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May 12, 2026

New Haven, CT

|

Paramedic/EMT

|

Contract

|

$39 - $49 (hourly estimate)

{"JobID":529247,"JobType":["Contract"],"EmployerID":null,"Location":{"Latitude":-72.9383,"Longitude":41.3255,"Distance":null},"State":"Connecticut","Zip":"06511","ReferenceID":"HNJ-0024fa41-685b-4b31-aade-1fe686b4575f","PostedDate":"\/Date(1778584533000)\/","Description":"A large pharmaceutical company is seeking a strong paramedic to join their team. On a day-to-day basis, the Paramedic will be primarily responsible for providing care to clinical patients and during inter-facility and emergency transports following departmental predetermined treatment protocols. The Paramedic plays a vital part in the clinical trials patient\u0027s care.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":"Evergreen Part Time Paramedic","City":"New Haven","ExpirationDate":null,"PriorityOrder":0,"Requirements":"Minimum of 2-3 years of 911 or critical care transport experience Nationally registered Paramedic certification ACLS Certified Experience with ECG?s, Vital Signs, Blood Draws, etc","Skills":"","Industry":"Paramedic/EMT","Country":"US","Division":"IGH","Office":null,"IsRemoteJob":false,"IsInternalJob":false,"ExtraValues":null,"__RecordIndex":0,"__OrdinalPosition":0,"__Timestamp":0,"Status":null,"ApplicantCount":0,"SubmittalCount":0,"ApplicationToHireRatio":0,"JobDuration":null,"SalaryHigh":49.0000,"SalaryLow":39.2000,"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)\/"}

A large pharmaceutical company is seeking a strong paramedic to join their team. On a day-to-day basis, the Paramedic will be primarily responsible for providing care to clinical patients and during... inter-facility and emergency transports following departmental predetermined treatment protocols. The Paramedic plays a vital part in the clinical trials patient's care.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 18, 2026

Upper Merion, PA

|

QA

|

Contract

|

$52 - $65 (hourly estimate)

{"JobID":520444,"JobType":["Contract"],"EmployerID":null,"Location":{"Latitude":-75.38,"Longitude":40.09,"Distance":null},"State":"Pennsylvania","Zip":"19406","ReferenceID":"PHL-a21e7820-6c94-4517-8287-bae7f6bd8e61","PostedDate":"\/Date(1776546113000)\/","Description":"One of our API Pharmaceutical Manufacturing clients is seeking a highly experienced GMP Microbiology Laboratory SOP Development Specialist to support the establishment and readiness of a GMP microbiology laboratory in King of Prussia, PA. This is a 3-month consulting role which is responsible for the development, authorship, and implementation of Standard Operating Procedures (SOPs) and associated documentation to ensure compliant laboratory operations aligned with current Good Manufacturing Practices (cGMP), quality standards, and regulatory expectations. The ideal candidate will have strong technical knowledge of microbiology laboratory operations and demonstrated experience writing clear, compliant SOPs for GMP-regulated environments. Key responsibilities include:- SOP \u0026 Documentation Development- Laboratory Setup \u0026 Readiness Support- Quality \u0026 Compliance Collaboration- Training SupportWe 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 Lab SOP Development Specialist","City":"Upper Merion","ExpirationDate":null,"PriorityOrder":0,"Requirements":"- Bachelor?s degree in Microbiology, Biology, Life Sciences, or a related scientific discipline.- Minimum of 5 years of experience in a GMP-regulated microbiology laboratory environment.- Demonstrated experience authoring and implementing SOPs within GMP/Quality Systems.- Strong working knowledge of microbiological testing methods and laboratory best practices.- Familiarity with regulatory expectations (FDA, EU GMP, USP, ISO as applicable).- Excellent technical writing, organizational, and communication skills.- Ability to work independently in a fast-paced lab setup environment.","Skills":"- Experience supporting new laboratory start-ups or facility expansions.- Background in QA, Quality Systems, or compliance-related roles.- Experience working as a consultant or contingent resource in regulated environments.- Familiarity with electronic document management systems (EDMS).","Industry":"QA","Country":"US","Division":"AF\u0026E","Office":null,"IsRemoteJob":false,"IsInternalJob":false,"ExtraValues":null,"__RecordIndex":0,"__OrdinalPosition":0,"__Timestamp":0,"Status":null,"ApplicantCount":0,"SubmittalCount":0,"ApplicationToHireRatio":0,"JobDuration":null,"SalaryHigh":65.0000,"SalaryLow":52.0000,"PayRateOvertime":0,"PayRateStraight":0,"Filled":0,"RemainingOpenings":0,"TotalOpenings":0,"Visa":null,"ClearanceType":null,"IsClearanceRequired":false,"IsHealthcare":false,"IsRemote":false,"EndClient":null,"JobCreatedDate":"\/Date(-62135578800000)\/","JobModifiedDate":"\/Date(-62135578800000)\/"}

