job summary: Regulatory Affairs Manager II 12 Month Contract | REMOTE Join a leading biopharma company supporting critical regulatory systems initiatives. We're seeking a detail-oriented consultant with expertise in Regulatory Systems, eCTD submission management, and experience working with global IT and cross-functional teams to drive system implementation and Quality Control Process, Documentation & Testing. Key Focus Areas: Regulatory Systems Expertise
job summary: Regulatory Affairs Manager II 12 Month Contract | REMOTE Join a leading biopharma company supporting critical regulatory systems initiatives. We're seeking a detail-oriented consultant with expertise in Regulatory Systems, eCTD submission management, and experience working with global IT and cross-functional teams to drive system implementation and Quality Control Process, Documentation & Testing. Key Focus Areas: Regulatory Systems Expertise
job summary: REGULATORY AFFAIRS MANAGER | 100% Remote (EST Coast based) We're supporting a high-impact Regulatory Submissions Delivery role focused on US and EU regions, with global scope. What we're looking for: 3-5 years of Submission Delivery Support experienceStrong knowledge of US & EU regulatory requirementsBackground in publishing and vendor management a big plusExperience with NDA/MAA filings and larger submissionsSkilled in lifecycle submission
job summary: REGULATORY AFFAIRS MANAGER | 100% Remote (EST Coast based) We're supporting a high-impact Regulatory Submissions Delivery role focused on US and EU regions, with global scope. What we're looking for: 3-5 years of Submission Delivery Support experienceStrong knowledge of US & EU regulatory requirementsBackground in publishing and vendor management a big plusExperience with NDA/MAA filings and larger submissionsSkilled in lifecycle submission
job summary: As the largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. A current top partnership with a research-driven biopharmaceutical company is known as a powerhouse that
job summary: As the largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. A current top partnership with a research-driven biopharmaceutical company is known as a powerhouse that
job summary: Responsible for collection and testing of routine environmental monitoring samples within aseptic processing fill lines, Isolator fill line, compounding, sterility suite, and component preparation areas for aseptic lines (Building A) and clean rooms areas in new expansion Building B. Collect and test utility samples such as WFI, clean steam and compressed gases. Monitors environmental conditions in laboratory areas during test sessions. Repor
job summary: Responsible for collection and testing of routine environmental monitoring samples within aseptic processing fill lines, Isolator fill line, compounding, sterility suite, and component preparation areas for aseptic lines (Building A) and clean rooms areas in new expansion Building B. Collect and test utility samples such as WFI, clean steam and compressed gases. Monitors environmental conditions in laboratory areas during test sessions. Repor
job summary: The Medical Editor, Value & Access, is responsible for reviewing, editing, and supporting documents developed by Value & Access including AMCP dossiers, compendia, and product monographs. This individual provides editorial expertise for multiple projects across therapeutic areas within established timelines, interfaces regularly with medical writers to ensure accurate and timely delivery of information and contributes to cross-functional meet
job summary: The Medical Editor, Value & Access, is responsible for reviewing, editing, and supporting documents developed by Value & Access including AMCP dossiers, compendia, and product monographs. This individual provides editorial expertise for multiple projects across therapeutic areas within established timelines, interfaces regularly with medical writers to ensure accurate and timely delivery of information and contributes to cross-functional meet
job summary: A current top partnership with a research-driven biopharmaceutical company is known as a powerhouse that aims to develop treatments for difficult-to-cure diseases. This renowned employer has created 32 products, that have highly impacted lives across the globe. If you're looking to stand out in your field and lead the way to innovative therapies, this position is for you! location: North Chicago, Illinois job type: Contract salary: &#x
job summary: A current top partnership with a research-driven biopharmaceutical company is known as a powerhouse that aims to develop treatments for difficult-to-cure diseases. This renowned employer has created 32 products, that have highly impacted lives across the globe. If you're looking to stand out in your field and lead the way to innovative therapies, this position is for you! location: North Chicago, Illinois job type: Contract salary: &#x
job summary: The Medical Device Safety team is a highly diverse department that plays a critical role in conceptualizing, designing, and implementing high-priority analytical strategies, clinical oversight, and initiatives. The team is a high-profile high-impact team that works with PPS functions on a range of product initiatives. As a member of the team, you are at the forefront of working with leaders to identify critical priorities and drive high-value
job summary: The Medical Device Safety team is a highly diverse department that plays a critical role in conceptualizing, designing, and implementing high-priority analytical strategies, clinical oversight, and initiatives. The team is a high-profile high-impact team that works with PPS functions on a range of product initiatives. As a member of the team, you are at the forefront of working with leaders to identify critical priorities and drive high-value
