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8 jobs found in rockville, maryland

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    • sterling, virginia
    • permanent
    • $24 - $30 per year
    Ready to let your ambition thrive? We are looking for a candidate with previous leadership experience within a fast-paced environment. In this role, you will be responsible for ensuring the production of quality control through production, operations, and manufacturing. This is a position with hands-on responsibility and accountability for daily production flow and bottom-line results.  salary: $24 - $30 per yearshift: Firstwork hours: 4 AM - 12 PMeducation: BachelorResponsibilitieso Ensure all materials/reagents are accepted according to SOPs and within expiry, o Ensure all equipment is appropriately qualified prior to use o Operate the synthesis unit according to SOPs o Learn the basic operational principles of the synthesis unit and assist in routine maintenance of the synthesis unit  Perform FDG and NaF quality control (QC) processes according to SOPs: o Assist with basic maintenance of QC equipment o Ensure all equipment is appropriately calibrated and qualified prior to using o Operate the QC equipment according to SOPs  Ensure completion of applicable cGMP documentation.  Assist with inventory managementThe essential functions of this role include:manual lifting up to 50lbsstanding for 4 hours at one timeSkillsProduction ControlQuality AssuranceQuality ControlCoachingProviding FeedbackOperationsTestingQualificationsYears of experience: 2 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.EOEDisclaime 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.
    Ready to let your ambition thrive? We are looking for a candidate with previous leadership experience within a fast-paced environment. In this role, you will be responsible for ensuring the production of quality control through production, operations, and manufacturing. This is a position with hands-on responsibility and accountability for daily production flow and bottom-line results.  salary: $24 - $30 per yearshift: Firstwork hours: 4 AM - 12 PMeducation: BachelorResponsibilitieso Ensure all materials/reagents are accepted according to SOPs and within expiry, o Ensure all equipment is appropriately qualified prior to use o Operate the synthesis unit according to SOPs o Learn the basic operational principles of the synthesis unit and assist in routine maintenance of the synthesis unit  Perform FDG and NaF quality control (QC) processes according to SOPs: o Assist with basic maintenance of QC equipment o Ensure all equipment is appropriately calibrated and qualified prior to using o Operate the QC equipment according to SOPs  Ensure completion of applicable cGMP documentation.  Assist with inventory managementThe essential functions of this role include:manual lifting up to 50lbsstanding for 4 hours at one timeSkillsProduction ControlQuality AssuranceQuality ControlCoachingProviding FeedbackOperationsTestingQualificationsYears of experience: 2 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.EOEDisclaime 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.
    • sterling, virginia
    • permanent
    • $43,500 - $54,000 per year
    Would you like to work for a company that is committed to their employees’ safety and where you will be recognized for your contributions? We are looking for Pharmacy Techs to join an innovative company in the Sterling, VA area. If you can ensure the safe and efficient work environment  we have the job for you!salary: $43,500 - $54,000 per yearshift: Thirdwork hours: 3 PM - 11 AMeducation: AssociateResponsibilitiesPerform the duties associated with compounding, dispensing, and distribution of FDG and NaF, including data entry with Pinestar for end-of-day reports and daily dose management reports.  Ensure compliance with USP,  proposed regulations, or other state pharmacy requirements as applicable, at the site level; maintain a personal license in good standing through applicable state laws.  Complete cGMP documents as required within SOFIE’s Quality Management System.  Ensure aseptic operations follow internal procedures (gowning, cleaning/sanitation, sterility, environmental monitoring, etc.), customer requirements, and FDA regulations.  Maintain a clean and safe working environment.The essential functions of this role include:manual lifting up to 50lbsSkillsTestingInventoryQuality ControlSanitationQualificationsYears of experience: 3 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.EOEDisclaime 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.