One of our API Pharmaceutical Manufacturing clients is seeking a highly experienced GMP Microbiology Laboratory SOP Development Specialist to support the establishment and readiness of a GMP... microbiology laboratory in King of Prussia, PA. This is a 3-month consulting role which is responsible for the development, authorship, and implementation of Standard Operating Procedures (SOPs) and associated documentation to ensure compliant laboratory operations aligned with current Good Manufacturing Practices (cGMP), quality standards, and regulatory expectations. The ideal candidate will have strong technical knowledge of microbiology laboratory operations and demonstrated experience writing clear, compliant SOPs for GMP-regulated environments. Key responsibilities include:- SOP & Documentation Development- Laboratory Setup & Readiness Support- Quality & Compliance Collaboration- Training SupportWe 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 24, 2026

Lower Gwynedd, PA

|

Software Engineering

|

Contract

|

$20 - $25 (hourly estimate)

{"JobID":522942,"JobType":["Contract"],"EmployerID":null,"Location":{"Latitude":-75.22,"Longitude":40.15,"Distance":null},"State":"Pennsylvania","Zip":"19002","ReferenceID":"KPD-958ec3fa-966f-4642-8e9e-a7923d3604f2","PostedDate":"\/Date(1777042673000)\/","Description":"Insight Global is currently seeking a PowerBI Developer for a large pharmaceutical client. This person will be joining a team responsible for build, enhancement, and maintenance of PowerBI dashboards supporting business units. This person will take pre-defined requirements, check data sources, build out visuals, create mockups, views, complete calculations, and do UAT with end users to ensure delivery of requirements. This person should have extensive experience with PowerBI.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":"PowerBI Developer - INTL India","City":"Lower Gwynedd","ExpirationDate":null,"PriorityOrder":0,"Requirements":"-5+ years of experience in PowerBI dashboard development-Mock up, calculation, DAX development-SQL back-end -Customer facing experience","Skills":"","Industry":"Software Engineering","Country":"US","Division":"IT","Office":null,"IsRemoteJob":false,"IsInternalJob":false,"ExtraValues":null,"__RecordIndex":0,"__OrdinalPosition":0,"__Timestamp":0,"Status":null,"ApplicantCount":0,"SubmittalCount":0,"ApplicationToHireRatio":0,"JobDuration":null,"SalaryHigh":25.0000,"SalaryLow":20.0000,"PayRateOvertime":0,"PayRateStraight":0,"Filled":0,"RemainingOpenings":0,"TotalOpenings":0,"Visa":null,"ClearanceType":null,"IsClearanceRequired":false,"IsHealthcare":false,"IsRemote":false,"EndClient":null,"JobCreatedDate":"\/Date(-62135578800000)\/","JobModifiedDate":"\/Date(-62135578800000)\/"}

Insight Global is currently seeking a PowerBI Developer for a large pharmaceutical client. This person will be joining a team responsible for build, enhancement, and maintenance of PowerBI dashboards... supporting business units. This person will take pre-defined requirements, check data sources, build out visuals, create mockups, views, complete calculations, and do UAT with end users to ensure delivery of requirements. This person should have extensive experience with PowerBI.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

New York, NY

|

Pharmacist

|

Contract,Perm Possible

|

$52 - $65 (hourly estimate)

