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Apr 30, 2024

Rahway, NJ

|

Software Engineering

|

Contract

|

$48 - $72 (hourly estimate)

{"JobID":354377,"JobType":["Contract"],"EmployerID":null,"Location":{"Latitude":-74.2654,"Longitude":40.6163363636364,"Distance":null},"State":"New Jersey","Zip":"07065","ReferenceID":"NNJ-701079","PostedDate":"\/Date(1714472059000)\/","Description":"Insight Global is seeking a software engineer to support a pharmacetucial client . This Software Engineer will design, analyze, and archive high-throughput experiments (HTE). The successful applicant will be primarily responsible for expanding the functionality of existing software packages (see below for links), creating web-based graphical interfaces for scientists, and writing code to extract binary data from scientific instruments. This position is a unique opportunity to learn and apply computer science skills to mission-critical problems in the pharmaceutical sector.Day-to-day work will include writing Python code for the PyPlate scripting backend, JS or other frontend code for the PyPlate graphical frontend, and Python/C code for the Rainbow backend. The successful applicant will be expected to adhere to generally accepted industry practices for code hygiene: clear documentation, rigorous tests, version control, etc.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":"Pharmaceutical Software Engineer - Remote","City":"Rahway","ExpirationDate":null,"PriorityOrder":0,"Requirements":"Previous experience in the pharmaceutical industry supporting research organizationsA strong understanding of the fundamentals of computer science, software engineering, and binary storage.Deep expertise in Python and API design. Demonstrated track-record of effective use of documentation, version control, continuous integration, and code testing tools.Ability to write C-based extensions or other numerically optimized code for Python","Skills":"Understanding of chemistry and the physical sciences, such as how to perform basic stoichiometric calculations, create recipes for pH buffers, or interpret data from chromatography and mass spectrometric experimentsFamiliarity with Streamlit, Dash, or similar packages for low-code front-end prototyping; or, better yet, knowledge of JS/CSS and related frameworks for front-end web development","Industry":"Software 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":72.0000,"SalaryLow":48.0000,"PayRateOvertime":0,"PayRateStraight":0,"Filled":0,"RemainingOpenings":0,"TotalOpenings":0,"Visa":null,"ClearanceType":null,"IsClearanceRequired":false,"IsHealthcare":false,"IsRemote":false,"EndClient":null,"JobCreatedDate":"\/Date(-62135578800000)\/","JobModifiedDate":"\/Date(-62135578800000)\/"}

Insight Global is seeking a software engineer to support a pharmacetucial client . This Software Engineer will design, analyze, and archive high-throughput experiments (HTE). The successful... applicant will be primarily responsible for expanding the functionality of existing software packages (see below for links), creating web-based graphical interfaces for scientists, and writing code to extract binary data from scientific instruments. This position is a unique opportunity to learn and apply computer science skills to mission-critical problems in the pharmaceutical sector.Day-to-day work will include writing Python code for the PyPlate scripting backend, JS or other frontend code for the PyPlate graphical frontend, and Python/C code for the Rainbow backend. The successful applicant will be expected to adhere to generally accepted industry practices for code hygiene: clear documentation, rigorous tests, version control, etc.We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com.To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/ .

Mar 06, 2024

Parsippany, NJ

|

Business Analysis

|

Perm

|

$66k - $98k (estimate)

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Insight Global is looking for a full-time maintenance planner scheduler to join one of our pharmaceutical clients. This individual will devise plans and programs for routine preventative maintenance... and schedule events around the production facility. This individual will use software's such as Excel, MS projects, CMMS and smart sheets to build schedules. This individual will also monitor spare parts inventory to ensure availability of required parts. This individual will be interfacing with cross functional teams daily. We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com.To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/ .

Apr 09, 2024

West Point, PA

|

Engineering (Non IT)

|

Contract,Perm Possible

|

$31 - $47 (hourly estimate)