    Would you like to work for a company that is committed to their employees’ safety and where you will be recognized for your contributions? We are looking for Pharmacy Techs to join an innovative company in the Sterling, VA area. If you can ensure the safe and efficient work environment  we have the job for you!salary: $43,500 - $54,000 per yearshift: Thirdwork hours: 3 PM - 11 AMeducation: AssociateResponsibilitiesPerform the duties associated with compounding, dispensing, and distribution of FDG and NaF, including data entry with Pinestar for end-of-day reports and daily dose management reports.  Ensure compliance with USP,  proposed regulations, or other state pharmacy requirements as applicable, at the site level; maintain a personal license in good standing through applicable state laws.  Complete cGMP documents as required within SOFIE’s Quality Management System.  Ensure aseptic operations follow internal procedures (gowning, cleaning/sanitation, sterility, environmental monitoring, etc.), customer requirements, and FDA regulations.  Maintain a clean and safe working environment.The essential functions of this role include:manual lifting up to 50lbsSkillsTestingInventoryQuality ControlSanitationQualificationsYears of experience: 3 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.EOEDisclaime 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
    • $20.40 - $24 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. Focusing on immune diseases like HIV that affect a large percentage of the population, the work our longtime partner conducts is imperative to a better, healthier future. To be recognized as a crucial part to furthering this goal, join this growing team 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: Rockville, Maryland job type: Contract salary: $20.40 - 24.00 per hour work hours: 9 to 5 education: Bachelors   responsibilities: - Being able to work a flexible shift schedule which includes coverage every other weekend. Includes possible placement on AM or PM shifts. - Completing daily manufacturing tasks per cGMPs, standard operating procedures, and batch document instructions - Monitoring critical process parameters - Documenting all manufacturing activities clearly and accurately. - Active participation in effective troubleshooting of equipment and processing issues - Ensuring all processing equipment and materials necessary are adequate and available to set the team up for success - Maintaining a high level of mechanical and technical aptitude and training - Ensuring all production activities are completed in a safe and compliant manor. - Joining a diverse shift team that will rely on consistent contributions to be successful   qualifications: - Prefer 4 year degree in biological/life science, but not required - HS Diploma or equivalent is required - Strongly desire background in science & technology, not just manufacturing   skills: 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. 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. Focusing on immune diseases like HIV that affect a large percentage of the population, the work our longtime partner conducts is imperative to a better, healthier future. To be recognized as a crucial part to furthering this goal, join this growing team 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: Rockville, Maryland job type: Contract salary: $20.40 - 24.00 per hour work hours: 9 to 5 education: Bachelors   responsibilities: - Being able to work a flexible shift schedule which includes coverage every other weekend. Includes possible placement on AM or PM shifts. - Completing daily manufacturing tasks per cGMPs, standard operating procedures, and batch document instructions - Monitoring critical process parameters - Documenting all manufacturing activities clearly and accurately. - Active participation in effective troubleshooting of equipment and processing issues - Ensuring all processing equipment and materials necessary are adequate and available to set the team up for success - Maintaining a high level of mechanical and technical aptitude and training - Ensuring all production activities are completed in a safe and compliant manor. - Joining a diverse shift team that will rely on consistent contributions to be successful   qualifications: - Prefer 4 year degree in biological/life science, but not required - HS Diploma or equivalent is required - Strongly desire background in science & technology, not just manufacturing   skills: 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. 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.
