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    • tampa, florida
    • temp to perm
    • $23 per hour
    Do you have experience as a Lab Analyst? Are you knowledgeable in the water filtration manufacturing field? You can use both of those skills in this Lab Analyst position. Randstad Pinellas is currently recruiting for Lab Analyst opportunity at a manufacturing company in Oldsmar, FL. It is a fast-paced environment with a professional team. Position is in Oldsmar, FL. $23.00/Hour-1st Shift Available 7am - 3:30pm M-F Candidates must have: 1-5 years of experience in a lab Chemistry, Biology or related degree Analytical Chemistry experience General Maintenance skills (plumbing, electrical, etc.) a PLUS! Ability to work overtime Please apply online now and attach your resume!salary: $23 - $23 per hourshift: Firstwork hours: 7 AM - 3:30 PMeducation: BachelorResponsibilities Perform procedures and provide reports on testing. This may include: Providing guidance on selecting, purchasing, and setting up test equipment. Taking samples and running chemical and/or physical analysis on samples. Recording and interpreting data in a useful format. Sending reports and explaining results to customers and others in the organization. Maintain and stock the lab. Including but not limited to the following specific responsibilities: Perform minor maintenance activities. Note and report equipment needing repair. Perform equipment calibrations and schedule recalibrations. Assist in ordering chemicals and materials. Assist in maintaining SDSs for chemicals used in the lab. Manage the completed test sample storage area. Write and modify lab procedures based on NSF/ANSI standards and/or customer requests. A chemistry, biology, or related degree and/or 1-5 years laboratory experience.  Analytical chemistry experience preferred. The essential functions of this role include:manual lifting up to 40lbsSkillsLaboratory/Sciences (5 years of experience is preferred)AnalysisNSF/ANSI standardsQualificationsYears of experience: 5 yearsExperience level: ExperiencedRandstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad. 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. 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.
    Do you have experience as a Lab Analyst? Are you knowledgeable in the water filtration manufacturing field? You can use both of those skills in this Lab Analyst position. Randstad Pinellas is currently recruiting for Lab Analyst opportunity at a manufacturing company in Oldsmar, FL. It is a fast-paced environment with a professional team. Position is in Oldsmar, FL. $23.00/Hour-1st Shift Available 7am - 3:30pm M-F Candidates must have: 1-5 years of experience in a lab Chemistry, Biology or related degree Analytical Chemistry experience General Maintenance skills (plumbing, electrical, etc.) a PLUS! Ability to work overtime Please apply online now and attach your resume!salary: $23 - $23 per hourshift: Firstwork hours: 7 AM - 3:30 PMeducation: BachelorResponsibilities Perform procedures and provide reports on testing. This may include: Providing guidance on selecting, purchasing, and setting up test equipment. Taking samples and running chemical and/or physical analysis on samples. Recording and interpreting data in a useful format. Sending reports and explaining results to customers and others in the organization. Maintain and stock the lab. Including but not limited to the following specific responsibilities: Perform minor maintenance activities. Note and report equipment needing repair. Perform equipment calibrations and schedule recalibrations. Assist in ordering chemicals and materials. Assist in maintaining SDSs for chemicals used in the lab. Manage the completed test sample storage area. Write and modify lab procedures based on NSF/ANSI standards and/or customer requests. A chemistry, biology, or related degree and/or 1-5 years laboratory experience.  Analytical chemistry experience preferred. The essential functions of this role include:manual lifting up to 40lbsSkillsLaboratory/Sciences (5 years of experience is preferred)AnalysisNSF/ANSI standardsQualificationsYears of experience: 5 yearsExperience level: ExperiencedRandstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad. 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. 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.
