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8 jobs found in bridgewater, new jersey

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    • new brunswick, new jersey
    • contract
    • $45 - $50 per hour
    job summary: The Contractor, Pharmacology is responsible for planning, performing, and analyzing the results of scientific experiments that contribute to research and drug discovery activities. The incumbent works cross-functionally with internal departments, and external resources as appropriate, as part of discovery science project teams. A primary focus will be identifying and developing new therapies for muscular dystrophy and identifying new indications for existing products.   location: New Brunswick, New Jersey job type: Contract salary: $45 - 50 per hour work hours: 9 to 5 education: Bachelors   responsibilities: With guidance from the plans and executes scientific research and experiments and interprets and communicates results as part of multi-disciplinary team(s).Investigates the feasibility of applying a wide variety of scientific principles and concepts to research problems.Presents findings internally to cross-functional teams.Abides by all safety and regulatory guidelines.Maintains a detailed laboratory notebook.Performs other tasks as assignedAbides by all safety requirements and IACUC guidelinesContributes to general lab needs such as: Equipment maintenance.Capital equipment purchases.Troubleshoot   qualifications: B.S in a scientific discipline preferably Biochemistry, Physiology, Neuroscience or Toxicology with 6 years of experience or an MS degree with 2 years of experience.Hands on experience with small animals such as rodents including dosing, but may not be limited, performing IV/IP/SC/ICV injections in mice and perform anesthesia and monitor animal health.Experience in functional assessment in rodent models of muscular and neuromuscular disease.Hands on experience with measuring functional and behavior assays in rodent models of muscular and neuromuscular disease.Experience with transgenic mouse model. This include, but may not limited to, colony maintenance, breeding, PCR genotyping, behavioral & functional testing. Demonstrate ability to work on complex problems to produce experimental data across one or more projects.Exercises independent judgement within defined procedures and practices.Demonstrates technical proficiency, collaboration with others within a fast-paced, matrixed, team environment consisting of internal and external team members.Possesses detailed and expert knowledge of scientific principles and concepts.Demonstrate ability to work effectively in a multi-disciplinary team environment.Experience and proficiency in working with data/statistical analysis software packages such as GraphPad/Prism. Experience and proficiency in working with data/statistical analysis software packages and languages such as R, RStudio, Python, Pandas helpful.Proficiency with Microsoft Office preferably MS Excel and MS PowerPoint or similarExcellent verbal and written communication and skills.Analytical thinker with excellent problem-solving skills.Demonstrates an understanding of the strategic alignment of his/her work with corporate goal(s) and demonstrates the ability to adapt to changing priorities and deadlines.Excellent planning, organization and time management skills including the ability to support and prioritize multiple projects. Preferred: Experience in designing and conducting studies in models muscular and neuromuscular diseases.Demonstrated knowledge and understanding of rodent and non-rodent models for neurological disease indications, including transgenic and knock-out mice and rats.  skills: Pharmacology Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    job summary: The Contractor, Pharmacology is responsible for planning, performing, and analyzing the results of scientific experiments that contribute to research and drug discovery activities. The incumbent works cross-functionally with internal departments, and external resources as appropriate, as part of discovery science project teams. A primary focus will be identifying and developing new therapies for muscular dystrophy and identifying new indications for existing products.   location: New Brunswick, New Jersey job type: Contract salary: $45 - 50 per hour work hours: 9 to 5 education: Bachelors   responsibilities: With guidance from the plans and executes scientific research and experiments and interprets and communicates results as part of multi-disciplinary team(s).Investigates the feasibility of applying a wide variety of scientific principles and concepts to research problems.Presents findings internally to cross-functional teams.Abides by all safety and regulatory guidelines.Maintains a detailed laboratory notebook.Performs other tasks as assignedAbides by all safety requirements and IACUC guidelinesContributes to general lab needs such as: Equipment maintenance.Capital equipment purchases.Troubleshoot   qualifications: B.S in a scientific discipline preferably Biochemistry, Physiology, Neuroscience or Toxicology with 6 years of experience or an MS degree with 2 years of experience.Hands on experience with small animals such as rodents including dosing, but may not be limited, performing IV/IP/SC/ICV injections in mice and perform anesthesia and monitor animal health.Experience in functional assessment in rodent models of muscular and neuromuscular disease.Hands on experience with measuring functional and behavior assays in rodent models of muscular and neuromuscular disease.Experience with transgenic mouse model. This include, but may not limited to, colony maintenance, breeding, PCR genotyping, behavioral & functional testing. Demonstrate ability to work on complex problems to produce experimental data across one or more projects.Exercises independent judgement within defined procedures and practices.Demonstrates technical proficiency, collaboration with others within a fast-paced, matrixed, team environment consisting of internal and external team members.Possesses