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Their main responsibility is coordinating QNs (Quality Notifications), identify point of occurrence, investigate root cause, and evaluate product impact by using DM tools to close incidents and investigations by assigned due date. Examples of incidents could include: incorrect build, leak in the area, not documentation correctly, etc. They will be working directly with the shop floor to roll out these changes. This is a hybrid position, 4 days onsite \u0026 1 day WFH. *Manage investigations from notification through closure meeting timelines to ensure key compliance and customer due dates are met; escalating any potential delays and develop remediation plans when possible. *Support and/or execution of process improvement projects and complex manufacturing investigations. *Completes projects to improve the performance of our processes, including investigation Corrective / Preventative Actions (CAPAs), projects aimed at improving \"Right First Time\" performance or preventing / reducing deviations. Leads and/or works as a team member on complete manufacturing investigations, process improvement and/or validation projects. *Examines an issue from diverse perspectives (safety, compliance, automation, equipment, process, and people) in order to best understand and resolve the root cause. *Provides on the floor assistance of operational and technical issues on the shop floor. *Designs and conducts experimental protocols as needed using the Technical Operations lab facilities and/or production equipment at full scale. *Authors and updates technical and manufacturing documents necessary for engineering studies or process demonstrations. *Completes projects to improve the performance of our processes, including investigation Corrective / Preventative Actions (CAPAs), projects aimed at improving \"Right First Time\" performance or preventing / reducing deviations. *Promote team safety, environmental, and compliance objectives.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":"Deviation Management Specialist","City":"West Point","ExpirationDate":null,"PriorityOrder":0,"Requirements":"*B.S. Degree in Engineering or Sciences. *Technical Writing \u0026 Authoring Investigations experience *Root Cause Analysis experience *Minimum two years\u0027 experience in GMP pharmaceutical manufacturing technical support of GMP manufacturing operations *Experience working with manufacturing equipment, such as autoclaves, fit testers, washers, dry heat ovens, sonicators *Experience in deviation management and/or change control and /or equipment or project support role. *Highly developed communication, leadership and teamwork skills. *Ability to manage projects/work to schedule/deadlines.","Skills":"*Background in biologics, vaccine, or bulk sterile manufacturing facilities *Deviation Management Investigator including Root Cause Certification. *SAP","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":46.8000,"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)\/"}

One of our large pharmaceutical clients is actively seeking a Deviation Management Specialist to join the sterile supply incoming materials team located in West Point, PA. They will be responsible... for ensuring that deviations are thoroughly investigated, risks are managed, and corrective actions are taken to maintain equipment quality & compliance in the pharmaceutical industry. This person needs to have experience authoring investigations & incidents for pharmaceutical manufacturing equipment. Their main responsibility is coordinating QNs (Quality Notifications), identify point of occurrence, investigate root cause, and evaluate product impact by using DM tools to close incidents and investigations by assigned due date. Examples of incidents could include: incorrect build, leak in the area, not documentation correctly, etc. They will be working directly with the shop floor to roll out these changes. This is a hybrid position, 4 days onsite & 1 day WFH. *Manage investigations from notification through closure meeting timelines to ensure key compliance and customer due dates are met; escalating any potential delays and develop remediation plans when possible. *Support and/or execution of process improvement projects and complex manufacturing investigations. *Completes projects to improve the performance of our processes, including investigation Corrective / Preventative Actions (CAPAs), projects aimed at improving "Right First Time" performance or preventing / reducing deviations. Leads and/or works as a team member on complete manufacturing investigations, process improvement and/or validation projects. *Examines an issue from diverse perspectives (safety, compliance, automation, equipment, process, and people) in order to best understand and resolve the root cause. *Provides on the floor assistance of operational and technical issues on the shop floor. *Designs and conducts experimental protocols as needed using the Technical Operations lab facilities and/or production equipment at full scale. *Authors and updates technical and manufacturing documents necessary for engineering studies or process demonstrations. *Completes projects to improve the performance of our processes, including investigation Corrective / Preventative Actions (CAPAs), projects aimed at improving "Right First Time" performance or preventing / reducing deviations. *Promote team safety, environmental, and compliance objectives.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 11, 2024

Somerville, NJ

|

Technical Writer

|

Contract

|

$28 - $42 (hourly estimate)

