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    • rockville, maryland
    • temp to perm
    • $25 - $28.84 per hour
    Randstad is seeking several  Associate Scientists for a major life science organization. This client is the North American life science brand of a major German based biotech/pharma organization – a leading science and technology company. It offers a broad range of innovative products and services to biotech and pharmaceutical drug therapies businesses. Through dedicated collaboration with the scientific and engineering communities, and as one of the top three R&D investors in the life science tools industry, the brand serves as a strategic partner to customers and helps advance the promise of life science.  These are 4-8 month contract to permanent hire opportunities for both Associate Scientist level I and II!We'll be hosting virtual Career Fairs on July 6th, 7th & 13th! We are looking to hire for both 1st & 2nd shift; some roles may require weekend work.salary: $25 - $28.84 per hourshift: First & Secondwork hours: 8 AM - 4 PM or 3 PM- 11PMeducation: BachelorYour Role:Perform assays/ testing for a laboratory within Biologics. This position does not have supervisory responsibilities.PURPOSE OF THE POSITIONThe Associate Scientist will perform safety testing required to manufacture clinical and commercial products. The AS is required to make scientific observations, maintain detailed workbooks/documentation and ensure all documentation fulfills generally accepted professional/industry standards. Additionally, they are required to maintain a thorough understanding of BioReliance services, technical principles and applications.ESSENTIAL JOB FUNCTIONS Conducts assigned testing with minimal supervision within constraints of lab scheduling.Performs testing in accordance with SOPs and regulations (cGMP and GLP).Maintains complete and comprehensive records for study integrity.Makes detailed observations and documents results.Operates and maintains lab equipment as required by SOPs and testing procedures.Performs peer review of assay batch/lab records to ensure Right First Time (RFT)Utilizes applicable computer programs during testing and routine tasks (i.e. Word, Excel, Oracle, LIMS, BRIQS, etc.).Utilizes problem solving/ trouble shooting skills.Communicates deviations/ events, progress and interim results to Study Management.Informs supervisor of deviations or factors that may affect quality and accuracy of data.Maintains a working knowledge of lab procedures and assays.Assists with revisions to SOPs, laboratory records and other documentation as assigned.Complies with company health and safety regulations and procedures.Performs other duties as assigned. BASIC QUALIFICATIONSEducation (minimum requirements): BA/BS in scientific discipline with 0-2 years or relevant experienceOr equivalent relevant experience Experience: Experience with relevant laboratory practices, techniques, equipment, materials and mathematical calculations. Knowledge and Skills: Basic skills in applicable computer programsGood oral and written communication skillsWorks well in a team based environmentPCR (1 year of experience is preferred)qPCRAsceptic Techniques (1 year of experience is preferred)ELISA (1 year of experience is preferred) Qualifications Years of experience: 1 yearExperience level: Entry Level Randstad 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 seeking several  Associate Scientists for a major life science organization. This client is the North American life science brand of a major German based biotech/pharma organization – a leading science and technology company. It offers a broad range of innovative products and services to biotech and pharmaceutical drug therapies businesses. Through dedicated collaboration with the scientific and engineering communities, and as one of the top three R&D investors in the life science tools industry, the brand serves as a strategic partner to customers and helps advance the promise of life science.  These are 4-8 month contract to permanent hire opportunities for both Associate Scientist level I and II!We'll be hosting virtual Career Fairs on July 6th, 7th & 13th! We are looking to hire for both 1st & 2nd shift; some roles may require weekend work.salary: $25 - $28.84 per hourshift: First & Secondwork hours: 8 AM - 4 PM or 3 PM- 11PMeducation: BachelorYour Role:Perform assays/ testing for a laboratory within Biologics. This position does not have supervisory responsibilities.PURPOSE OF THE POSITIONThe Associate Scientist will perform safety testing required to manufacture clinical and commercial products. The AS is required to make scientific observations, maintain detailed workbooks/documentation and ensure all documentation fulfills generally accepted professional/industry standards. Additionally, they are required to maintain a thorough understanding of BioReliance services, technical principles and applications.ESSENTIAL JOB FUNCTIONS Conducts assigned testing with minimal supervision within constraints of lab scheduling.Performs testing in accordance with SOPs and regulations (cGMP and GLP).Maintains complete and comprehensive records for study integrity.Makes detailed observations and documents results.Operates and maintains lab equipment as required by SOPs and testing procedures.Performs peer review of assay