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Jun 18, 2026

Redwood City, CA

|

Project Manager

|

Contract,Perm Possible

|

$64 - $80 (hourly estimate)

{"JobID":543243,"JobType":["Contract,Perm Possible"],"EmployerID":null,"Location":{"Latitude":-122.21,"Longitude":37.49,"Distance":null},"State":"California","Zip":"94063","ReferenceID":"LAX-8ad2a62b-1437-4ebd-8074-a54e96b189ff","PostedDate":"\/Date(1781810343000)\/","Description":"We are seeking an experienced MEP Project Manager to lead the planning, coordination, execution, and delivery of all Mechanical, Electrical, Plumbing, Fire Protection, and Building Controls scopes for a large-scale life sciences project.The MEP Project Manager will serve as the primary leader responsible for managing MEP budgets, schedules, procurement activities, subcontractor performance, design coordination, risk management, commissioning, and project turnover. This role requires close collaboration with project leadership, owners, design consultants, trade partners, commissioning teams, and project controls staff to ensure successful project execution.The ideal candidate will possess 7?15 years of experience managing complex building systems on highly technical projects, preferably within life sciences, pharmaceutical manufacturing, biotechnology, semiconductor, healthcare, mission-critical, or advanced manufacturing environments.Key ResponsibilitiesMEP Project LeadershipLead all MEP project activities from preconstruction through commissioning and final turnover in an office-based capacityServe as the primary management point of contact for mechanical, electrical, plumbing, fire protection, and controls scopesDevelop and maintain strong relationships with owners, architects, engineers, consultants, vendors, and trade partnersCoordinate project objectives with project teams, superintendents, commissioning teams, and project leadershipDrive accountability across all stakeholders to ensure successful project deliveryBudget \u0026 Cost ManagementManage MEP project budgets, forecasts, cost reports, and financial performanceReview and negotiate subcontractor proposals, change orders, and vendor contractsIdentify cost-saving opportunities and participate in value engineering effortsMonitor procurement expenditures and equipment budgets throughout the project lifecycleEvaluate cost impacts associated with design changes, schedule modifications, and project conditionsSchedule ManagementPartner with project leadership and project controls teams to develop and maintain detailed MEP execution plansEnsure procurement, coordination, startup, commissioning, and turnover activities are aligned with project milestonesMonitor critical path activities and identify schedule risksDevelop mitigation and recovery plans to address schedule challengesCoordinate long-lead equipment procurement and delivery schedulesDesign \u0026 Technical CoordinationLead MEP design reviews and constructability assessmentsReview drawings, specifications, RFIs, submittals, shop drawings, and coordination modelsFacilitate resolution of design conflicts and constructability considerationsEnsure MEP systems are coordinated with architectural, structural, process, and operational requirementsSupport BIM/VDC coordination efforts and clash resolution processesProcurement \u0026 Vendor ManagementManage procurement activities for major mechanical and electrical equipment packagesCoordinate equipment manufacturers, suppliers, and specialty vendorsTrack equipment fabrication, shipping, delivery, and startup coordinationMonitor procurement risks and implement contingency plans as necessaryEnsure all materials and equipment meet project specifications and quality requirementsLife Sciences Systems CoordinationOversee coordination and delivery planning for systems commonly found within life sciences and biotechnology environments, including:HVAC and cleanroom systemsProcess and high-purity pipingBuilding automation systems (BAS)Electrical distribution infrastructureEmergency and backup power systemsLaboratory utilitiesEnvironmental control systemsFire alarm and fire protection systemsCentral utility plant equipmentControls and monitoring systemsRisk Management \u0026 Problem SolvingIdentify project risks associated with design, procurement, schedule, labor, quality, and commissioningDevelop mitigation strategies and corrective action plansLead issue resolution efforts among project stakeholdersEscalate critical project concerns and provide recommendations for resolutionMaintain accurate documentation of project decisions and change management activitiesCommissioning \u0026 TurnoverLead MEP turnover strategy from coordination through commissioning and owner acceptanceCoordinate startup, testing, balancing, validation, and commissioning activitiesManage turnover documentation, closeout tracking, and systems acceptanceEnsure operational readiness of all MEP systems prior to owner handoverSupport training activities for facility operations and maintenance personnelQuality \u0026 ComplianceEnsure compliance with applicable building codes, project standards, and owner requirementsParticipate in quality reviews, documentation audits, and corrective action planningSupport project teams in resolving coordination and system integration issuesWe 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":"MEP Senior Project Manager, MD","City":"Redwood City","ExpirationDate":null,"PriorityOrder":0,"Requirements":"7?15 years of project management experience with significant MEP coordination and oversight responsibilitiesExperience managing complex mechanical, electrical, plumbing, fire protection, and controls scopesExperience supporting large-scale projects in one or more of the following sectors:Life SciencesPharmaceutical ManufacturingBiotechnologySemiconductorHealthcareMission Critical / Data CentersAdvanced ManufacturingStrong understanding of project budgeting, forecasting, scheduling, procurement, and contract administrationExperience managing subcontractors, vendors, engineers, and consultants through coordination and performance trackingProficiency in Microsoft Office Suite and project management softwareStrong working knowledge of Primavera P6 schedules and critical path managementExcellent communication, leadership, negotiation, and stakeholder management skillsExperience supporting projects valued at $100M+","Skills":"Direct life sciences, pharmaceutical, or biotech facility experience.Experience with GMP-regulated environments, cleanrooms, and validated systems.Bachelor\u0027s degree in Construction Management, Engineering, Mechanical Engineering, Electrical Engineering, or related field.OSHA 30 certification.","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":80.0000,"SalaryLow":64.0000,"PayRateOvertime":0,"PayRateStraight":0,"Filled":0,"RemainingOpenings":0,"TotalOpenings":0,"Visa":null,"ClearanceType":null,"IsClearanceRequired":false,"IsHealthcare":false,"IsRemote":false,"EndClient":null,"JobCreatedDate":"\/Date(-62135578800000)\/","JobModifiedDate":"\/Date(-62135578800000)\/"}