job summary: Randstad Life Sciences is working with a global leader in the manufacture of cGMP-produced, high purity, injectable grade excipients and bioprocessing solutions. We are looking for someone to join their program and further their career! This candidates needs to possess the following API HPLC ICP-MS EMPOWER ANALAYTICAL METHOD DEVELOPMENT ANALAYTICAL METHOD VALIDATION QC Individual will perform testing of raw materials, in process samples, fini
job summary: Randstad Life Sciences is working with a global leader in the manufacture of cGMP-produced, high purity, injectable grade excipients and bioprocessing solutions. We are looking for someone to join their program and further their career! This candidates needs to possess the following API HPLC ICP-MS EMPOWER ANALAYTICAL METHOD DEVELOPMENT ANALAYTICAL METHOD VALIDATION QC Individual will perform testing of raw materials, in process samples, fini
job summary: As the largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. A current top partnership with a research-driven biopharmaceutical company is known as a powerhouse that
job summary: As the largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. A current top partnership with a research-driven biopharmaceutical company is known as a powerhouse that
The Manufacturing Technician I is responsible for executing processes in production at Takeda’s manufacturing facility in Round Lake, Illinois, while strictly adhering to cGMP, environmental health and safety guidelines and any other related regulations that apply. The incumbent will fully participate in both departmental projects and any quality working teams which may be applicable. Responsibilities include hands-on execution of all activities in t
The Manufacturing Technician I is responsible for executing processes in production at Takeda’s manufacturing facility in Round Lake, Illinois, while strictly adhering to cGMP, environmental health and safety guidelines and any other related regulations that apply. The incumbent will fully participate in both departmental projects and any quality working teams which may be applicable. Responsibilities include hands-on execution of all activities in t
The Manufacturing Technician I is responsible for executing processes in production at Takeda’s manufacturing facility in Round Lake, Illinois, while strictly adhering to cGMP, environmental health and safety guidelines and any other related regulations that apply. The incumbent will fully participate in both departmental projects and any quality working teams which may be applicable. Responsibilities include hands-on execution of all activities in t
The Manufacturing Technician I is responsible for executing processes in production at Takeda’s manufacturing facility in Round Lake, Illinois, while strictly adhering to cGMP, environmental health and safety guidelines and any other related regulations that apply. The incumbent will fully participate in both departmental projects and any quality working teams which may be applicable. Responsibilities include hands-on execution of all activities in t
job summary: Ensures accurate and consistent coding of medical data, including but not limited to, adverse event verbatim descriptions and medication data received from global clinical trials across all clinical areas including identification of prohibited medications and exclusionary medical history. Participates in Centralized Clinical Coding Group (CCCG) process improvement initiatives and serves as a subject matter expert and primary coding resource f
job summary: Ensures accurate and consistent coding of medical data, including but not limited to, adverse event verbatim descriptions and medication data received from global clinical trials across all clinical areas including identification of prohibited medications and exclusionary medical history. Participates in Centralized Clinical Coding Group (CCCG) process improvement initiatives and serves as a subject matter expert and primary coding resource f
job summary: Responsible for performing the accurate and detailed medical review of complex advertising and promotional materials and non-promotional materials. Provides timely and accurate reviews of promotional materials in accordance with established policies and practice standards, including regulatory guidelines to meet customer needs. Ensures deliverables convey a clear and appropriate medical message. location: Telecommute job type: Contract s
job summary: Responsible for performing the accurate and detailed medical review of complex advertising and promotional materials and non-promotional materials. Provides timely and accurate reviews of promotional materials in accordance with established policies and practice standards, including regulatory guidelines to meet customer needs. Ensures deliverables convey a clear and appropriate medical message. location: Telecommute job type: Contract s
job summary: The Biologics Drug Product Development team develops antibody drug conjugates (ADC) and other biologics by state-of-the-art formulation and analytical technologies. We create valuable intellectual property through new formulation compositions, cost effective manufacturing processes and prepare and defend CMC (Chemistry, Manufacturing and Control) regulatory content. We are looking for a highly motivated person to support Developability and Fo
job summary: The Biologics Drug Product Development team develops antibody drug conjugates (ADC) and other biologics by state-of-the-art formulation and analytical technologies. We create valuable intellectual property through new formulation compositions, cost effective manufacturing processes and prepare and defend CMC (Chemistry, Manufacturing and Control) regulatory content. We are looking for a highly motivated person to support Developability and Fo
job summary: The Analytical Development-Early Stage group within Biologics ARD is responsible for support of programs that are preparing for FIH clinical studies. The team leads Stage 1 method development, optimization, and validation. In collaboration with cross-functional partners, the team supports early phase formulation and process development studies. Key deliverables include product control strategies informed by analytical data and method understa