detailed and expert knowledge of scientific principles and concepts.Demonstrate ability to work effectively in a multi-disciplinary team environment.Experience and proficiency in working with data/statistical analysis software packages such as GraphPad/Prism. Experience and proficiency in working with data/statistical analysis software packages and languages such as R, RStudio, Python, Pandas helpful.Proficiency with Microsoft Office preferably MS Excel and MS PowerPoint or similarExcellent verbal and written communication and skills.Analytical thinker with excellent problem-solving skills.Demonstrates an understanding of the strategic alignment of his/her work with corporate goal(s) and demonstrates the ability to adapt to changing priorities and deadlines.Excellent planning, organization and time management skills including the ability to support and prioritize multiple projects. Preferred: Experience in designing and conducting studies in models muscular and neuromuscular diseases.Demonstrated knowledge and understanding of rodent and non-rodent models for neurological disease indications, including transgenic and knock-out mice and rats.  skills: Pharmacology Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • parsippany, new jersey
    • contract
    • $18 - $23.94 per hour
    job summary: This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation. As the world's 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. With therapeutic areas that include Oncology, Vaccines, and Rare Diseases, our partner aims to make treatments streamlined, easily accessible, and globally produced. If you share their goal of approaching healthcare in a novel way, look no further - apply for your dream job now!   location: Parsippany, New Jersey job type: Contract salary: $18.00 - 23.94 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Provides analytical support to client groups.Analytical research and development activities will include literature searches, analytical method development, test procedure writing, analytical method validation, and method transfer. Analyzes early stage prototypes, lab samples, pilot plant samples, production samples, stability samples and competitor samples. Possesses extensive knowledge of various laboratory instruments like HPLC, GC, AA, Dissolution, IC, etc.  qualifications: MUST HAVE 1-3 years lab experienceBachelor Degree in Chem or Science is a must MS= okay as well Ideal: Chemistry 2 - 4 Years empower 3 software 2 - 4 Years  skills: HPLC, Chemistry Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    job summary: This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation. As the world's 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. With therapeutic areas that include Oncology, Vaccines, and Rare Diseases, our partner aims to make treatments streamlined, easily accessible, and globally produced. If you share their goal of approaching healthcare in a novel way, look no further - apply for your dream job now!   location: Parsippany, New Jersey job type: Contract salary: $18.00 - 23.94 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Provides analytical support to client groups.Analytical research and development activities will include literature searches, analytical method development, test procedure writing, analytical method validation, and method transfer. Analyzes early stage prototypes, lab samples, pilot plant samples, production samples, stability samples and competitor samples. Possesses extensive knowledge of various laboratory instruments like HPLC, GC, AA, Dissolution, IC, etc.  qualifications: MUST HAVE 1-3 years lab experienceBachelor Degree in Chem or Science is a must MS= okay as well Ideal: Chemistry 2 - 4 Years empower 3 software 2 - 4 Years  skills: HPLC, Chemistry Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • whippany, new jersey (remote)
    • contract
    • $42.85 - $50.41 per hour
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to find 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. We supply prestigious life sciences and biopharma companies with job seekers like you to achieve their business goals. If you're looking for a position where you can serve as an asset to your company while making a difference in others' lives, we have the ideal position for you!   location: Whippany, New Jersey job type: Contract salary: $42.85 - 50.41 per hour work hours: 8 to 4 education: Bachelors   responsibilities: This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation. DEPARTMENT/TEAM DESCRIPTION Operational Excellence and Project Management in Global Medical Affairs (GMA), Oncology SBU is a global function which partners and collaborates with the MA Teams and Key Stakeholders (internal and external) to assist in achieving short and long term strategic goals while adhering to "LIFE" values (leadership, integrity, flexibility, efficiency). POSITION SUMMARY The Senior Contract Operations Excellence & PM Manager position is accountable for compliant and high quality management of GMA company-sponsored studies (both non and interventional), Investigator Initiated Research (IIR) and Investigator-Sponsored Collaborative Studies (ISCS) data acquisition projects, and Expanded Access Programs (EAPs) POSITION DUTIES & RESPONSIBILITIES Lead all aspects of clinical studies from planning to execution. Assigned studies include interventional, non-interventional and data acquisitions within Global Medical Affairs Oncology SBUOverall accountable for study management of assigned studies, serve as primary contact for CRO. Lead and manage multi-disciplinary cross functional team in all aspects of studies activities including but not limited to site start up, CRO/vendor selection and management, study-specific timelines and study executionCoordinate for fair market value assessment of study budgets; initiate and manage contracting process. Liaise with appropriate internal protocol review committees to ensure timely review, response and finalization of the protocol and protocol amendmentIIR and/or ISCS data acquisition