{"JobID":529240,"JobType":["Contract,Perm Possible"],"EmployerID":null,"Location":{"Latitude":-73.99,"Longitude":40.71,"Distance":null},"State":"New York","Zip":"10022","ReferenceID":"SFR-b1ba9293-e3b5-4a18-8998-93ee47c4c892","PostedDate":"\/Date(1778554039000)\/","Description":"We power the future of consumer healthcare. We started in 2016 with a vision to modernize healthcare. We provide the building blocks needed to launch and scale world-class healthcare experiences.With millions of prescriptions shipped and millions of patients served, we work with many of theworld?s largest healthcare organizations - including payers, providers, life sciences companies,and consumer health brands. And with new partners continually joining our mission, we aim tofurther shape the future of healthcare - one patient at a time.We?re so glad you?re here. Let?s build something great together.About the RoleThe Staff Pharmacist reports to the Pharmacist in Charge to support our Pharmacy Operationsteam. You will be responsible for assisting the Pharmacist in Charge in managing all PharmacyTechnicians and delivery personnel.As a Staff Pharmacist with Truepill, you will play a key role in managing Pharmacy Technicians anddelivery personnel, ensuring the delivery of high-quality pharmaceutical services, and maintainingregulatory compliance.Why You?ll Love Working at Truepill?? We put patients first ? We put patients first because their well-being is our priority.? We are curious ? We never settle for how it?s done today. We invent how it will be donetomorrow. Because we don?t just ask ?why??, we ask ?why not??.? We have impact with urgency ? We?re the spark that ignites positive change in healthcare.We create impact because we don?t anticipate; we innovate.? We lead with Integrity ? Leading with integrity is the foundation of trust. We always dowhat?s best for our people, our customers, and above all, our patients.? We hold customer confidentiality ? We put discretion \u0026 confidentiality at the heart ofevery relationship.You?re excited about this opportunity because?? You will help with oversight of all Pharmacy Technicians and delivery personnel.? You will maintain appropriate documentation for services rendered, including prescriptionrecords and patient profiles.? You?ll coordinate the provision of pharmaceutical services and the delivery of medicationsand products to patients.? You will ensure the security of legend drugs and adherence to regulatory standards.? You will participate in the quality assurance program to maintain and improve pharmacyoperations.? You will maintain patient confidentiality with medication profiles and sensitive information.? You?ll collaborate with cross-functional teams to support organizational goals andinitiatives.? Your daily duties will include patient consultations, prescription verification, and drugutilization reviewWe 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":"Pharmacist - Brooklyn, New York","City":"New York","ExpirationDate":null,"PriorityOrder":0,"Requirements":"? You have an active, clear, and unrestricted Pharmacist license within the state of New York.? You are a Registered Pharmacist in good standing with the Board of Pharmacy.? You have a Bachelor?s degree in Pharmacy or Pharm D degree.? You possess a minimum of 1 year of pharmacy experience, preferably in a clinical setting.? You have the ability and willingness to work at a computer screen for long periods ifneeded.? You have demonstrated excellent leadership and organizational skills to effectively managepharmacy operations.? You display a commitment to patient-centered care and adherence to ethical standards.? You have strong communication skills and the ability to work collaboratively in a teamenvironment.? You\u0027re able to work onsite in the Brooklyn, NY office for one of the below shift schedules:?Sunday-Wednesday: 9 p.m.?7:30 a.m. ET?Monday-Friday: 7:30 a.m.?4 p.m. ET?Tuesday-Friday: 7:30 a.m.?4 p.m. ET; Saturday: 8 a.m.?4:30 p.m. ET","Skills":"","Industry":"Pharmacist","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":65.0000,"SalaryLow":52.0000,"PayRateOvertime":0,"PayRateStraight":0,"Filled":0,"RemainingOpenings":0,"TotalOpenings":0,"Visa":null,"ClearanceType":null,"IsClearanceRequired":false,"IsHealthcare":false,"IsRemote":false,"EndClient":null,"JobCreatedDate":"\/Date(-62135578800000)\/","JobModifiedDate":"\/Date(-62135578800000)\/"}