    • rockville, maryland
    • permanent
    • $110,000 - $120,000 per year
    job summary: Job Description: The Analytical Development Virologist is responsible for planning and executing assay transfer, development, qualification, and validation activities in the Analytical Development laboratory in support of biopharmaceuticals produced in the cGMP facility; proposes appropriate methods for GMP product characterization and release; provides analytical support to the Product Development group; identity, justify and implement laboratory instrumentation; ensure compliance with cGMPs and applicable regulatory guidelines for assay transfer and qualification/validation; assist with analytical method investigations; assist in project meetings to ensure that client requirements are met.   location: Rockville, Maryland job type: Permanent salary: $110,000 - 120,000 per year work hours: 9 to 5 education: Doctorate   responsibilities: Identify, develop, transfer and/or optimize and qualify/validate test methods for assigned projects.Perform analytical procedures, related testing, data review, trending, interpretation, and reporting of results. Assist with the resolution of deviations, OOS and CAPAs.Perform problem solving and troubleshooting; identify and resolve technical testing issues.Assist with expert technical guidance and communication to clients.Devise, implement and maintain analytical development programs to ensure the reliability of testing procedures, proper function of laboratory equipment, prepare and maintain applicable records.Prepare and review standard operation procedures, Test Methods, Qualification and Validation protocols, and reportsCreate and review technical documents including analytical development reports, data summaries, client presentations, etc.May be required to support other functions.Perform work in adherence to applicable regulatory guidelines such as ICH, USP, etc.Respond to client inquiries regarding services, develop proposals and manage projects and maintain appropriate records.Other duties as assigned  qualifications: Job Requirements Ph.D. degreeA minimum of 7 years of industry experience at the scientist level in analytical developmentMust be knowledgeable in virus methods. Must have experience in the development of PCR-based methods. Must be experienced with other non-cell-based virus analytical methods including SDS-PAGE, HPLC, Western blot, ELISA, etc. Experience in a GMP environmentDemonstrated ability to evaluate new technologies, new applications of existing technologies, and apply information and data from multiple scientific fields of study to create new solutions.Strong communicationTakes initiativeWorks well with all types of peopleRemains calm under pressure  skills: Analytical 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.EOEDisclaime 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: Job Description: The Analytical Development Virologist is responsible for planning and executing assay transfer, development, qualification, and validation activities in the Analytical Development laboratory in support of biopharmaceuticals produced in the cGMP facility; proposes appropriate methods for GMP product characterization and release; provides analytical support to the Product Development group; identity, justify and implement laboratory instrumentation; ensure compliance with cGMPs and applicable regulatory guidelines for assay transfer and qualification/validation; assist with analytical method investigations; assist in project meetings to ensure that client requirements are met.   location: Rockville, Maryland job type: Permanent salary: $110,000 - 120,000 per year work hours: 9 to 5 education: Doctorate   responsibilities: Identify, develop, transfer and/or optimize and qualify/validate test methods for assigned projects.Perform analytical procedures, related testing, data review, trending, interpretation, and reporting of results. Assist with the resolution of deviations, OOS and CAPAs.Perform problem solving and troubleshooting; identify and resolve technical testing issues.Assist with expert technical guidance and communication to clients.Devise, implement and maintain analytical development programs to ensure the reliability of testing procedures, proper function of laboratory equipment, prepare and maintain applicable records.Prepare and review standard operation procedures, Test Methods, Qualification and Validation protocols, and reportsCreate and review technical documents including analytical development reports, data summaries, client presentations, etc.May be required to support other functions.Perform work in adherence to applicable regulatory guidelines such as ICH, USP, etc.Respond to client inquiries regarding services, develop proposals and manage projects and maintain appropriate records.Other duties as assigned  qualifications: Job Requirements Ph.D. degreeA minimum of 7 years of industry experience at the scientist level in analytical developmentMust be knowledgeable in virus methods. Must have experience in the development of PCR-based methods. Must be experienced with other non-cell-based virus analytical methods including SDS-PAGE, HPLC, Western blot, ELISA, etc. Experience in a GMP environmentDemonstrated ability to evaluate new technologies, new applications of existing technologies, and apply information and data from multiple scientific fields of study to create new solutions.Strong communicationTakes initiativeWorks well with all types of peopleRemains calm under pressure  skills: Analytical 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.EOEDisclaime 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.