{"JobID":350735,"JobType":["Contract"],"EmployerID":null,"Location":{"Latitude":-74.6545454545455,"Longitude":40.5499727272727,"Distance":null},"State":"New Jersey","Zip":"08876","ReferenceID":"NNJ-696768","PostedDate":"\/Date(1712837819000)\/","Description":"One of our large pharmaceutical and medical device clients is looking for a doc management specialist strong in technical writing to join a project team. This individual will be responsible for writing quality procedures, following SOPs, assisting in internal \u0026 regulatory audits, and overall management of regulatory healthcare procedural documents. This role will involve conducting research to ensure content is accurate and gathering and organizing information in various functional areas. This role requires an on-site presence in New Brunswick, NJ 4x a week.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":"Document Management Specialist","City":"Somerville","ExpirationDate":null,"PriorityOrder":0,"Requirements":"-5+ years\u0027 experience with technical writing-Experience within pharmaceutical or medical device industries-3+ years\u0027 experience with regulatory document management -Knowledge of internal or regulatory audits-Experience following SOPs-Bachelor\u0027s Degree","Skills":"-Experience utilizing a Quality Management System-Experience supporting LMS programs","Industry":"Technical Writer","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":42.0000,"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 pharmaceutical and medical device clients is looking for a doc management specialist strong in technical writing to join a project team. This individual will be responsible for... writing quality procedures, following SOPs, assisting in internal & regulatory audits, and overall management of regulatory healthcare procedural documents. This role will involve conducting research to ensure content is accurate and gathering and organizing information in various functional areas. This role requires an on-site presence in New Brunswick, NJ 4x a week.We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com.To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/ .

Mar 26, 2024

Parsippany, NJ

|

QA

|

Perm

|

$89k - $133k (estimate)

{"JobID":347463,"JobType":["Perm"],"EmployerID":null,"Location":{"Latitude":-74.3926454545454,"Longitude":40.8764545454545,"Distance":null},"State":"New Jersey","Zip":"07054","ReferenceID":"NNJ-692899","PostedDate":"\/Date(1711455262000)\/","Description":"Insight Global is seeking an experienced Sr. Validation Specialist to join one of our large pharmaceutical clients for a full-time position. This position will be 5 days a week onsite, in Parsippany, NJ. This individual will play a crucial role in ensuring quality and compliance of pharmaceutical equipment. The ideal individual will have experience developing validation protocols for various process equipment and systems. This individual will have to execute validation test according to established protocols (IQ, OQ,PQ). We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com.To learn more about how we collect, keep, and process your private information, please review Insight Global\u0027s Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/ .","Title":"Sr. Validation Specialist","City":"Parsippany","ExpirationDate":null,"PriorityOrder":0,"Requirements":"5+ years Validation specialist or engineer within Pharma or Biopharma. Experience executing and writing test protocols Qualification (IQ), Operational Qualification (OQ), Performance Qualification (PQ). Comprehensive knowledge of production processes. Experience with Trackwise or Veeva.","Skills":"Knowledge of Capa and Deviations.","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":133260.0000,"SalaryLow":88840.0000,"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 experienced Sr. Validation Specialist to join one of our large pharmaceutical clients for a full-time position. This position will be 5 days a week onsite, in Parsippany,... NJ. This individual will play a crucial role in ensuring quality and compliance of pharmaceutical equipment. The ideal individual will have experience developing validation protocols for various process equipment and systems. This individual will have to execute validation test according to established protocols (IQ, OQ,PQ). We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com.To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/ .

Mar 22, 2024

West Point, PA

|

Engineering (Non IT)

|

Contract,Perm Possible

|

$43 - $65 (hourly estimate)

{"JobID":346872,"JobType":["Contract,Perm Possible"],"EmployerID":null,"Location":{"Latitude":-75.2728181818182,"Longitude":40.212,"Distance":null},"State":"Pennsylvania","Zip":"19486","ReferenceID":"PHL-692132","PostedDate":"\/Date(1711098842000)\/","Description":"One of our large pharmaceutical clients located in West Point, PA is seeking a Process Engineer to join their team. This team is responsible for setting up an entire new manufacturing operation for syringe and vial filing. They oversee design, construction and process qualification and will be apart of the start up/transfer of a state of the art pharma drug manufacturing facility. The equipment they will be working on are Fermenters, Filling Lines, Tanks, Formulations, Syringe filling , CIP and SIPS. Other responsibilities:Update SOPs/ complete bath record reviewsWriting protocols Use change management system to update tasks that need mappingRoot cause analysis for manufacturing system deviationsHeavy use of MS Project for building projects plans/schedulesWe 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":"Process Engineer","City":"West Point","ExpirationDate":null,"PriorityOrder":0,"Requirements":"Bachelors in Engineering5 years experience within the pharmaceutical manufacturing industry Project management experience - PMP certification will be significantMicrosoft project / schedule management experienceExperience with tracking project schedules Facility equipment startup experienceIQ-OQ-PQ hands on execution","Skills":"CIP-SIP execution experience is a plusPMP certification","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":64.8000,"SalaryLow":43.2000,"PayRateOvertime":0,"PayRateStraight":0,"Filled":0,"RemainingOpenings":0,"TotalOpenings":0,"Visa":null,"ClearanceType":null,"IsClearanceRequired":false,"IsHealthcare":false,"IsRemote":false,"EndClient":null,"JobCreatedDate":"\/Date(-62135578800000)\/","JobModifiedDate":"\/Date(-62135578800000)\/"}