We power the future of consumer healthcare. We started in 2016 with a vision to modernize healthcare. We provide the building blocks needed to launch and scale world-class healthcare experiences.With... millions of prescriptions shipped and millions of patients served, we work with many of theworld?s largest healthcare organizations - including payers, providers, life sciences companies,and consumer health brands. And with new partners continually joining our mission, we aim tofurther shape the future of healthcare - one patient at a time.We?re so glad you?re here. Let?s build something great together.About the RoleThe Staff Pharmacist reports to the Pharmacist in Charge to support our Pharmacy Operationsteam. You will be responsible for assisting the Pharmacist in Charge in managing all PharmacyTechnicians and delivery personnel.As a Staff Pharmacist with Truepill, you will play a key role in managing Pharmacy Technicians anddelivery personnel, ensuring the delivery of high-quality pharmaceutical services, and maintainingregulatory compliance.Why You?ll Love Working at Truepill?? We put patients first ? We put patients first because their well-being is our priority.? We are curious ? We never settle for how it?s done today. We invent how it will be donetomorrow. Because we don?t just ask ?why??, we ask ?why not??.? We have impact with urgency ? We?re the spark that ignites positive change in healthcare.We create impact because we don?t anticipate; we innovate.? We lead with Integrity ? Leading with integrity is the foundation of trust. We always dowhat?s best for our people, our customers, and above all, our patients.? We hold customer confidentiality ? We put discretion & confidentiality at the heart ofevery relationship.You?re excited about this opportunity because?? You will help with oversight of all Pharmacy Technicians and delivery personnel.? You will maintain appropriate documentation for services rendered, including prescriptionrecords and patient profiles.? You?ll coordinate the provision of pharmaceutical services and the delivery of medicationsand products to patients.? You will ensure the security of legend drugs and adherence to regulatory standards.? You will participate in the quality assurance program to maintain and improve pharmacyoperations.? You will maintain patient confidentiality with medication profiles and sensitive information.? You?ll collaborate with cross-functional teams to support organizational goals andinitiatives.? Your daily duties will include patient consultations, prescription verification, and drugutilization reviewWe are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com.To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/.

Mar 10, 2026

Parsippany, NJ

|

Engineering (Non IT)

|

Contract

|

$50 - $62 (hourly estimate)

{"JobID":504617,"JobType":["Contract"],"EmployerID":null,"Location":{"Latitude":-74.4061,"Longitude":40.862,"Distance":null},"State":"New Jersey","Zip":"07054","ReferenceID":"NNJ-02b6a38a-cda8-4591-a2da-ccbc81684b99","PostedDate":"\/Date(1773153089000)\/","Description":"Seeking a mid- to senior-level Validation Engineer to support commissioning and qualification activities within a pharmaceutical manufacturing environment. The role will be responsible for generating and executing IQ, OQ, and PQ protocols for equipment, utilities, and packaging systems, ensuring compliance with cGMP and regulatory expectations. The candidate should be comfortable working both independently and collaboratively, with the ability to lead validation activities and drive projects to completion.We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com.To learn more about how we collect, keep, and process your private information, please review Insight Global\u0027s Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/.","Title":"Senior Validation Engineer","City":"Parsippany","ExpirationDate":null,"PriorityOrder":0,"Requirements":"? Author and execute Commissioning, Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) protocols.? Support qualification of process equipment, packaging lines, laboratory equipment, utilities, and facility systems.? Perform temperature mapping studies for controlled temperature equipment and storage areas.? Support cleanroom and room qualification activities.? Execute or support media fills (aseptic process simulations) and smoke studies.? Support Environmental Monitoring (EM) studies.? Investigate and document deviations encountered during qualification activities.? Prepare validation documentation and summary reports.Work cross-functionally with internal teams (i.e., Engineering, Quality, Manufacturing, Supply Chain, and Validation) to support qualification activities and ensure project timelines are met.","Skills":"","Industry":"Engineering (Non IT)","Country":"US","Division":"AF\u0026E","Office":null,"IsRemoteJob":false,"IsInternalJob":false,"ExtraValues":null,"__RecordIndex":0,"__OrdinalPosition":0,"__Timestamp":0,"Status":null,"ApplicantCount":0,"SubmittalCount":0,"ApplicationToHireRatio":0,"JobDuration":null,"SalaryHigh":62.0000,"SalaryLow":49.6000,"PayRateOvertime":0,"PayRateStraight":0,"Filled":0,"RemainingOpenings":0,"TotalOpenings":0,"Visa":null,"ClearanceType":null,"IsClearanceRequired":false,"IsHealthcare":false,"IsRemote":false,"EndClient":null,"JobCreatedDate":"\/Date(-62135578800000)\/","JobModifiedDate":"\/Date(-62135578800000)\/"}

Seeking a mid- to senior-level Validation Engineer to support commissioning and qualification activities within a pharmaceutical manufacturing environment. The role will be responsible for generating... and executing IQ, OQ, and PQ protocols for equipment, utilities, and packaging systems, ensuring compliance with cGMP and regulatory expectations. The candidate should be comfortable working both independently and collaboratively, with the ability to lead validation activities and drive projects to completion.We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com.To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/.