batch/lab records to ensure Right First Time (RFT)Utilizes applicable computer programs during testing and routine tasks (i.e. Word, Excel, Oracle, LIMS, BRIQS, etc.).Utilizes problem solving/ trouble shooting skills.Communicates deviations/ events, progress and interim results to Study Management.Informs supervisor of deviations or factors that may affect quality and accuracy of data.Maintains a working knowledge of lab procedures and assays.Assists with revisions to SOPs, laboratory records and other documentation as assigned.Complies with company health and safety regulations and procedures.Performs other duties as assigned. BASIC QUALIFICATIONSEducation (minimum requirements): BA/BS in scientific discipline with 0-2 years or relevant experienceOr equivalent relevant experience Experience: Experience with relevant laboratory practices, techniques, equipment, materials and mathematical calculations. Knowledge and Skills: Basic skills in applicable computer programsGood oral and written communication skillsWorks well in a team based environmentPCR (1 year of experience is preferred)qPCRAsceptic Techniques (1 year of experience is preferred)ELISA (1 year of experience is preferred) Qualifications Years of experience: 1 yearExperience level: Entry Level Randstad 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.
    • rockville, maryland
    • contract
    • $45 - $50 per hour
    job summary: The Analytical Development Scientist is responsible for in-process sample testing, for Manufacturing upstream and downstream as well as process development studies. Develops, plans, and performs analytical methods, (such as PCR based assays, protein determination, SDS-PAGE, Western Blot, ELISA, Endotoxin, and cell-based assays)   location: Rockville, Maryland job type: Contract salary: $45 - 50 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Perform Analytical Development Laboratory testing accurately, record all data, observations, and QC results accurately. Provide scientific input and demonstrate critical thinking in experimental design and execution.Perform analytical methods such as PCR-based assays (Traditional PCR, qPCR), protein determination by A 280, Bradford, and BCA, SDS-PAGE, Western Blot, ELISA, Endotoxin.Maintain cell cultures and generate analytical cell banks. Perform cell-based assays (TCID 50 , Plaque) as needed.Troubleshoot methods, compile, review and submit accurate reports. Compile and summarize test data and perform data analysis. Write essays, technical development reports and give oral presentations of data at internal or external meetings.Coordinate with other functional groups to support upstream and downstream, process development studies to meet corporate objectives.Write, review and edit SOPs and Test Methods for new procedures and assays; review, edit and revise existing SOPs to reflect changes in procedures.Order and maintain laboratory reagents and supplies.Responsible for following Good Documentation Practices (GDP) and ensuring adherence to current Good Manufacturing Practices (cGMP) compliance, and any other local, state, and federal regulations associated with the release of investigational and pharmaceutical drug products.Communicate matters of importance such as plans, technical problems, results, etc. to the manager/supervisor and to other scientific personnel associated with the study, which may impact the successful completion of projects.Ensures that all laboratory equipment is monitored for adherence to performance parameters on a scheduled basis and is operating within requirements. Immediately reports any equipment failures to management. Ordering new supplies and making sure that we do not run out of important reagents.Other duties as assigned  qualifications: Job Requirements Bachelor's degreeA minimum of 4-6 years of laboratory experienceMust possess a basic knowledge of molecular biology, virology, and cell biology techniques such as experience using real-time PCR, or performing various molecular assays.Must have strong experience in the development and performance of Cell-based assays and PCR-based assays (TCID 50 , Plaque, Traditional PCR, qPCR, etc.)Hands-on experience with non-cell-based analytical assays, including but not limited to: protein determination, SDS-PAGE, Western Blot, ELISA, pH, Endotoxin. Knowledge of cell culture and cell-based assays (TCID 50 , Plaque).Experience with the development and validation of assays used for the characterization of biological products (protein, antibody, VLP, AAV, live virus, etc).High attention to detail, excellent organizational skills, and the ability to work on multiple projects with tight deadlines.Demonstrated ability to work independently as well as a strong contributor in a cross-functional team environment on complex projects. Able to work effectively alone and in teams.Able to prioritize and demonstrate flexibility in schedule (late shift) as demanded by project needs or management.Requires excellent written and oral communication skills. Proven and demonstrated computer (PC) and software skills including MS Word, Excel, and PowerPoint are required.Willingness to cross-train as neededGreat interpersonal skillsStrong communicationTakes initiativeRemains calm under pressure  skills: Molecular Biology, Cell Biology, PCR 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.