One of our large pharmaceutical clients located in West Point, PA is seeking a Process Engineer to join their team. This team is responsible for setting up an entire new manufacturing operation for... syringe and vial filing. They oversee design, construction and process qualification and will be apart of the start up/transfer of a state of the art pharma drug manufacturing facility. The equipment they will be working on are Fermenters, Filling Lines, Tanks, Formulations, Syringe filling , CIP and SIPS. Other responsibilities:Update SOPs/ complete bath record reviewsWriting protocols Use change management system to update tasks that need mappingRoot cause analysis for manufacturing system deviationsHeavy use of MS Project for building projects plans/schedulesWe 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 23, 2024

Rensselaer, NY

|

Administrative Assistant

|

Contract

|

$29 - $43 (hourly estimate)

{"JobID":353017,"JobType":["Contract"],"EmployerID":null,"Location":{"Latitude":-73.7237272727273,"Longitude":42.6496363636364,"Distance":null},"State":"New York","Zip":"12144","ReferenceID":"NYC-699450","PostedDate":"\/Date(1713881776000)\/","Description":"A large pharmaceutical client is looking for a Technical Writer to join the team in Albany, NY. This candidate will be developing reports specific to quality control. They must have excellent writing skills and be able to read physical documents and translate them into detailed reports. Attention to detail and previous technical writing experience is crucial to be successful in this role. 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":"Technical Writer","City":"Rensselaer","ExpirationDate":null,"PriorityOrder":0,"Requirements":"-1+ year of technical writing experience-Strong attention to detail-Ability to read physical documents and translate them into detailed reports","Skills":"-Experience working in highly regulated environment/GxP/GDP/GMP experience -Experience working in the pharmaceutical industry","Industry":"Administrative Assistant","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":42.9000,"SalaryLow":28.6000,"PayRateOvertime":0,"PayRateStraight":0,"Filled":0,"RemainingOpenings":0,"TotalOpenings":0,"Visa":null,"ClearanceType":null,"IsClearanceRequired":false,"IsHealthcare":false,"IsRemote":false,"EndClient":null,"JobCreatedDate":"\/Date(-62135578800000)\/","JobModifiedDate":"\/Date(-62135578800000)\/"}

A large pharmaceutical client is looking for a Technical Writer to join the team in Albany, NY. This candidate will be developing reports specific to quality control. They must have excellent writing... skills and be able to read physical documents and translate them into detailed reports. Attention to detail and previous technical writing experience is crucial to be successful in this role. We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com.To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/ .

Mar 26, 2024

Parsippany, NJ

|

QA

|

Perm

|

$77k - $115k (estimate)

{"JobID":347465,"JobType":["Perm"],"EmployerID":null,"Location":{"Latitude":-74.3854636363636,"Longitude":40.8765454545455,"Distance":null},"State":"New Jersey","Zip":"07054","ReferenceID":"NNJ-692903","PostedDate":"\/Date(1711455262000)\/","Description":"Insight Global is seeking an experienced Sr. Validation Specialist to join one of our large pharmaceutical clients for a full-time position. This position will be 5 days a week onsite, in Parsippany, NJ. This individual will play a crucial role in ensuring quality and compliance of pharmaceutical equipment. The ideal individual will have experience with the execution of validation protocols for various process equipment and systems. This individual will have to assist in the execution of validation test according to established protocols (IQ, OQ, PQ). 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":"Validation Specialist","City":"Parsippany","ExpirationDate":null,"PriorityOrder":0,"Requirements":"3+ years validation specialist or engineer within pharma or biopharma Involved in the execution and writing of test protocols Qualification (IQ), Operational Qualification (OQ), Performance Qualification (PQ)Experience with PPQ Batch (Process performance qualification protocol)","Skills":"Veeva Vault or Trackwise Knowledge of Capa and Deviations","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":115200.0000,"SalaryLow":76800.0000,"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 experienced Sr. Validation Specialist to join one of our large pharmaceutical clients for a full-time position. This position will be 5 days a week onsite, in Parsippany,... NJ. This individual will play a crucial role in ensuring quality and compliance of pharmaceutical equipment. The ideal individual will have experience with the execution of validation protocols for various process equipment and systems. This individual will have to assist in the execution of validation test according to established protocols (IQ, OQ, PQ). 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 24, 2024