projects. Responsibilities include chair conference calls, coordinate between team and IIR-sponsors on activities such as data review, query resolution and independent review of imaging scans, when applicable. Develop and manage overall project timelinesSupport GMA Medical Leads on overall delivery of the data generated from Oncology Non-Interventional Studies (NIS). Responsibilities include, but not limited to, monitor country/site selection and activation process, contribute in CRF design and review, study budget management, support Medical Leads on clinical data consistency review to ensure that data issues raised during medical and DM data review are adequately queried and resolvedManage study drug forecasting. Liaise with Clinical Supplies Management to ensure drug supply planning, labeling and distribution are executed timely and within applicable country and regional guidelinesAssist and/or lead in executing Expanded Access Programs within Oncology MA. Responsibilities include collaborate with country affiliates and Medical Experts as appropriate to ensure timely alignment and execution of country specific processes including permit license application, commercial product transition plan, and Real World Data (RWD) data generation when applicable  qualifications: SKILLS Extensive (7+ years) study management experience involving Phases 2 & 3 studies from planning through regulatory submission; regulatory submission experience a plusUnderstanding of the connection between protocol endpoints, study design, CRF design and data collection; clinical science backyard a plusAt least 5 years Oncology experience (can be outside of industry)Strong written, organizational, and computer (e.g. Excel, power point) skillsExcellent interpersonal and communication skills as candidate will interact with cross functional team members as well as liaise with external academic networks and cooperative groups from all over the global Preferences: Medical Affairs experience preferred REQUIREMENTS/PREFERENCES Education Requirement(s): Bachelor's degree required; life science preferredMasters in Science or Business Administration - preferred  skills: MS-EXCEL, Study Planning Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to find 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. We supply prestigious life sciences and biopharma companies with job seekers like you to achieve their business goals. If you're looking for a position where you can serve as an asset to your company while making a difference in others' lives, we have the ideal position for you!   location: Whippany, New Jersey job type: Contract salary: $42.85 - 50.41 per hour work hours: 8 to 4 education: Bachelors   responsibilities: This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation. DEPARTMENT/TEAM DESCRIPTION Operational Excellence and Project Management in Global Medical Affairs (GMA), Oncology SBU is a global function which partners and collaborates with the MA Teams and Key Stakeholders (internal and external) to assist in achieving short and long term strategic goals while adhering to "LIFE" values (leadership, integrity, flexibility, efficiency). POSITION SUMMARY The Senior Contract Operations Excellence & PM Manager position is accountable for compliant and high quality management of GMA company-sponsored studies (both non and interventional), Investigator Initiated Research (IIR) and Investigator-Sponsored Collaborative Studies (ISCS) data acquisition projects, and Expanded Access Programs (EAPs) POSITION DUTIES & RESPONSIBILITIES Lead all aspects of clinical studies from planning to execution. Assigned studies include interventional, non-interventional and data acquisitions within Global Medical Affairs Oncology SBUOverall accountable for study management of assigned studies, serve as primary contact for CRO. Lead and manage multi-disciplinary cross functional team in all aspects of studies activities including but not limited to site start up, CRO/vendor selection and management, study-specific timelines and study executionCoordinate for fair market value assessment of study budgets; initiate and manage contracting process. Liaise with appropriate internal protocol review committees to ensure timely review, response and finalization of the protocol and protocol amendmentIIR and/or ISCS data acquisition projects. Responsibilities include chair conference calls, coordinate between team and IIR-sponsors on activities such as data review, query resolution and independent review of imaging scans, when applicable. Develop and manage overall project timelinesSupport GMA Medical Leads on overall delivery of the data generated from Oncology Non-Interventional Studies (NIS). Responsibilities include, but not limited to, monitor country/site selection and activation process, contribute in CRF design and review, study budget management, support Medical Leads on clinical data consistency review to ensure that data issues raised during medical and DM data review are adequately queried and resolvedManage study drug forecasting. Liaise with Clinical Supplies Management to ensure drug supply planning, labeling and distribution are executed timely and within applicable country and regional guidelinesAssist and/or lead in executing Expanded Access Programs within Oncology MA. Responsibilities include collaborate with country affiliates and Medical Experts as appropriate to ensure timely alignment and execution of country specific processes including permit license application, commercial product transition plan, and Real World Data (RWD) data generation when applicable  qualifications: SKILLS Extensive (7+ years) study management experience involving Phases 2 & 3 studies from planning through regulatory submission; regulatory submission experience a plusUnderstanding of the connection between protocol endpoints, study design, CRF design and data collection; clinical science backyard a plusAt least 5 years Oncology experience (can be outside of industry)Strong written, organizational, and computer (e.g. Excel, power point) skillsExcellent interpersonal and communication skills as candidate will interact with cross functional team members as well as liaise with external academic networks and cooperative groups from all over the global Preferences: Medical Affairs experience preferred REQUIREMENTS/PREFERENCES Education Requirement(s): Bachelor's degree required; life science preferredMasters in Science or Business Administration - preferred  skills: MS-EXCEL, Study Planning Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • bridgewater, new jersey