We are seeking an experienced MEP Project Manager to lead the planning, coordination, execution, and delivery of all Mechanical, Electrical, Plumbing, Fire Protection, and Building Controls scopes... for a large-scale life sciences project.The MEP Project Manager will serve as the primary leader responsible for managing MEP budgets, schedules, procurement activities, subcontractor performance, design coordination, risk management, commissioning, and project turnover. This role requires close collaboration with project leadership, owners, design consultants, trade partners, commissioning teams, and project controls staff to ensure successful project execution.The ideal candidate will possess 7?15 years of experience managing complex building systems on highly technical projects, preferably within life sciences, pharmaceutical manufacturing, biotechnology, semiconductor, healthcare, mission-critical, or advanced manufacturing environments.Key ResponsibilitiesMEP Project LeadershipLead all MEP project activities from preconstruction through commissioning and final turnover in an office-based capacityServe as the primary management point of contact for mechanical, electrical, plumbing, fire protection, and controls scopesDevelop and maintain strong relationships with owners, architects, engineers, consultants, vendors, and trade partnersCoordinate project objectives with project teams, superintendents, commissioning teams, and project leadershipDrive accountability across all stakeholders to ensure successful project deliveryBudget & Cost ManagementManage MEP project budgets, forecasts, cost reports, and financial performanceReview and negotiate subcontractor proposals, change orders, and vendor contractsIdentify cost-saving opportunities and participate in value engineering effortsMonitor procurement expenditures and equipment budgets throughout the project lifecycleEvaluate cost impacts associated with design changes, schedule modifications, and project conditionsSchedule ManagementPartner with project leadership and project controls teams to develop and maintain detailed MEP execution plansEnsure procurement, coordination, startup, commissioning, and turnover activities are aligned with project milestonesMonitor critical path activities and identify schedule risksDevelop mitigation and recovery plans to address schedule challengesCoordinate long-lead equipment procurement and delivery schedulesDesign & Technical CoordinationLead MEP design reviews and constructability assessmentsReview drawings, specifications, RFIs, submittals, shop drawings, and coordination modelsFacilitate resolution of design conflicts and constructability considerationsEnsure MEP systems are coordinated with architectural, structural, process, and operational requirementsSupport BIM/VDC coordination efforts and clash resolution processesProcurement & Vendor ManagementManage procurement activities for major mechanical and electrical equipment packagesCoordinate equipment manufacturers, suppliers, and specialty vendorsTrack equipment fabrication, shipping, delivery, and startup coordinationMonitor procurement risks and implement contingency plans as necessaryEnsure all materials and equipment meet project specifications and quality requirementsLife Sciences Systems CoordinationOversee coordination and delivery planning for systems commonly found within life sciences and biotechnology environments, including:HVAC and cleanroom systemsProcess and high-purity pipingBuilding automation systems (BAS)Electrical distribution infrastructureEmergency and backup power systemsLaboratory utilitiesEnvironmental control systemsFire alarm and fire protection systemsCentral utility plant equipmentControls and monitoring systemsRisk Management & Problem SolvingIdentify project risks associated with design, procurement, schedule, labor, quality, and commissioningDevelop mitigation strategies and corrective action plansLead issue resolution efforts among project stakeholdersEscalate critical project concerns and provide recommendations for resolutionMaintain accurate documentation of project decisions and change management activitiesCommissioning & TurnoverLead MEP turnover strategy from coordination through commissioning and owner acceptanceCoordinate startup, testing, balancing, validation, and commissioning activitiesManage turnover documentation, closeout tracking, and systems acceptanceEnsure operational readiness of all MEP systems prior to owner handoverSupport training activities for facility operations and maintenance personnelQuality & ComplianceEnsure compliance with applicable building codes, project standards, and owner requirementsParticipate in quality reviews, documentation audits, and corrective action planningSupport project teams in resolving coordination and system integration issuesWe 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)