Bloomsbury, NJ

|

Sales

|

Perm

|

$170k - $310k (estimate)

{"JobID":353340,"JobType":["Perm"],"EmployerID":null,"Location":{"Latitude":-75.0552636363636,"Longitude":40.6511272727273,"Distance":null},"State":"New Jersey","Zip":"08804","ReferenceID":"NNJ-699825","PostedDate":"\/Date(1713971651000)\/","Description":"Insight Global is seeking an experienced Sales Business Development Director for a pharmaceutical manufacturing company client. This is primarily a remote position but 50% travel to prospective customers is required. In this position, you will be tasked expanding the company\u0027s customer base within the Health and Hospitals space. A successful candidate has ability to foster relationships with key stakeholders, expand the existing portfolio by adding new customers , evaluate and identify new prospects to grow market share, increase revenue from existing accounts, and act as a catalyst for future growth. In this role, you will be responsible for a This instrumental position will be reporting directly into the CCO so high level business acumen is expected. 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":"Sales Business Development Director - Health \u0026 Hospital Systems","City":"Bloomsbury","ExpirationDate":null,"PriorityOrder":0,"Requirements":"8+ years of sales experience in a hospital OR, Post Op, ICU, L\u0026D, ER, and health systems facing roleKnowledge of sterile pharmaceutical, medical device, or combination device products Proficiency utilizing CRM systems (Salesforce preferred)Bachelors Degree","Skills":"Experience with 503B regulationsExperience working with customer in the GPO or Health Trust spaceHospital pharmacy Sales experience Masters Degree Experience working for a generic drug manufacturer or healthcare distribution company (i.e. Cardinal health)","Industry":"Sales","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":310000.0000,"SalaryLow":170000.0000,"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 experienced Sales Business Development Director for a pharmaceutical manufacturing company client. This is primarily a remote position but 50% travel to prospective... customers is required. In this position, you will be tasked expanding the company's customer base within the Health and Hospitals space. A successful candidate has ability to foster relationships with key stakeholders, expand the existing portfolio by adding new customers , evaluate and identify new prospects to grow market share, increase revenue from existing accounts, and act as a catalyst for future growth. In this role, you will be responsible for a This instrumental position will be reporting directly into the CCO so high level business acumen is expected. 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 02, 2024

Bridgewater, NJ

|

Managerial / Professional

|

Contract

|

$72 - $108 (hourly estimate)

{"JobID":355133,"JobType":["Contract"],"EmployerID":null,"Location":{"Latitude":-74.6182818181818,"Longitude":40.6080454545455,"Distance":null},"State":"New Jersey","Zip":"08807","ReferenceID":"NNJ-702014","PostedDate":"\/Date(1714677240000)\/","Description":"Insight Global is looking for a Director of Marketing to join the HCP Marketing group for one of our pharmaceutical clients based out of Bridgewater, NJ. This person will be responsible for the development and execution of marketing strategies related to the branded launch of a rare disease drug. It is expected that this person will be able to collaborate with cross-functional partners and lead HCP brand initiatives. This position will report to the Senior Director, HCP Marketing and does not have any direct reports. Currently, this will be a 2 month contract, however, there is potential for extension.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":"Marketing Director","City":"Bridgewater","ExpirationDate":null,"PriorityOrder":0,"Requirements":"Bachelor\u0027s degree required; MBA preferred8+ years of marketing experience in the pharmaceutical industryExperience developing and implementing commercial marketing strategiesExperience with product launchesExperience in managing external partners (e.g. consultants, agencies, healthcare professionals)Highly proficient in Microsoft Office (Word, Excel, PowerPoint, Outlook)","Skills":"Sales experienceExperience in HCP MarketingExperience working with rare disease drug","Industry":"Managerial / Professional","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":108.0000,"SalaryLow":72.0000,"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 Director of Marketing to join the HCP Marketing group for one of our pharmaceutical clients based out of Bridgewater, NJ. This person will be responsible for the... development and execution of marketing strategies related to the branded launch of a rare disease drug. It is expected that this person will be able to collaborate with cross-functional partners and lead HCP brand initiatives. This position will report to the Senior Director, HCP Marketing and does not have any direct reports. Currently, this will be a 2 month contract, however, there is potential for extension.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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