Apr 15, 2026

East Greenbush, NY

|

Chemical Engineering

|

Contract

|

$59 - $74 (hourly estimate)

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Insight Global is seeking a QA to join one of our largest pharmaceutical clients 5x/week onsite in Rensselaer, NY. This individual will be joining the Cleanroom team within the Facilities Engineering... space assisting in lifecycle of reports being processed by the QA team. They will be responsible for managing reports from vendors, executing report reviews, adjusting QA comments, and pushing through to the next step in the report lifecycle. They will be expected to perform a high-level review through QA, identify any Gx issues, and ensuring acceptance criteria is accurate. This will be a mainly individual contributor but will be expected to work cross functionally with QA for oversight from the team when needed.We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com.To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/.

Aug 27, 2025

Hopewell Township, NJ

|

Data Warehousing

|

Contract

|

$31 - $39 (hourly estimate)

{"JobID":438112,"JobType":["Contract"],"EmployerID":null,"Location":{"Latitude":-74.8562,"Longitude":40.2985,"Distance":null},"State":"New Jersey","Zip":"08560","ReferenceID":"NNJ-381c1529-8d47-437b-b95e-b3506da33fe2","PostedDate":"\/Date(1756310169000)\/","Description":"Our top Pharmaceutical client is seeking a Documentation and Validation specialist to join their External Call Center team within their Patient Experience Org, The are currently insourcing their call center capabilities for supporting end-to-end patient journey\u0027s and are in need for a resource with IVR and Contact Center knowledge to spearhead documentation and validation of processes. The ideal resource will have experience with Salesforce Service Cloud, Visio, PPT, and other process documentation tools to document workflows and validation.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":"IVR Validation Specialist","City":"Hopewell Township","ExpirationDate":null,"PriorityOrder":0,"Requirements":"5+ years\u0027 in contact center supportExtensive documentation and validaiton skillsknowledge of CRM and Patient Health Information data requirements","Skills":"","Industry":"Data Warehousing","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":39.0000,"SalaryLow":31.2000,"PayRateOvertime":0,"PayRateStraight":0,"Filled":0,"RemainingOpenings":0,"TotalOpenings":0,"Visa":null,"ClearanceType":null,"IsClearanceRequired":false,"IsHealthcare":false,"IsRemote":false,"EndClient":null,"JobCreatedDate":"\/Date(-62135578800000)\/","JobModifiedDate":"\/Date(-62135578800000)\/"}

Our top Pharmaceutical client is seeking a Documentation and Validation specialist to join their External Call Center team within their Patient Experience Org, The are currently insourcing their call... center capabilities for supporting end-to-end patient journey's and are in need for a resource with IVR and Contact Center knowledge to spearhead documentation and validation of processes. The ideal resource will have experience with Salesforce Service Cloud, Visio, PPT, and other process documentation tools to document workflows and validation.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

Clayton, NC

|

Engineering (Non IT)

|

Contract

|

$52 - $65 (hourly estimate)