    • contract
    • $40 - $45 per hour
    job summary: As the world's 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. Located in 100 countries, our longtime partner is known for being the world's largest producer of vaccines and for covering seven major therapeutic areas. To be a part of the science that is changing the world, apply now! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: Bridgewater, New Jersey job type: Contract salary: $40 - 45 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Perform the operational and tracking needs for the execution of the live field force monitoring of speaker programs and HCP interactions.This will include ensuring all required operational steps have been completed within a specified time frame and performing necessary follow up and escalation as needed on a timely basis.Will also perform the intake of various support items and reports from third party monitors and conduct quality reviews based on established internal standards and ensure proper retention in our internal Sharepoint sites.Perform transactional monitoring of records for compliance with Company policies for non-promotional HCP engagements/consulting arrangements, speaker program expenses, HCP meals expenses, expense reports and other relevant compliance areas as needed. Identify anomalies from the monitoring and independently investigate, concluded, and report issues/results clearly to the managers of the field force monitoring team.Create transactional testing scripts and monitoring procedures on an ad hoc basis for relevant compliance areas as needed.Combine data output from various systems to compile reports that will be utilized by the field force monitoring team for the monitoring selection process.Will utilize Microsoft Excel to conduct data analyses of large amounts of data pulled from various systems.Lead the execution of the weekly field force monitoring records review requests from various business partners.Lead the accurate tracking of monitoring observations and assist with the compilation of the monitoring results to business leadership on a quarterly and ad hoc basis.Will also assist with preparing presentations using charts and graphs in Microsoft PowerPoint.Maintain the field force monitoring team's Sharepoint site and relevant monitoring documentation.Report observations, remediation, and anomalies to the Lead Mandated Monitoring in a manner that leads to resolution.The individual will take on compliance monitoring projects on an ad hoc basis and interact with relevant areas of the business (commercial, medical, legal, regulatory, and/or business operations) and should have the ability to establish strong working relationships.The individual will execute the projects from start to finish with minimal supervision.This can include assisting with follow up with regulatory and legal required as a result of records review (i.e. emails, call notes, etc) promotional messaging content items flagged for review.  qualifications: Education - Bachelor's degree4-6 years of professional experience with 2 years of experience in pharmaceutical compliance (Preferred)Monitoring/Auditing/Quality experience or equivalentOrganized and detail oriented with a strong compliance mindsetSound written and verbal communication skillsExperienced in data analysisSound business acumen, analytical and problem-solving skills, and ability to present complex informationMust be proficient in Microsoft Excel, Word, and PowerPoint. Must be able to adjust to the changes in the business quickly in order to successfully navigate the various applications and systems.Be able to work independently with minimal supervision in a fast-paced environment and handle multiple tasks.  skills: MS-WORD, MS-EXCEL, MS-Powerpoint Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    job summary: As the world's 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. Located in 100 countries, our longtime partner is known for being the world's largest producer of vaccines and for covering seven major therapeutic areas. To be a part of the science that is changing the world, apply now! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: Bridgewater, New Jersey job type: Contract salary: $40 - 45 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Perform the operational and tracking needs for the execution of the live field force monitoring of speaker programs and HCP interactions.This will include ensuring all required operational steps have been completed within a specified time frame and performing necessary follow up and escalation as needed on a timely basis.Will also perform the intake of various support items and reports from third party monitors and conduct quality reviews based on established internal standards and ensure proper retention in our internal Sharepoint sites.Perform transactional monitoring of records for compliance with Company policies for non-promotional HCP engagements/consulting arrangements, speaker program expenses, HCP meals expenses, expense reports and other relevant compliance areas as needed. Identify anomalies from the monitoring and independently investigate, concluded, and report issues/results clearly to the managers of the field force monitoring team.Create transactional testing scripts and monitoring procedures on an ad hoc basis for relevant compliance areas as needed.Combine data output from various systems to compile reports that will be utilized by the field force monitoring team for the monitoring selection process.Will utilize Microsoft Excel to