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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/.

Jul 30, 2026

Indianapolis, IN

|

Biomedical Engineering

|

Contract-to-perm

|

$41 - $51 (hourly estimate)

{"JobID":558440,"JobType":["Contract-to-perm"],"EmployerID":null,"Location":{"Latitude":-86.14,"Longitude":39.77,"Distance":null},"State":"Indiana","Zip":"46250","ReferenceID":"IND-a759be20-c5e0-4287-943f-d38282282b36","PostedDate":"\/Date(1785426662000)\/","Description":"Insight Global is looking for a Validation Engineer to support a large HVAC building automation customer. This engineer will go through a series of CQV (Commission, Qualification, Validation) or IQ OQ PQs protocols within an FDA regulated environment for their pharmaceutical customer. Pharma experience is not required but working in a regulated environment is. Ideally this person will have experience managing an environment with human safeties involved. It could be a computer system validation process or a validation equipment process, financial validation, 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":"COPY - Validation Engineer","City":"Indianapolis","ExpirationDate":null,"PriorityOrder":0,"Requirements":"-Bachelor?s degree in an engineering field? ideally Mechanical or Biomedical. -FDA environment experience -Experience reviewing/editing engineering drawings -Local and available to go onsite in Castleton area M-F -Commissioning, validation, qualification (IQ OQ PQ protocols) experience of some kind","Skills":"","Industry":"Biomedical 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":51.0000,"SalaryLow":40.8000,"PayRateOvertime":0,"PayRateStraight":0,"Filled":0,"RemainingOpenings":0,"TotalOpenings":0,"Visa":null,"ClearanceType":null,"IsClearanceRequired":false,"IsHealthcare":false,"IsRemote":false,"EndClient":null,"JobCreatedDate":"\/Date(-62135578800000)\/","JobModifiedDate":"\/Date(-62135578800000)\/"}

Insight Global is looking for a Validation Engineer to support a large HVAC building automation customer. This engineer will go through a series of CQV (Commission, Qualification, Validation) or IQ... OQ PQs protocols within an FDA regulated environment for their pharmaceutical customer. Pharma experience is not required but working in a regulated environment is. Ideally this person will have experience managing an environment with human safeties involved. It could be a computer system validation process or a validation equipment process, financial validation, 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/.