{"JobID":529574,"JobType":["Contract"],"EmployerID":null,"Location":{"Latitude":-78.45,"Longitude":35.64,"Distance":null},"State":"North Carolina","Zip":"27520","ReferenceID":"RAL-63cff904-253f-4e79-a9ca-f9dddd0588a7","PostedDate":"\/Date(1778614629000)\/","Description":"Insight Global is seeking an IT Automation Engineer for a pharmaceutical client in the Raleigh area. The IT Automation Engineer will support the Fill Finish Expansion Project at their greenfield facility. These engineers will support the deployment, integration, testing, and troubleshooting of automated assembly and packaging equipment within Finished Products buildings. The role is hands-on and project-focused, supporting OEM equipment, PLC/SCADA systems, MES, serialization, and IT/OT integration in a highly regulated GMP environment.We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com.To learn more about how we collect, keep, and process your private information, please review Insight Global\u0027s Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/.","Title":"IT Automation Engineer","City":"Clayton","ExpirationDate":null,"PriorityOrder":0,"Requirements":"Strong hands-on experience supporting automation systems in manufacturingExperience working with OEM packaging and assembly equipmentPLC experience with one or more of the following:Schneider, B\u0026R, Allen-Bradley ControlLogix, SiemensExperience with SCADA systems (FactoryTalk preferred)Familiarity with MES (PAS-X) and serialization systems (Uhlmann Track \u0026 Trace)Experience executing SAT / IV / OV testingUnderstanding of IT/OT integration in industrial environmentsExperience working in regulated industries (pharma, biotech, medical device preferred)","Skills":"Experience with SQL Server, Aveva PI,Vision system experience Networking fundamentals in industrial environmentsCybersecurity awareness specific to OT systemsGreenfield or large CAPEX project experience","Industry":"Engineering (Non IT)","Country":"US","Division":"AF\u0026E","Office":null,"IsRemoteJob":false,"IsInternalJob":false,"ExtraValues":null,"__RecordIndex":0,"__OrdinalPosition":0,"__Timestamp":0,"Status":null,"ApplicantCount":0,"SubmittalCount":0,"ApplicationToHireRatio":0,"JobDuration":null,"SalaryHigh":65.0000,"SalaryLow":52.0000,"PayRateOvertime":0,"PayRateStraight":0,"Filled":0,"RemainingOpenings":0,"TotalOpenings":0,"Visa":null,"ClearanceType":null,"IsClearanceRequired":false,"IsHealthcare":false,"IsRemote":false,"EndClient":null,"JobCreatedDate":"\/Date(-62135578800000)\/","JobModifiedDate":"\/Date(-62135578800000)\/"}

Insight Global is seeking an IT Automation Engineer for a pharmaceutical client in the Raleigh area. The IT Automation Engineer will support the Fill Finish Expansion Project at their greenfield... facility. These engineers will support the deployment, integration, testing, and troubleshooting of automated assembly and packaging equipment within Finished Products buildings. The role is hands-on and project-focused, supporting OEM equipment, PLC/SCADA systems, MES, serialization, and IT/OT integration in a highly regulated GMP environment.We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com.To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/.

May 15, 2026

Lower Gwynedd, PA

|

Project Manager

|

Contract

|

$44 - $55 (hourly estimate)

{"JobID":530973,"JobType":["Contract"],"EmployerID":null,"Location":{"Latitude":-75.22,"Longitude":40.15,"Distance":null},"State":"Pennsylvania","Zip":"19002","ReferenceID":"KPD-c46b3212-9ada-4119-804c-65b00bc55df2","PostedDate":"\/Date(1778871521000)\/","Description":"Insight Global is currently seeking a Business Analyst/Project Manager for a large pharmaceutical client. This person will be joining a technology group responsible for build, implementation, enhancement, and support of innovative technology solutions including AI/ML. This person will join a project focused on POC creation for a new technology. They will be responsible for gathering requirements, creating documentation, and updating of JIRA board in response to completion of items/re-prioritization. They will also be responsible for PM related responsibilities including project plan tracking, identification of dependencies/risks/timeline changes, and internal technical team/external vendor coordination. This person should have extensive experience in hybrid BA/PM roles focused on technology projects.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 Analyst - Pharma R\u0026D","City":"Lower Gwynedd","ExpirationDate":null,"PriorityOrder":0,"Requirements":"Skillset-5+ years of experience in a BA/PM role in an enterprise environment-Requirements gathering, agile documentation, scrum ceremony leadership, and build/test plan creation-Project plan creation, management, and internal/external technical team coordination-Kubernetes and AWS related project experience","Skills":"Plusses-Pharma R\u0026D experience-AI/ML project work","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":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)\/"}