conduct data analyses of large amounts of data pulled from various systems.Lead the execution of the weekly field force monitoring records review requests from various business partners.Lead the accurate tracking of monitoring observations and assist with the compilation of the monitoring results to business leadership on a quarterly and ad hoc basis.Will also assist with preparing presentations using charts and graphs in Microsoft PowerPoint.Maintain the field force monitoring team's Sharepoint site and relevant monitoring documentation.Report observations, remediation, and anomalies to the Lead Mandated Monitoring in a manner that leads to resolution.The individual will take on compliance monitoring projects on an ad hoc basis and interact with relevant areas of the business (commercial, medical, legal, regulatory, and/or business operations) and should have the ability to establish strong working relationships.The individual will execute the projects from start to finish with minimal supervision.This can include assisting with follow up with regulatory and legal required as a result of records review (i.e. emails, call notes, etc) promotional messaging content items flagged for review.  qualifications: Education - Bachelor's degree4-6 years of professional experience with 2 years of experience in pharmaceutical compliance (Preferred)Monitoring/Auditing/Quality experience or equivalentOrganized and detail oriented with a strong compliance mindsetSound written and verbal communication skillsExperienced in data analysisSound business acumen, analytical and problem-solving skills, and ability to present complex informationMust be proficient in Microsoft Excel, Word, and PowerPoint. Must be able to adjust to the changes in the business quickly in order to successfully navigate the various applications and systems.Be able to work independently with minimal supervision in a fast-paced environment and handle multiple tasks.  skills: MS-WORD, MS-EXCEL, MS-Powerpoint Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • south plainfield, new jersey
    • contract
    • $40 - $45 per hour
    job summary: The Research Biologist is responsible for performing scientific experiments that contribute to Research and Drug discovery activities. This position assists in the conduct of early-stage research, the goal of which is the identification of New Chemical Entities (NCEs), as well as the advancement of research programs from the identification of screening hits to advanced lead optimization. The incumbent is also responsible for communicating experimental results to his/her supervisor and the project team.   location: South Plainfield, New Jersey job type: Contract salary: $40 - 45 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Under direct supervision, executes experiments and communicates results as part of multi-disciplinary team(s).Applies relevant scientific principles and techniques to research problems.Maintains detailed laboratory notebooks.Abides by all safety requirements.Ability to trouble shoot experimentsContributes to general laboratory needs/operation.Specific duties may also include, but may not be limited to, the following:Provides support for the characterization of compounds on different immune cells.Provides support for lead optimization by screening compounds and/or supporting structure activity relationship (SAR) studies involving the characterization of the biological activity of compounds in various assays. Profiles selected compounds in additional cells/assays.Provides support for in vitro studies as required.Assists in the development of biologically relevant preclinical animal models.  qualifications: Bachelor's degree in a scientific discipline with at least 3 years of research experience. Master's degree preferred.Hands-on experience in mammalian cell culture, and various cell-based assay technologies, such as CellTiterGlo, ELISA and HTRF.Knowledge of and ability to use standard cell biology and molecular biology techniques including western blotting, RT-PCR, qPCR and data analysis.Proficiency with Microsoft Office- preferably MS Excel and MS PowerPoint, and Graphpad Prism.Ability to work collaboratively under direct supervision, in a fast-paced, matrixed, team environment.Excellent planning, organization, and time management skills.Effective verbal and written communication and skills. Preferred: Experience performing transient and stable transfection, Lentiviral transduction, RNAi or CRISPR assays is desired.Compound screening in 96-well or 384-well format is a strong plus.?Immunofluorescence microscopy is a plus.  skills: Cell Biology, Cell Cultures Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    job summary: The Research Biologist is responsible for performing scientific experiments that contribute to Research and Drug discovery activities. This position assists in the conduct of early-stage research, the goal of which is the identification of New Chemical Entities (NCEs), as well as the advancement of research programs from the identification of screening hits to advanced lead optimization. The incumbent is also responsible for communicating experimental results to his/her supervisor and the project team.   location: South Plainfield, New Jersey job type: Contract salary: $40 - 45 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Under direct supervision, executes experiments and communicates results as part of multi-disciplinary team(s).Applies relevant scientific principles and techniques to research problems.Maintains detailed laboratory notebooks.Abides by all safety requirements.Ability to trouble shoot experimentsContributes to general laboratory needs/operation.Specific duties may also include, but may not be limited to, the following:Provides support for the characterization of compounds on different immune cells.Provides support for lead optimization by screening compounds and/or supporting structure activity relationship (SAR) studies involving the characterization of the biological activity of compounds in various assays. Profiles selected compounds in additional cells/assays.Provides support for in vitro studies as required.Assists in the development of biologically relevant preclinical animal models.  