Jul 08, 2026

Holly Springs, NC

|

Project Manager

|

Contract

|

$68 - $85 (hourly estimate)

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Day to Day: A large pharmaceutical client is looking for 2 Sr. Operational Readiness Project Managers to join their team in Raleigh-Durham. In this role you will be responsible for overseeing a... successful turn over of both upstream and downstream equipment to ensure manufacturing is ready for operations. This role will be based onsite 5x per week. ?Lead project scope definition for Operational Readiness workstreams such as Manufacturing, Engineering, Process Development, Supply Chain, and Quality Control, among others?Develop execution strategies, detailed schedules, and risk registers?Integrate and actively facilitate workstreams day-to-day execution?Facilitate teams meetings and execution forums?Represent workstreams in appropriate governance forums?Liaise with other project PMs to ensure effective project delivery?Closely manage schedule performance and provide updates to management?Ensure internal alignment of operational readiness schedules, as well as externally with construction and commissioning/qualification workstreams?Provide strategic guidance on overall project delivery to de-risk and optimize execution?Resolve workstream issues arising throughout the project, manage risk register, and escalate when appropriate to keep objectives and deliverables on track?Lead and facilitate cross-functional workshops required to ensure project alignment, solve project challenges, identify gaps, and advance site strategy?Won't manage people, nor budgetWe are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com.To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/.

Jun 19, 2026

Florham Park, NJ

|

Accounting

|

Perm

|

$136k - $170k (estimate)

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We are seeking a Senior Accounting Manager to lead U.S. accounting operations for a growing pharmaceutical organization. This is a high-impact leadership role responsible for financial reporting,... month-end close, team management, and ensuring strong internal controls across the business.This role partners closely with FP&A, Supply Chain, and cross-functional stakeholders to deliver accurate, timely, and actionable financial insights.What You?ll DoLead the month-end close for U.S. entities, ensuring accurate and timely reporting (IFRS)Oversee journal entries, account reconciliations, and GL activity within SAPPerform variance analysis and investigate key financial movementsManage and develop the accounting team (AP, AR, inventory, accruals, reconciliations)Own the close calendar and ensure all deliverables are metServe as the primary liaison for external audits and manage audit readinessMaintain strong internal controls and ensure compliance (GAAP, IFRS, IRS)Oversee intercompany accounting (royalties, R&D allocations, shared services)Partner cross-functionally with Supply Chain, Commercial, and Regulatory teamsSupport cash management and treasury activitiesDrive process improvements and reporting enhancementsWe are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com.To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/.

Oct 24, 2025

Branford, CT

|

Mechanical Engineering

|

Perm

|

$50k - $62k (estimate)