job summary: The Analytical Development-Early Stage group within Biologics ARD is responsible for support of programs that are preparing for FIH clinical studies. The team leads Stage 1 method development, optimization, and validation. In collaboration with cross-functional partners, the team supports early phase formulation and process development studies. Key deliverables include product control strategies informed by analytical data and method understa
job summary: We seek a multidisciplinary scientist to join the Company's Discovery Immuno-oncology to perform proof of concept experiments to advance novel therapeutic modalities. The successful candidate will apply skills in cellular and molecular biology, biochemistry, immunology, and/or cancer biology to perform proof of concept studies for novel oncology drugs. This person will leverage these skills as a member of the cross-functional team to support
job summary: We seek a multidisciplinary scientist to join the Company's Discovery Immuno-oncology to perform proof of concept experiments to advance novel therapeutic modalities. The successful candidate will apply skills in cellular and molecular biology, biochemistry, immunology, and/or cancer biology to perform proof of concept studies for novel oncology drugs. This person will leverage these skills as a member of the cross-functional team to support
job summary: Role is responsible for designing, planning, and executing large scale data analysis, and algorithm development to identify gaps in the care continuum and to measure impact using RWD. This work highlights the value of utilizing real world data to inform or address strategic questions in the disease areas of interest. The role involves the application of statistical theories, analytical methods, and technical programming skills to analyze clin
job summary: Role is responsible for designing, planning, and executing large scale data analysis, and algorithm development to identify gaps in the care continuum and to measure impact using RWD. This work highlights the value of utilizing real world data to inform or address strategic questions in the disease areas of interest. The role involves the application of statistical theories, analytical methods, and technical programming skills to analyze clin
job summary: Role is responsible for designing, planning, and executing large scale data analysis, and algorithm development to identify gaps in the care continuum and to measure impact using RWD. This work highlights the value of utilizing real world data to inform or address strategic questions in the disease areas of interest. The role involves the application of statistical theories, analytical methods, and technical programming skills to analyze clin
job summary: Role is responsible for designing, planning, and executing large scale data analysis, and algorithm development to identify gaps in the care continuum and to measure impact using RWD. This work highlights the value of utilizing real world data to inform or address strategic questions in the disease areas of interest. The role involves the application of statistical theories, analytical methods, and technical programming skills to analyze clin
job summary: One of our premier partnerships is with a research-driven biopharmaceutical powerhouse focused on developing treatments for complex, hard-to-cure diseases. This esteemed company has brought 32 groundbreaking products to market, making a significant global impact. If you're ready to make your mark in the field and contribute to the future of innovative therapies, this is the opportunity for you! location: Telecommute job type: Contract sa
job summary: One of our premier partnerships is with a research-driven biopharmaceutical powerhouse focused on developing treatments for complex, hard-to-cure diseases. This esteemed company has brought 32 groundbreaking products to market, making a significant global impact. If you're ready to make your mark in the field and contribute to the future of innovative therapies, this is the opportunity for you! location: Telecommute job type: Contract sa
A Global Biotech/Pharma located in Round Lake, IL is seeking a Manufacturing Technician to join their Team! Support manufacturing operations in Inspection and/or Packaging Inspect manufactured product for irregularities or defects Supplies components, small parts, glassware, tubing, etc. to cell culture and purification areas Operate general production equipment (such as labelers, parts washers, autoclave, stir plates, etc.) Complete relevant paperwork fo
A Global Biotech/Pharma located in Round Lake, IL is seeking a Manufacturing Technician to join their Team! Support manufacturing operations in Inspection and/or Packaging Inspect manufactured product for irregularities or defects Supplies components, small parts, glassware, tubing, etc. to cell culture and purification areas Operate general production equipment (such as labelers, parts washers, autoclave, stir plates, etc.) Complete relevant paperwork fo
job summary: A research-driven biopharmaceutical company is known as a powerhouse that aims to develop treatments for difficult-to-cure diseases. This renowned employer has created 32 products, including Humira and Lupron, that have highly impacted lives across the globe. If you're looking to stand out in your field and lead the way to innovative therapies, this position is for you! location: North Chicago, Illinois job type: Contract salary: $
job summary: A research-driven biopharmaceutical company is known as a powerhouse that aims to develop treatments for difficult-to-cure diseases. This renowned employer has created 32 products, including Humira and Lupron, that have highly impacted lives across the globe. If you're looking to stand out in your field and lead the way to innovative therapies, this position is for you! location: North Chicago, Illinois job type: Contract salary: $