    • daytona beach, florida
    • contract
    • $57.18 - $67.27 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: Daytona Beach, Florida job type: Contract salary: $57.18 - 67.27 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Job Responsibilities The main function of a regional CRA is to perform complex medical laboratory tests for the diagnosis, treatment and prevention of disease. Site monitoring responsibility for clinical studies according to Standard Operating Procedures, ICH Guidelines and GCPSite management responsibility for clinical studies according to Covance Standard Operating Procedures, ICH Guidelines and GCPAssures the implementation of project plans as assignedFunction as leader for projects of limited scope as assignedAssume line management responsibilities as assignedAct in the project role of a Local Project Coordinator or Lead CRA as assignedResponsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assignedResponsible for all aspects of site management as prescribed in the project plans General On-Site Monitoring Responsibilities Ensure the study staff who will conduct the protocol have received the proper materials and instructions to safely enter patients into the studyEnsure the protection of study patients by verifying that informed consent procedures and protocol requirements are adhered to according to the applicable regulatory requirementsEnsure the integrity of the data submitted on Case Report Forms (CRFs) or other data collection tools by careful source document reviewMonitor data for missing or implausible dataEnsure the resources of the Sponsor and Covance are spent wisely by performing the required monitoring tasks in an efficient manner, according to SOPs and established guidelines, including managing travel expenses in an economical fashion according to Covance travel policyTravel, including air travel, may be required and is an essential function of the job.Prepare accurate and timely trip reportsManage small projects under direction of a Project Manager/Director as assignedServe as lead monitor for a protocol or project, and may assist in establishing monitoring plans and trip report review as assignedReview progress of projects and initiate appropriate actions to achieve target objectivesOrganize and make presentations at Investigator MeetingsParticipate in the development of protocols and Case Report Forms as assignedParticipate in writing clinical trial reports as assignedInteract with internal work groups to evaluate needs, resources and timelinesAct as contact for clinical trial supplies and other suppliers (vendors) as assignedResponsible for all aspects of registry management as prescribed in the project plansUndertake feasibility work when requestedConduct, report and follow-up on Quality Control Visits (CQC) when requestedRecruitment of potential investigators, preparation of EC submissions, notifications to regulatory authorities, translation of study-related documentation, organization of meetings and other tasks as instructed by supervisor as assignedNegotiate study budgets with potential investigators and assist the Covance legal department with statements of agreements as assignedComplete process of Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAEsIndependently perform CRF review; query generation and resolution against established data review guidelines on data management systems as assigned by managementAssist with training, mentoring and development of new employees, e.g. co-monitoringCoordinate designated clinical projects as a Local Project Coordinator (with supervision, if applicable), and may act as a local client contact as assigned  qualifications: Skills: Verbal and written communication skills, attention to detail, and problem solving skills.Expert ability to work independently and manage ones time.Expert leadership and mentoring skills necessary to provide support and constructive performance feedback.Expert knowledge of Good Clinical Practice (international quality standard for human clinical trials) and local regulations.Expert knowledge of the information and techniques needed to diagnose and treat human injuries and diseases.Expert ability to analyze data and accurately document and record results Education & Qualifications Bachelor's degree in life sciences or related field required. 3+ years experience required.  skills: SOP, GCP (Good Clinical 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!   location: Daytona Beach, Florida job type: Contract salary: $57.18 - 67.27 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Job Responsibilities The main function of a regional CRA is to perform complex medical laboratory tests for the diagnosis, treatment and prevention of disease. Site monitoring responsibility for clinical studies according to Standard Operating Procedures, ICH Guidelines and GCPSite management responsibility for clinical studies according to Covance Standard Operating Procedures, ICH Guidelines and GCPAssures the implementation of project plans as assignedFunction as leader for projects of limited scope as assignedAssume line management responsibilities as assignedAct in the project role of a Local Project Coordinator or Lead CRA as assignedResponsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assignedResponsible for all aspects of site management as prescribed in the project plans General On-Site Monitoring Responsibilities Ensure the study staff who will conduct the protocol have received the proper materials and instructions to safely enter patients into the studyEnsure the protection of study patients by verifying that informed consent procedures and protocol requirements are adhered to according to the applicable regulatory requirementsEnsure the integrity of the data submitted on Case Report Forms (CRFs) or other data collection tools by careful source document reviewMonitor data for missing or implausible dataEnsure the resources of the Sponsor and Covance are spent wisely by performing the required monitoring tasks