{"JobID":459696,"JobType":["Perm"],"EmployerID":null,"Location":{"Latitude":-72.7967,"Longitude":41.2778,"Distance":null},"State":"Connecticut","Zip":"06405","ReferenceID":"HTD-d86f5318-c824-4118-b8ab-1b984562538d","PostedDate":"\/Date(1761331644000)\/","Description":"Insight Global is seeking a CNC Machinist to join a Pharmaceutical machine manufacturing company located in Branford, CT. This role will play a critical job in supporting the machine shop and production of complex, custom machines builds. The ideal candidates will produce precision quality parts machining a variety of materials to engineering specification (SS304, 316L, aluminum and a variety of plastics, etc.). Proficiency in setting up, operating, and maintaining ProtoTrak lathes and milling machines to produce precision parts according to technical ISO and ANSI drawings and quality standards. Your day-to-day responsibilities will include:-Ability to set up, troubleshoot, and operate CNC 3-Axis Machines.-Inspect work completed on CNC 3-Axis Machines for conformance to specifications using bench gauging.-Strictly follow Standard Work in all aspects of work including CNC Machine setup and operation, process verification, product inspection, documentation, and material handling.-Perform light preventative maintenance tasks on CNC Machines to maintain machinery performance and prevent machine downtime.-Comply with all company and safety rules and regulations.-Complete testing and adjustment of parts, as needed.We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com.To learn more about how we collect, keep, and process your private information, please review Insight Global\u0027s Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/.","Title":"CNC Machinist","City":"Branford","ExpirationDate":null,"PriorityOrder":0,"Requirements":"-CNC 3 \u0026 5 Axis Machining Experience (min. 3-5 years of experience)-Ability to read an interpret blueprints and technical drawings - Familiar with the metric system-1st shift: 7am-3:30p as these roles will transition to nights after training (training on day shift) -Ability to perform their own set ups and operate - NOT seeking Machine OPERATORS - Fully skilled MACHINIST.","Skills":"-Programming and operating ProtoTrak controls.-ISO \u0026 ANSI drawing print reading a plus!-Experience in turning lathe is a plus","Industry":"Mechanical Engineering","Country":"US","Division":"AF\u0026E","Office":null,"IsRemoteJob":false,"IsInternalJob":false,"ExtraValues":null,"__RecordIndex":0,"__OrdinalPosition":0,"__Timestamp":0,"Status":null,"ApplicantCount":0,"SubmittalCount":0,"ApplicationToHireRatio":0,"JobDuration":null,"SalaryHigh":62400.0000,"SalaryLow":49920.0000,"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 CNC Machinist to join a Pharmaceutical machine manufacturing company located in Branford, CT. This role will play a critical job in supporting the machine shop and... production of complex, custom machines builds. The ideal candidates will produce precision quality parts machining a variety of materials to engineering specification (SS304, 316L, aluminum and a variety of plastics, etc.). Proficiency in setting up, operating, and maintaining ProtoTrak lathes and milling machines to produce precision parts according to technical ISO and ANSI drawings and quality standards. Your day-to-day responsibilities will include:-Ability to set up, troubleshoot, and operate CNC 3-Axis Machines.-Inspect work completed on CNC 3-Axis Machines for conformance to specifications using bench gauging.-Strictly follow Standard Work in all aspects of work including CNC Machine setup and operation, process verification, product inspection, documentation, and material handling.-Perform light preventative maintenance tasks on CNC Machines to maintain machinery performance and prevent machine downtime.-Comply with all company and safety rules and regulations.-Complete testing and adjustment of parts, as needed.We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com.To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/.

Aug 06, 2026

Bothell, WA

|

Materials Science & Engineering

|

Contract

|

$29 - $36 (hourly estimate)