    job summary: The Analytical Development Scientist is responsible for in-process sample testing, for Manufacturing upstream and downstream as well as process development studies. Develops, plans, and performs analytical methods, (such as PCR based assays, protein determination, SDS-PAGE, Western Blot, ELISA, Endotoxin, and cell-based assays)   location: Rockville, Maryland job type: Contract salary: $45 - 50 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Perform Analytical Development Laboratory testing accurately, record all data, observations, and QC results accurately. Provide scientific input and demonstrate critical thinking in experimental design and execution.Perform analytical methods such as PCR-based assays (Traditional PCR, qPCR), protein determination by A 280, Bradford, and BCA, SDS-PAGE, Western Blot, ELISA, Endotoxin.Maintain cell cultures and generate analytical cell banks. Perform cell-based assays (TCID 50 , Plaque) as needed.Troubleshoot methods, compile, review and submit accurate reports. Compile and summarize test data and perform data analysis. Write essays, technical development reports and give oral presentations of data at internal or external meetings.Coordinate with other functional groups to support upstream and downstream, process development studies to meet corporate objectives.Write, review and edit SOPs and Test Methods for new procedures and assays; review, edit and revise existing SOPs to reflect changes in procedures.Order and maintain laboratory reagents and supplies.Responsible for following Good Documentation Practices (GDP) and ensuring adherence to current Good Manufacturing Practices (cGMP) compliance, and any other local, state, and federal regulations associated with the release of investigational and pharmaceutical drug products.Communicate matters of importance such as plans, technical problems, results, etc. to the manager/supervisor and to other scientific personnel associated with the study, which may impact the successful completion of projects.Ensures that all laboratory equipment is monitored for adherence to performance parameters on a scheduled basis and is operating within requirements. Immediately reports any equipment failures to management. Ordering new supplies and making sure that we do not run out of important reagents.Other duties as assigned  qualifications: Job Requirements Bachelor's degreeA minimum of 4-6 years of laboratory experienceMust possess a basic knowledge of molecular biology, virology, and cell biology techniques such as experience using real-time PCR, or performing various molecular assays.Must have strong experience in the development and performance of Cell-based assays and PCR-based assays (TCID 50 , Plaque, Traditional PCR, qPCR, etc.)Hands-on experience with non-cell-based analytical assays, including but not limited to: protein determination, SDS-PAGE, Western Blot, ELISA, pH, Endotoxin. Knowledge of cell culture and cell-based assays (TCID 50 , Plaque).Experience with the development and validation of assays used for the characterization of biological products (protein, antibody, VLP, AAV, live virus, etc).High attention to detail, excellent organizational skills, and the ability to work on multiple projects with tight deadlines.Demonstrated ability to work independently as well as a strong contributor in a cross-functional team environment on complex projects. Able to work effectively alone and in teams.Able to prioritize and demonstrate flexibility in schedule (late shift) as demanded by project needs or management.Requires excellent written and oral communication skills. Proven and demonstrated computer (PC) and software skills including MS Word, Excel, and PowerPoint are required.Willingness to cross-train as neededGreat interpersonal skillsStrong communicationTakes initiativeRemains calm under pressure  skills: Molecular Biology, Cell Biology, PCR 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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