Insight Global is currently seeking a Business Analyst/Project Manager for a large pharmaceutical client. This person will be joining a technology group responsible for build, implementation,... enhancement, and support of innovative technology solutions including AI/ML. This person will join a project focused on POC creation for a new technology. They will be responsible for gathering requirements, creating documentation, and updating of JIRA board in response to completion of items/re-prioritization. They will also be responsible for PM related responsibilities including project plan tracking, identification of dependencies/risks/timeline changes, and internal technical team/external vendor coordination. This person should have extensive experience in hybrid BA/PM roles focused on technology projects.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, 2024

Boston, MA

|

Biomedical Engineering

|

Contract

|

$62 - $78 (hourly estimate)

{"JobID":355529,"JobType":["Contract"],"EmployerID":null,"Location":{"Latitude":-71.0159818181818,"Longitude":42.3511454545455,"Distance":null},"State":"Massachusetts","Zip":"02210","ReferenceID":"BOS-b69ec0b3-e86c-4652-9fba-e237daca48e5","PostedDate":"\/Date(1715004860000)\/","Description":"Insight Global is looking for a QC Analytical Investigator to sit on-site at a brand new facility in the beautiful Seaport district of Boston supporting one of our top pharmaceutical clients. This is a first shift role, on-site Monday through Friday. This position will be supporting the growing technical services team in their risk assessment efforts. This role will be responsible for conducting RCA, assessing impacts, and developing CAPAs to ensure efficient and effective processes across the cell and gene therapy organization. A strong candidate for this role will have a strong background in QC Analytical risk assessments, in GMP environment, leading, writing and reviewing deviations and investigations. Th This person will need to be comfortable managing several projects simultaneously with various stakeholders, maintaining a project management mind-set. Additionally, they should be comfortable working independently and confidently managing decisions on their own. This is an amazing opportunity for a mid-level professional to get their foot in the door at a fast-paced and high growth company and take the next step in their career!We are a company committed to creating inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity employer that believes everyone matters. Qualified candidates will receive consideration for employment opportunities without regard to race, religion, sex, age, marital status, national origin, sexual orientation, citizenship status, disability, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to Human Resources Request Form. The EEOC \"Know Your Rights\" Poster is available here. To learn more about how we collect, keep, and process your private information, please review Insight Global\u0027s Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/ .","Title":"QC Analytical Investigator","City":"Boston","ExpirationDate":null,"PriorityOrder":0,"Requirements":"? 3+ years of QC Analytical risk assessment management experience in a GMP environment? Project management experience, comfortable managing multiple stakeholder relationships? Strong technical writer with previous experience authoring, reviewing and editing risk assessment, CAPA and deviation documents? Effective communicator with ability to influence a group of people? Previous experience with an eQMS system, ideally VeevaBachelor\u0027s Degree","Skills":"","Industry":"Biomedical 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":78.0000,"SalaryLow":62.4000,"PayRateOvertime":0,"PayRateStraight":0,"Filled":0,"RemainingOpenings":0,"TotalOpenings":0,"Visa":null,"ClearanceType":null,"IsClearanceRequired":false,"IsHealthcare":false,"IsRemote":false,"EndClient":null,"JobCreatedDate":"\/Date(-62135578800000)\/","JobModifiedDate":"\/Date(-62135578800000)\/"}

Insight Global is looking for a QC Analytical Investigator to sit on-site at a brand new facility in the beautiful Seaport district of Boston supporting one of our top pharmaceutical clients. This is... a first shift role, on-site Monday through Friday. This position will be supporting the growing technical services team in their risk assessment efforts. This role will be responsible for conducting RCA, assessing impacts, and developing CAPAs to ensure efficient and effective processes across the cell and gene therapy organization. A strong candidate for this role will have a strong background in QC Analytical risk assessments, in GMP environment, leading, writing and reviewing deviations and investigations. Th This person will need to be comfortable managing several projects simultaneously with various stakeholders, maintaining a project management mind-set. Additionally, they should be comfortable working independently and confidently managing decisions on their own. This is an amazing opportunity for a mid-level professional to get their foot in the door at a fast-paced and high growth company and take the next step in their career!We are a company committed to creating inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity employer that believes everyone matters. Qualified candidates will receive consideration for employment opportunities without regard to race, religion, sex, age, marital status, national origin, sexual orientation, citizenship status, disability, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to Human Resources Request Form. The EEOC "Know Your Rights" Poster is available here. To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/ .

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