{"JobID":561434,"JobType":["Contract"],"EmployerID":null,"Location":{"Latitude":-122.2,"Longitude":47.79,"Distance":null},"State":"Washington","Zip":"98021","ReferenceID":"PHL-ff5d406b-7022-4fab-b434-3a0866ae6960","PostedDate":"\/Date(1786046650000)\/","Description":"A leading pharmaceutical organization is seeking a Sr. Associate Scientist to support antibody and recombinant protein generation efforts within its Protein Sciences team. This individual will be responsible for hands-on laboratory activities spanning DNA design, molecular cloning, protein expression, purification, and characterization. The ideal candidate will have strong laboratory experience in recombinant protein production and be comfortable working independently in a fast-paced research environment.Responsibilities:- Design DNA sequences and support vector construction activities.- Perform molecular biology techniques including cloning, sequencing verification, plasmid preparation, and quality control.- Produce recombinant proteins, including antibodies, biospecifics, fusion proteins, and other protein modalities using mammalian expression systems.- Purify proteins using affinity chromatography and other purification techniques.- Conduct analytical characterization of purified proteins to assess quality, concentration, and functionality.- Fulfill laboratory reagent and protein production requests while maintaining accurate documentation.- Collaborate with cross-functional scientists to support ongoing research programs.- Maintain laboratory equipment, inventory, and compliance with established safety protocols.- Analyze experimental results and communicate findings to project teams.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 Associate Scientist - Protein Solutions","City":"Bothell","ExpirationDate":null,"PriorityOrder":0,"Requirements":"- Bachelor?s degree in biochemistry, chemistry, or related field with a minimum of 2 years relevant experience, or equivalent degree.- Hands-on laboratory experience (excluding collegework)- Experience with recombinant protein production from DNA design to quality analysis- Prior experience working with electronic lab notebooks and/or LIMS systems","Skills":"- Experience with python scripting and/or strong excel macro skills- Experience with annotating antibody sequences and familiarity with antibody structure/domains- Experience with product quality analysis for antibodies and recombinant proteins- Antibody-drug conjugate and small compound handling experience","Industry":"Materials Science \u0026 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":36.0000,"SalaryLow":28.8000,"PayRateOvertime":0,"PayRateStraight":0,"Filled":0,"RemainingOpenings":0,"TotalOpenings":0,"Visa":null,"ClearanceType":null,"IsClearanceRequired":false,"IsHealthcare":false,"IsRemote":false,"EndClient":null,"JobCreatedDate":"\/Date(-62135578800000)\/","JobModifiedDate":"\/Date(-62135578800000)\/"}

A leading pharmaceutical organization is seeking a Sr. Associate Scientist to support antibody and recombinant protein generation efforts within its Protein Sciences team. This individual will be... responsible for hands-on laboratory activities spanning DNA design, molecular cloning, protein expression, purification, and characterization. The ideal candidate will have strong laboratory experience in recombinant protein production and be comfortable working independently in a fast-paced research environment.Responsibilities:- Design DNA sequences and support vector construction activities.- Perform molecular biology techniques including cloning, sequencing verification, plasmid preparation, and quality control.- Produce recombinant proteins, including antibodies, biospecifics, fusion proteins, and other protein modalities using mammalian expression systems.- Purify proteins using affinity chromatography and other purification techniques.- Conduct analytical characterization of purified proteins to assess quality, concentration, and functionality.- Fulfill laboratory reagent and protein production requests while maintaining accurate documentation.- Collaborate with cross-functional scientists to support ongoing research programs.- Maintain laboratory equipment, inventory, and compliance with established safety protocols.- Analyze experimental results and communicate findings to project teams.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/.

Jul 06, 2026

New Haven, CT

|

Nurse

|

Contract

|

$42 - $53 (hourly estimate)