in an efficient manner, according to SOPs and established guidelines, including managing travel expenses in an economical fashion according to Covance travel policyTravel, including air travel, may be required and is an essential function of the job.Prepare accurate and timely trip reportsManage small projects under direction of a Project Manager/Director as assignedServe as lead monitor for a protocol or project, and may assist in establishing monitoring plans and trip report review as assignedReview progress of projects and initiate appropriate actions to achieve target objectivesOrganize and make presentations at Investigator MeetingsParticipate in the development of protocols and Case Report Forms as assignedParticipate in writing clinical trial reports as assignedInteract with internal work groups to evaluate needs, resources and timelinesAct as contact for clinical trial supplies and other suppliers (vendors) as assignedResponsible for all aspects of registry management as prescribed in the project plansUndertake feasibility work when requestedConduct, report and follow-up on Quality Control Visits (CQC) when requestedRecruitment of potential investigators, preparation of EC submissions, notifications to regulatory authorities, translation of study-related documentation, organization of meetings and other tasks as instructed by supervisor as assignedNegotiate study budgets with potential investigators and assist the Covance legal department with statements of agreements as assignedComplete process of Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAEsIndependently perform CRF review; query generation and resolution against established data review guidelines on data management systems as assigned by managementAssist with training, mentoring and development of new employees, e.g. co-monitoringCoordinate designated clinical projects as a Local Project Coordinator (with supervision, if applicable), and may act as a local client contact as assigned  qualifications: Skills: Verbal and written communication skills, attention to detail, and problem solving skills.Expert ability to work independently and manage ones time.Expert leadership and mentoring skills necessary to provide support and constructive performance feedback.Expert knowledge of Good Clinical Practice (international quality standard for human clinical trials) and local regulations.Expert knowledge of the information and techniques needed to diagnose and treat human injuries and diseases.Expert ability to analyze data and accurately document and record results Education & Qualifications Bachelor's degree in life sciences or related field required. 3+ years experience required.  skills: SOP, GCP (Good Clinical 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.
    • jacksonville, florida
    • temp to perm
    • $17 per hour
    Randstad is looking for an experienced quality assurance inspector for a temporary to hire position on the Southside of Jacksonville. You will perform the finished parts/products examination and inspection process, and ensure conformance by utilizing the controlled procedures with inspection tasks, product description, and reference materials. The starting pay will be $17 per hour. salary: $17 - $17 per hourshift: Firstwork hours: 9 AM - 6 PMeducation: High` SchoolResponsibilities Performs finished parts and product examination and inspections to standards. Has knowledge of metric system and is capable of using measurement equipment on inspection material. Has knowledge and complies with the sampling process. Assists with the compliance of the Unique Device Identification (UDI) System Communicates and assists with nonconforming material Entries documented and tracked in SAP. Contributes and assists with process improvement initiatives Assures quality assurance areas are kept in a clean, safe, and orderly manner. Performs other related duties as assigned The essential functions of this role include:working in a smoke free environmentstanding for 8 hours at one timeSkillsQuality AssuranceQuality ControlProduct InspectionFirst Yield PassSamplingTestingInspectionProduction ControlMonitoringProviding FeedbackSortingQualificationsYears of experience: 1 yearExperience level: ExperiencedRandstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad. 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. 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.
    Randstad is looking for an experienced quality assurance inspector for a temporary to hire position on the Southside of Jacksonville. You will perform the finished parts/products examination and inspection process, and ensure conformance by utilizing the controlled procedures with inspection tasks, product description, and reference materials. The starting pay will be $17 per hour. salary: $17 - $17 per hourshift: Firstwork hours: 9 AM - 6 PMeducation: High` SchoolResponsibilities Performs finished parts and product examination and inspections to standards. Has knowledge of metric system and is capable of using measurement equipment on inspection material. Has knowledge and complies with the sampling process. Assists with the compliance of the Unique Device Identification (UDI) System Communicates and assists with nonconforming material Entries documented and tracked in SAP. Contributes and assists with process improvement initiatives Assures quality assurance areas are kept in a clean, safe, and orderly manner. Performs other related duties as assigned The essential functions of this role include:working in a smoke free environmentstanding for 8 hours at one timeSkillsQuality AssuranceQuality ControlProduct InspectionFirst Yield PassSamplingTestingInspectionProduction ControlMonitoringProviding FeedbackSortingQualificationsYears of experience: 1 yearExperience level: ExperiencedRandstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad. 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. 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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