qualifications: Bachelor's degree in a scientific discipline with at least 3 years of research experience. Master's degree preferred.Hands-on experience in mammalian cell culture, and various cell-based assay technologies, such as CellTiterGlo, ELISA and HTRF.Knowledge of and ability to use standard cell biology and molecular biology techniques including western blotting, RT-PCR, qPCR and data analysis.Proficiency with Microsoft Office- preferably MS Excel and MS PowerPoint, and Graphpad Prism.Ability to work collaboratively under direct supervision, in a fast-paced, matrixed, team environment.Excellent planning, organization, and time management skills.Effective verbal and written communication and skills. Preferred: Experience performing transient and stable transfection, Lentiviral transduction, RNAi or CRISPR assays is desired.Compound screening in 96-well or 384-well format is a strong plus.?Immunofluorescence microscopy is a plus.  skills: Cell Biology, Cell Cultures Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • somerset, new jersey
    • temp to perm
    • $30 - $38 per hour
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to find 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. We supply prestigious life sciences and biopharma companies with job seekers like you to achieve their business goals. If you're looking for a position where you can serve as an asset to your company while making a difference in others' lives, we have the ideal position for you! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment.   location: Somerset, New Jersey job type: Temporary salary: $30 - 38 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Perform testing/review on incoming materials, in-process and finished products, and stability studies in QC Laboratory. Analytical : Utilize HPGe, HPLC, GC and other required equipment. Responsible for reserves and internal stability studies. Work with MTD and vendors on Reference Standard programs supporting commercial products. Microbiology : Familiar with aseptic technique. Perform bioburden, sterility tests in cleanroom BSCs. Perform Environmental Monitoring using EM Total Particulate/Viable monitors, and other required equipment/materials. Coordinate growth promotion/IDs. RESPONSIBILITIES Perform routine, non-routine and some advanced QC testing in accordance with SOPs and cGMP guidelines. Perform a wide variety of methods and utilize equipment ranging from basic to advanced. Limited supervision required.Perform verification of data to ensure accuracy. Perform approval upon discretion of supervisor.Assist with audit readiness of laboratory area and calibration and maintenance of laboratory equipment.Utilize a range of electronic systems such as document/equipment management software, LIMS, Empower, and ERP.Author and review SOP changes; participate in change controls, CAPAs and other quality systems.Resolve routine and some advanced problems by utilizing appropriate resources. Provide problem solving skills to support investigations.Participate in protocols for procedural and instrumentation validations. Work on special projects as needed. Contribute towards continuous improvement.Train on and maintain considerable knowledge of current regulatory requirements and relevant internal procedures.Work independently and as a team player with quality and attention to detail. Good communication skills both oral and written. Effectively and efficiently participate in assigned tasks in a quality manner.Actively promote safety rules and awareness. Report and take initiative to correct safety & environmental hazards. Work with potentially hazardous chemical, radiological and/or biological materials on a daily basis. Demonstrate good safety practices at all times including the appropriate use of protective equipment. Promote and actively demonstrate the values of Accountability, Quality, Efficiency, Customer Service, Collaboration, and Safety, as well as appropriate workplace behaviors and professionalism, including respect, flexibility, and a positive attitude toward work and others.  qualifications: Typically requires 3-5 years with a BS degree in a related scientific discipline (e.g. chemistry, biology) or equivalent combination of education and previous relevant experience in the pharmaceutical industry, related GMP environment, or equivalent.Routinely scheduled work may be required on evenings, weekends, and/or holidays, including during adverse weather conditions. Some non-routine travel may be required.Work with (or in proximity to) potentially hazardous chemical, radiological, and or biological materials and must be able to lift/move materials, e.g. portable equipment, lead, gas cylinders, bottles of chemicals/waste containers  skills: CAPA, GLP (Good Laboratory Practice), GMP (Good Manufacturing Practice) Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    job summary: As the world's largest staffing and recruitment agency in the world, we can commit to find 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. We supply prestigious life sciences and biopharma companies with job seekers like you to achieve their business goals. If you're looking for a position where you can serve as an asset to your company while making a difference in others' lives, we have the ideal position for you! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment.   location: Somerset, New Jersey job type: Temporary salary: $30 - 38 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Perform testing/review on incoming materials, in-process and finished products, and stability studies in QC Laboratory. Analytical : Utilize HPGe, HPLC, GC and other required equipment. Responsible for reserves and internal stability studies. Work with MTD and vendors on Reference Standard programs supporting commercial products. Microbiology : Familiar with aseptic technique. Perform bioburden, sterility tests in cleanroom BSCs. Perform Environmental Monitoring using EM Total Particulate/Viable monitors, and other required equipment/materials. Coordinate growth promotion/IDs. RESPONSIBILITIES Perform routine, non-routine and some advanced QC testing in accordance with SOPs and cGMP guidelines. Perform a wide variety of methods and utilize equipment ranging from basic to advanced. Limited supervision required.Perform verification of data to ensure accuracy. Perform approval upon discretion of supervisor.Assist with audit readiness of laboratory area and calibration and maintenance of laboratory equipment.Utilize a range of electronic systems such as document/equipment management software, LIMS, Empower, and ERP.Author and review SOP changes; participate in change controls, CAPAs and other quality systems.Resolve routine and some advanced problems by utilizing appropriate resources. Provide problem solving skills to support investigations.Participate in protocols for procedural and instrumentation validations. Work on special projects as needed. Contribute towards continuous improvement.Train on and maintain considerable knowledge of current regulatory requirements and relevant internal procedures.Work independently and as a team player with quality and attention to detail. Good communication skills both oral and written. Effectively and efficiently participate in assigned tasks in a quality manner.Actively promote safety rules and awareness. Report and take initiative to correct safety & environmental hazards. Work with potentially hazardous chemical, radiological and/or biological materials on a daily basis. Demonstrate good safety practices at all times including the appropriate use of protective equipment. Promote and actively demonstrate the values of Accountability, Quality, Efficiency, Customer Service, Collaboration, and Safety, as well as appropriate workplace behaviors and professionalism, including respect, flexibility, and a positive attitude toward work and others.  qualifications: Typically requires 3-5 years with a BS degree in a related scientific discipline (e.g. chemistry, biology) or equivalent combination of education and previous relevant experience in the pharmaceutical industry, related GMP environment, or equivalent.Routinely scheduled work may be required on evenings, weekends, and/or holidays, including during adverse weather conditions. Some non-routine travel may be required.Work with (or in proximity to) potentially hazardous chemical, radiological, and or biological materials and must be able to lift/move materials, e.g. portable equipment, lead, gas cylinders, bottles of chemicals/waste containers  skills: CAPA, GLP (Good Laboratory Practice), GMP (Good Manufacturing Practice) Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • pennington, new jersey
    • contract
    • $28 - $30 per hour
    job summary: The Contract, Laboratory Technician will adhere to both written procedures and verbal instructions. The incumbent will execute laboratory tasks with strict attention to safety and quality. Accurate and timely execution of activities and results are a requirement. Strict adherence to federal, state, and local regulations is mandatory. Collaborative work with research staff is a necessity to achieve departmental and company goals. Tasks will require working in laboratory areas using established procedures and SOPs. The incumbent works cross-functionally with internal departments and external resources on Laboratory and Instrument related issues.   location: Pennington, New Jersey job type: Contract salary: $28 - 30 per hour work hours: 9 to 5 education: Associate   responsibilities: Under general supervision, the position is responsible for a centralized stockroom and point of use areas for regular, and specialized Research and Development laboratory equipment, supplies, glassware, chemicals, and other related items.Monitors material levels in the centralized stockroom and within all CMC labs. Places orders as necessary, including on-demand orders in client order management system, as directed by research staff and Laboratory Manager.Label GxP materials appropriately according to the SOP with the received date.Review documentation upon receipt, unbox the materials and perform inspection. Report any compromise to the packaging integrity or item to management and Shipping & Receiving.Complies with all safety requirements.Contributes to general lab operations such as: Equipment maintenance.Identification of capital equipment needs.Maintenance of clean and uncluttered work areas.Maintain inventory and ordering lab supplies as needed. Performs other tasks and assignments as needed and specified by management.   qualifications: Associate degree or higher in a scientific discipline with a minimum of 2 years' experience in a laboratory setting or equivalent experience and/or education.Demonstrates technical proficiency, scientific creativity, and the ability to collaborate with others on cross functional teams in a fast-paced, matrixed, environment consisting of internal and external team members. Laboratory experience in Biologics and/or R&D.Knowledge of GxP documentation.Proficiency in SAP, and Oracle applications.Proficiency with Microsoft Office.Excellent verbal and written communication and skills.Ability to work independently and collaboratively, as required, in a fast-paced, matrixed, team environment consisting of internal and external team members.Analytical thinker with excellent problem solving skills and the ability to adapt to changing priorities and deadlines. Excellent planning, organization and time management skills including the ability to support and prioritize multiple projects. Preferred: GxP knowledge.Seasoned background in 5S Methodology.Basic equipment troubleshooting.  