{"JobID":548278,"JobType":["Contract"],"EmployerID":null,"Location":{"Latitude":-72.9383,"Longitude":41.3255,"Distance":null},"State":"Connecticut","Zip":"06511","ReferenceID":"HNJ-b9f7d066-1849-4506-be28-40ca093fde1f","PostedDate":"\/Date(1783320540000)\/","Description":"Insight Global is looking for clinical trial support staff to join our vaccine development team at a large pharmaceutical company in New Haven, CT. As a clinical trial support staff member, you will be responsible for coordinating and conducting clinical trials for new vaccine candidates, ensuring compliance with protocols, regulations, and ethical standards. You will also monitor and report on the safety and efficacy of the vaccine candidates, provide education and support to trial participants, and collaborate with other health professionals and researchers. To be successful in this role, you will need any of the following: an RN license, an LPN license, or a paramedic license, and at least 3-5 years of experience in a clinical setting. You will also need excellent communication, organizational, and problem-solving skills, as well as a passion for advancing public health through innovation.The working hours are 11-7 with some flexibility with the ability to work 4 weekend shifts a month along with holidays. This individual will be brought on to support vaccine development in human patients but will eventually move on to different projects once the vaccine development is completed.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":"Clinical RN (1st and 2nd Shift)","City":"New Haven","ExpirationDate":null,"PriorityOrder":0,"Requirements":"5 years of experience as an RN 2 years of clinical trials or clinical research experience RN license in Connecticut Experience taking vitals, overseeing meals as data, blood draws, EKG/ECG, working with clinical coordinators/project managers, working with pharmacy/lab/front deskExperience with Discharge planning","Skills":"","Industry":"Nurse","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":53.0000,"SalaryLow":42.4000,"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 clinical trial support staff to join our vaccine development team at a large pharmaceutical company in New Haven, CT. As a clinical trial support staff member, you will... be responsible for coordinating and conducting clinical trials for new vaccine candidates, ensuring compliance with protocols, regulations, and ethical standards. You will also monitor and report on the safety and efficacy of the vaccine candidates, provide education and support to trial participants, and collaborate with other health professionals and researchers. To be successful in this role, you will need any of the following: an RN license, an LPN license, or a paramedic license, and at least 3-5 years of experience in a clinical setting. You will also need excellent communication, organizational, and problem-solving skills, as well as a passion for advancing public health through innovation.The working hours are 11-7 with some flexibility with the ability to work 4 weekend shifts a month along with holidays. This individual will be brought on to support vaccine development in human patients but will eventually move on to different projects once the vaccine development is completed.We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com.To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/.

Jun 10, 2026

Malvern, PA

|

Engineering (Non IT)

|

Contract

|

$28 - $35 (hourly estimate)

{"JobID":539891,"JobType":["Contract"],"EmployerID":null,"Location":{"Latitude":-75.51,"Longitude":40.03,"Distance":null},"State":"Pennsylvania","Zip":"19355","ReferenceID":"PHL-0cc433ef-cd35-4011-bd3c-f434436aa4b4","PostedDate":"\/Date(1781100848000)\/","Description":"One of our large pharmaceutical clients is looking to hire an Associate Scientist of Cell Banking to perform Cell Banking for the Cell Culture processes and/or bio-analytical testing within the API Large Molecule Process Development group in Malvern PA. The candidate\u0027s primary responsibilities will include but are not limited to the production, testing, inventory, and supply of Master, Working, and development Cell Banks for clinical, and commercial production as well as analytical testing for biopharmaceutical and cell therapy products. Responsibilities will include: -Support Cell banking organization by performing Cell banking for Cell Culture processes and analytical testing. -Execute production, testing, and release of Master, Working, development, and analytical cell Banks and ensures the timely supply to customers. -Work in a team environment as well as contributing individually to meet project timeline and objectives. -Participate in Cell culture and cryopreservation of cells using aseptic techniques under GMP Compliant conditions. -Execute all activities per established procedures and protocols -Interface with internal and external customers to ship cell banks and supply critical information as per their requirements. -Collaborate cross-functionally to represent Cell Banking department. -Author, review, and approve technical documents, SOPs, and batch records.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":"Associate Scientist, Cell Banking","City":"Malvern","ExpirationDate":null,"PriorityOrder":0,"Requirements":"-Bachelor\u0027s degree in scientific field, preferably Biotech -Minimum 1 year of experience working in a lab environment, preferably GMP -Minimum 1-2 years of experience working within cell culture -Minimum 1 year of experience working with Aseptic techniques -GDP (Good documentation practice) -Strong attention to detail -Extremely motivated individual","Skills":"-Cell Banking experience -Experience maintaining writing records of work in form of (electronic) notebooks, procedural documents, protocols and technical reports is preferred. -Experience working with electronic laboratory tracking system, inventory management systems -Automatic cell counting experience, Vi-CELL","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":35.0000,"SalaryLow":28.0000,"PayRateOvertime":0,"PayRateStraight":0,"Filled":0,"RemainingOpenings":0,"TotalOpenings":0,"Visa":null,"ClearanceType":null,"IsClearanceRequired":false,"IsHealthcare":false,"IsRemote":false,"EndClient":null,"JobCreatedDate":"\/Date(-62135578800000)\/","JobModifiedDate":"\/Date(-62135578800000)\/"}

