV MES (Syncade), and a custom formula/parameter management system.?Debug configuration items and system behaviors within Syncade, ensuring issues are properly triaged to the correct teams and resolved without impacting manufacturing execution.?Migrate solution components between Syncade environments (e.g., development, test, and production).MES Testing & Validation (Primary Focus)?Translate functional and technical requirements into detailed MES test protocols.?Execute MES testing across a large volume of documents and system objects, including: oLibrary objectsoCalculations and parameter setupsoRecipes and workflowsoElectronic Batch Records (EBR)?Design and execute testing strategies for rapidly evolving or dynamically developed configurations and code.?Support infrastructure setup, software installation, recipe development, and User Acceptance Testing (UAT) in partnership with end users.?Support tech transfer activities by identifying gaps between source and target processes, particularly as global processes are transferred and localized (e.g., Denmark ? US).Manufacturing & Tech Transfer Support?Support technical runs and process execution for both established and new downstream manufacturing operations.?Troubleshoot MES-related issues during execution, identifying whether problems stem from process design, system configuration, or operational use.?Ensure MES workflows do not inadvertently constrain or embed inaccurate manufacturing processes during tech transfer or scale-up activities.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/.

Feb 26, 2026

Chelmsford, MA

|

Mechanical Engineering

|

Contract

|

$36 - $45 (hourly estimate)

{"JobID":499804,"JobType":["Contract"],"EmployerID":null,"Location":{"Latitude":-71.3647,"Longitude":42.6233,"Distance":null},"State":"Massachusetts","Zip":"01824","ReferenceID":"BOS-92d1e7bb-866e-4bb3-a4b9-d6f2badb072c","PostedDate":"\/Date(1772110579000)\/","Description":"Insight Global is seeking a Facilities Technician for one of their top semiconductor clients. This person will play a key role in maintaining the smooth and safe operation of all building systems, with a primary focus on heating, ventilation, and air conditioning (HVAC) equipment. This role is responsible for troubleshooting, repairing, and performing preventive maintenance on HVAC systems while also providing general facilities support across plumbing, electrical, carpentry, and daily operational tasks. The ideal candidate is a hands-on problem solver who can work both independently and collaboratively within a fast-paced environment.Key Responsibilities: HVAC Maintenance \u0026 RepairDiagnose, troubleshoot, and repair HVAC systems including chillers, boilers, air handlers, and rooftop units.Perform routine and seasonal preventive maintenance to ensure equipment reliability.Monitor HVAC system performance and recommend improvements or repairs as needed.General Facilities Support Assist with basic plumbing and electrical repairs (e.g., fixtures, switches, minor wiring tasks).Support modular furniture installs, moves, and repairs.Perform light carpentry work including fixing locks, doors, and minor structural components.Operational DutiesConduct facility rounds to check equipment status and overall building conditions.Respond to service tickets promptly and ensure accurate documentation of work performed.Use QR codes and digital tools to update equipment history, maintenance logs, and asset data.Follow all safety protocols, ensuring compliance with internal and regulatory standards.Pay for this position is $17-24/hr based on qualifications and years of experienceWe 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":"1st Shift Facilities Technician","City":"Chelmsford","ExpirationDate":null,"PriorityOrder":0,"Requirements":"- 5 years of experience- Proven HVAC experience in installation, maintenance, and troubleshooting.- Experience with basic plumbing and electrical systems.- Basic carpentry experience - Experience working on electrical systems - Experience with modular furniture- Ability to work both independently and as part of a cross-functional team.- Strong problem-solving skills and a customer-focused mindset.","Skills":"Safety certifications (e.g., OSHA 10, lockout/tagout) or previous safety training.Experience in lab environments or regulated industries such as pharmaceutical, semiconductor, or solar manufacturing.","Industry":"Mechanical 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":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 seeking a Facilities Technician for one of their top semiconductor clients. This person will play a key role in maintaining the smooth and safe operation of all building systems,... with a primary focus on heating, ventilation, and air conditioning (HVAC) equipment. This role is responsible for troubleshooting, repairing, and performing preventive maintenance on HVAC systems while also providing general facilities support across plumbing, electrical, carpentry, and daily operational tasks. The ideal candidate is a hands-on problem solver who can work both independently and collaboratively within a fast-paced environment.Key Responsibilities: HVAC Maintenance & RepairDiagnose, troubleshoot, and repair HVAC systems including chillers, boilers, air handlers, and rooftop units.Perform routine and seasonal preventive maintenance to ensure equipment reliability.Monitor HVAC system performance and recommend improvements or repairs as needed.General Facilities Support Assist with basic plumbing and electrical repairs (e.g., fixtures, switches, minor wiring tasks).Support modular furniture installs, moves, and repairs.Perform light carpentry work including fixing locks, doors, and minor structural components.Operational DutiesConduct facility rounds to check equipment status and overall building conditions.Respond to service tickets promptly and ensure accurate documentation of work performed.Use QR codes and digital tools to update equipment history, maintenance logs, and asset data.Follow all safety protocols, ensuring compliance with internal and regulatory standards.Pay for this position is $17-24/hr based on qualifications and years of experienceWe 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

Upper Merion, PA

|

Computer Engineering

|

Contract-to-perm

|

$28 - $35 (hourly estimate)

{"JobID":529418,"JobType":["Contract-to-perm"],"EmployerID":null,"Location":{"Latitude":-75.38,"Longitude":40.09,"Distance":null},"State":"Pennsylvania","Zip":"19406","ReferenceID":"PHL-36516715-3be2-469c-8de1-700f506fab45","PostedDate":"\/Date(1778602665000)\/","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 IT and Quality, and 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 IT and Quality, and 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/.