skills: GMP (Good Manufacturing Practice), Sample Preparation, Sanitation Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    job summary: The Contract, Laboratory Technician will adhere to both written procedures and verbal instructions. The incumbent will execute laboratory tasks with strict attention to safety and quality. Accurate and timely execution of activities and results are a requirement. Strict adherence to federal, state, and local regulations is mandatory. Collaborative work with research staff is a necessity to achieve departmental and company goals. Tasks will require working in laboratory areas using established procedures and SOPs. The incumbent works cross-functionally with internal departments and external resources on Laboratory and Instrument related issues.   location: Pennington, New Jersey job type: Contract salary: $28 - 30 per hour work hours: 9 to 5 education: Associate   responsibilities: Under general supervision, the position is responsible for a centralized stockroom and point of use areas for regular, and specialized Research and Development laboratory equipment, supplies, glassware, chemicals, and other related items.Monitors material levels in the centralized stockroom and within all CMC labs. Places orders as necessary, including on-demand orders in client order management system, as directed by research staff and Laboratory Manager.Label GxP materials appropriately according to the SOP with the received date.Review documentation upon receipt, unbox the materials and perform inspection. Report any compromise to the packaging integrity or item to management and Shipping & Receiving.Complies with all safety requirements.Contributes to general lab operations such as: Equipment maintenance.Identification of capital equipment needs.Maintenance of clean and uncluttered work areas.Maintain inventory and ordering lab supplies as needed. Performs other tasks and assignments as needed and specified by management.   qualifications: Associate degree or higher in a scientific discipline with a minimum of 2 years' experience in a laboratory setting or equivalent experience and/or education.Demonstrates technical proficiency, scientific creativity, and the ability to collaborate with others on cross functional teams in a fast-paced, matrixed, environment consisting of internal and external team members. Laboratory experience in Biologics and/or R&D.Knowledge of GxP documentation.Proficiency in SAP, and Oracle applications.Proficiency with Microsoft Office.Excellent verbal and written communication and skills.Ability to work independently and collaboratively, as required, in a fast-paced, matrixed, team environment consisting of internal and external team members.Analytical thinker with excellent problem solving skills and the ability to adapt to changing priorities and deadlines. Excellent planning, organization and time management skills including the ability to support and prioritize multiple projects. Preferred: GxP knowledge.Seasoned background in 5S Methodology.Basic equipment troubleshooting.  skills: GMP (Good Manufacturing Practice), Sample Preparation, Sanitation Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    • somerville, new jersey
    • contract
    • $35 - $40.66 per hour
    job summary: As the world's 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 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! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: Somerville, New Jersey job type: Contract salary: $35.00 - 40.66 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Conduct laboratory experiments to generate reliable and consistent data in a timely manner.Document, discuss, and modify experimental studies as needed in collaboration with other team members and/or project lead.Summarize data and assist project lead in maintaining project documentation.  qualifications: Bachelor degree in mechanical engineering, material science, biomedical engineering or a related field with 1+ years of academic or industry laboratory experienceExperience with performing and troubleshooting a wide variety of material characterization assays is desiredDemonstrated ability to quickly learn new concepts, skills and techniquesCapable of contributing independently but also work successfully in a highly collaborative scientific environmentPossess strong written and oral communication skillsWorking knowledge of MS Office (Excel, Word, PowerPoint) and basic understanding of statistical analyses is a plusMeticulous attention to detail and diligence in record keeping  skills: MS-WORD, MS-EXCEL, MS-Powerpoint, Biology, GLP (Good Laboratory Practice), GMP (Good Manufacturing Practice) Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.
    job summary: As the world's 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 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! This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   location: Somerville, New Jersey job type: Contract salary: $35.00 - 40.66 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Conduct laboratory experiments to generate reliable and consistent data in a timely manner.Document, discuss, and modify experimental studies as needed in collaboration with other team members and/or project lead.Summarize data and assist project lead in maintaining project documentation.  qualifications: Bachelor degree in mechanical engineering, material science, biomedical engineering or a related field with 1+ years of academic or industry laboratory experienceExperience with performing and troubleshooting a wide variety of material characterization assays is desiredDemonstrated ability to quickly learn new concepts, skills and techniquesCapable of contributing independently but also work successfully in a highly collaborative scientific environmentPossess strong written and oral communication skillsWorking knowledge of MS Office (Excel, Word, PowerPoint) and basic understanding of statistical analyses is a plusMeticulous attention to detail and diligence in record keeping  skills: MS-WORD, MS-EXCEL, MS-Powerpoint, Biology, GLP (Good Laboratory Practice), GMP (Good Manufacturing Practice) Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com. For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information.

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