One of our large pharmaceutical clients is looking to hire an Associate Scientist of Cell Banking to perform Cell Banking for the Cell Culture processes and/or bio-analytical testing within the API... Large Molecule Process Development group in Malvern PA. The candidate's primary responsibilities will include but are not limited to the production, testing, inventory, and supply of Master, Working, and development Cell Banks for clinical, and commercial production as well as analytical testing for biopharmaceutical and cell therapy products. Responsibilities will include: -Support Cell banking organization by performing Cell banking for Cell Culture processes and analytical testing. -Execute production, testing, and release of Master, Working, development, and analytical cell Banks and ensures the timely supply to customers. -Work in a team environment as well as contributing individually to meet project timeline and objectives. -Participate in Cell culture and cryopreservation of cells using aseptic techniques under GMP Compliant conditions. -Execute all activities per established procedures and protocols -Interface with internal and external customers to ship cell banks and supply critical information as per their requirements. -Collaborate cross-functionally to represent Cell Banking department. -Author, review, and approve technical documents, SOPs, and batch records.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 22, 2026

Brunswick, GA

|

Business Analyst (BA)

|

Contract

|

$34 - $42 (hourly estimate)

{"JobID":533425,"JobType":["Contract"],"EmployerID":null,"Location":{"Latitude":-81.48,"Longitude":31.15,"Distance":null},"State":"Georgia","Zip":"31520","ReferenceID":"HJX-76ee58d4-416d-4725-927b-6245ac9b6936","PostedDate":"\/Date(1779463637000)\/","Description":"A midsize community health system in Southeast, GA is seeking a junior business analyst to join their team. This person will be playing a critical role in meeting directly with operational and IT stakeholders to bridge the gap on requirements specifically related to BI and data analytics. They will be part of a team of 9 and report directly to the Director of Data Analytics. They should be skilled in interviewing stakeholders for requirements gathering, able to wireframe, proven ability to author technical user stories for their developers, and strong stakeholder management experience working with high level operational leaders. The ideal candidate will have experience in healthcare or a healthcare adjacent industry such as pharmaceutical or medical devices. This role is on-site 5 days a week in Brunswick, GA. This will be a 3 month contract with opportunity for extensions.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","City":"Brunswick","ExpirationDate":null,"PriorityOrder":0,"Requirements":"? 4-6 years of experience as a business analyst for mid-large enterprise company? Experience gathering requirements directly from operational and IT leaders? Ability to author user stories \u0026 wireframe? Healthcare background (ability to understand data requests pertaining to a heavily regulated environment)Excellent communication and interpersonal skills","Skills":"? Dashboarding/visualization experience with Power BIAgile certification","Industry":"Business Analyst (BA)","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":42.0000,"SalaryLow":33.6000,"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 midsize community health system in Southeast, GA is seeking a junior business analyst to join their team. This person will be playing a critical role in meeting directly with operational and IT... stakeholders to bridge the gap on requirements specifically related to BI and data analytics. They will be part of a team of 9 and report directly to the Director of Data Analytics. They should be skilled in interviewing stakeholders for requirements gathering, able to wireframe, proven ability to author technical user stories for their developers, and strong stakeholder management experience working with high level operational leaders. The ideal candidate will have experience in healthcare or a healthcare adjacent industry such as pharmaceutical or medical devices. This role is on-site 5 days a week in Brunswick, GA. This will be a 3 month contract with opportunity for extensions.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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