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

|

Contract-to-perm

|

$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/.

May 19, 2026

Raritan, NJ

|

Business Analysis

|

Contract

|

$30 - $37 (hourly estimate)

{"JobID":532060,"JobType":["Contract"],"EmployerID":null,"Location":{"Latitude":-74.639,"Longitude":40.5719,"Distance":null},"State":"New Jersey","Zip":"08869","ReferenceID":"NNJ-388b2999-e40c-458c-8a16-fdaa753b4d48","PostedDate":"\/Date(1779220992000)\/","Description":"We are seeking a highly analytical and detail-oriented Senior Analyst to support commercial contracting and payment operations for the DePuy business as part of ongoing Project Osprey activities. This role will serve as a critical backfill resource to manage current workload while supporting transition and stabilization efforts.The ideal candidate will operate as a strategic partner to business stakeholders, ensuring accuracy and integrity across complex contract-driven calculations, commercial payments, and rebate structures.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":"Business/Data Analyst","City":"Raritan","ExpirationDate":null,"PriorityOrder":0,"Requirements":"3-4 years of experience as a Payments Analyst, Business Data Analyst or related field Advanced Microsoft Excel proficiency, including:Pivot TablesXLOOKUP / advanced formulasData filtering and large dataset managementConditional formattingText to ColumnsData validationStrong analytical capability with proven experience performing data validation and financial calculationsExperience interpreting and working with commercial contracts and pricing structuresFamiliarity with rebates, chargebacks, administrative fees, and performance-based incentivesAbility to understand and apply complex calculation logic across multiple variables and compliance metrics","Skills":"Experience with Model N and/or SAPBackground in Managed Markets, MedTech, or pharmaceutical contracting environments","Industry":"Business Analysis","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":37.0000,"SalaryLow":29.6000,"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)\/"}

We are seeking a highly analytical and detail-oriented Senior Analyst to support commercial contracting and payment operations for the DePuy business as part of ongoing Project Osprey activities.... This role will serve as a critical backfill resource to manage current workload while supporting transition and stabilization efforts.The ideal candidate will operate as a strategic partner to business stakeholders, ensuring accuracy and integrity across complex contract-driven calculations, commercial payments, and rebate structures.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 12, 2026

Palo Alto, CA

|

Laboratory Technician

|

Perm

|

$28 - $47 (hourly estimate)

{"JobID":540587,"JobType":["Perm"],"EmployerID":null,"Location":{"Latitude":-122.18,"Longitude":37.37,"Distance":null},"State":"California","Zip":"94304","ReferenceID":"NNJ-c56f2659-13be-4279-a74d-14a6ce452725","PostedDate":"\/Date(1781280027000)\/","Description":"Insight Global is seeking a Lab Equipment Maintenance Technician to join a biotechnology R\u0026D hub in Palo Alto. This individual will support daily facility and laboratory operations, leveraging hands-on experience in plumbing, electrical systems, and general building maintenance. Responsibilities include using diagnostic tools such as multimeters, gas meters, and temperature and airflow meters to operate, troubleshoot, repair, and calibrate a wide range of laboratory equipment while ensuring all utilities function reliably. This role also involves installing, relocating, and safely handling equipment to support ongoing projects, coordinating with vendors for specialized repairs, and maintaining accurate documentation and work orders while providing clear, timely communication to internal customers.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":"Lab Equipment Maintenance Technician","City":"Palo Alto","ExpirationDate":null,"PriorityOrder":0,"Requirements":"- High School Diploma required; technical training or AA/AS in Facilities Maintenance, Mechanical Engineering Technology, or a related trade preferred. - Experience performing facilities maintenance in a laboratory environment, including coordinating with vendors or contractors for specialized repairs. - Hands-on experience with lab utility systems (compressed air, RO/DI water, natural gas, oxygen, nitrogen, gas detection) and installing soft/rigid tubing (1/8\"?1/2\"), along with supporting installation, maintenance, and relocation of lab equipment (e.g., incubator shakers, biosafety cabinets, centrifuges, -80?C freezers, refrigerators, environmental chambers, chillers, water circulators). - Solid working knowledge of AC/DC electrical systems, basic plumbing, refrigeration systems, and associated controls, with experience using diagnostic tools such as multimeters, gas meters, temperature, and airflow meters. - Ability to perform seismic bracing for lab and process equipment and safely operate material handling equipment (forklifts, pallet jacks, hydraulic dollies) in compliance with EH\u0026S standards. - Strong documentation and organizational skills, including maintaining accurate records and reporting using Excel and Microsoft Office; OSHA safety training and forklift/powered industrial truck certification preferred.","Skills":"- Experience within biotechnology, pharmaceutical, or laboratory environments. - Technical training or education from a local trade school.","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":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)\/"}

Insight Global is seeking a Lab Equipment Maintenance Technician to join a biotechnology R&D hub in Palo Alto. This individual will support daily facility and laboratory operations, leveraging... hands-on experience in plumbing, electrical systems, and general building maintenance. Responsibilities include using diagnostic tools such as multimeters, gas meters, and temperature and airflow meters to operate, troubleshoot, repair, and calibrate a wide range of laboratory equipment while ensuring all utilities function reliably. This role also involves installing, relocating, and safely handling equipment to support ongoing projects, coordinating with vendors for specialized repairs, and maintaining accurate documentation and work orders while providing clear, timely communication to internal customers.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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