    • sterling, virginia
    • permanent
    • $43,500 - $54,000 per year
    Would you like to work for a company that is committed to their employees’ safety and where you will be recognized for your contributions? We are looking for Pharmacy Techs to join an innovative company in the Sterling, VA area. If you can ensure the safe and efficient work environment  we have the job for you!salary: $43,500 - $54,000 per yearshift: Thirdwork hours: 3 PM - 11 AMeducation: AssociateResponsibilitiesPerform the duties associated with compounding, dispensing, and distribution of FDG and NaF, including data entry with Pinestar for end-of-day reports and daily dose management reports.  Ensure compliance with USP,  proposed regulations, or other state pharmacy requirements as applicable, at the site level; maintain a personal license in good standing through applicable state laws.  Complete cGMP documents as required within SOFIE’s Quality Management System.  Ensure aseptic operations follow internal procedures (gowning, cleaning/sanitation, sterility, environmental monitoring, etc.), customer requirements, and FDA regulations.  Maintain a clean and safe working environment.The essential functions of this role include:manual lifting up to 50lbsSkillsTestingInventoryQuality ControlSanitationQualificationsYears of experience: 3 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.EOEDisclaime 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.
    Would you like to work for a company that is committed to their employees’ safety and where you will be recognized for your contributions? We are looking for Pharmacy Techs to join an innovative company in the Sterling, VA area. If you can ensure the safe and efficient work environment  we have the job for you!salary: $43,500 - $54,000 per yearshift: Thirdwork hours: 3 PM - 11 AMeducation: AssociateResponsibilitiesPerform the duties associated with compounding, dispensing, and distribution of FDG and NaF, including data entry with Pinestar for end-of-day reports and daily dose management reports.  Ensure compliance with USP,  proposed regulations, or other state pharmacy requirements as applicable, at the site level; maintain a personal license in good standing through applicable state laws.  Complete cGMP documents as required within SOFIE’s Quality Management System.  Ensure aseptic operations follow internal procedures (gowning, cleaning/sanitation, sterility, environmental monitoring, etc.), customer requirements, and FDA regulations.  Maintain a clean and safe working environment.The essential functions of this role include:manual lifting up to 50lbsSkillsTestingInventoryQuality ControlSanitationQualificationsYears of experience: 3 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.EOEDisclaime 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.
    • sterling, virginia
    • permanent
    • $24 - $30 per year
    Ready to let your ambition thrive? We are looking for a candidate with previous leadership experience within a fast-paced environment. In this role, you will be responsible for ensuring the production of quality control through production, operations, and manufacturing. This is a position with hands-on responsibility and accountability for daily production flow and bottom-line results.  salary: $24 - $30 per yearshift: Firstwork hours: 4 AM - 12 PMeducation: BachelorResponsibilitieso Ensure all materials/reagents are accepted according to SOPs and within expiry, o Ensure all equipment is appropriately qualified prior to use o Operate the synthesis unit according to SOPs o Learn the basic operational principles of the synthesis unit and assist in routine maintenance of the synthesis unit  Perform FDG and NaF quality control (QC) processes according to SOPs: o Assist with basic maintenance of QC equipment o Ensure all equipment is appropriately calibrated and qualified prior to using o Operate the QC equipment according to SOPs  Ensure completion of applicable cGMP documentation.  Assist with inventory managementThe essential functions of this role include:manual lifting up to 50lbsstanding for 4 hours at one timeSkillsProduction ControlQuality AssuranceQuality ControlCoachingProviding FeedbackOperationsTestingQualificationsYears of experience: 2 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.EOEDisclaime 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.
    Ready to let your ambition thrive? We are looking for a candidate with previous leadership experience within a fast-paced environment. In this role, you will be responsible for ensuring the production of quality control through production, operations, and manufacturing. This is a position with hands-on responsibility and accountability for daily production flow and bottom-line results.  salary: $24 - $30 per yearshift: Firstwork hours: 4 AM - 12 PMeducation: BachelorResponsibilitieso Ensure all materials/reagents are accepted according to SOPs and within expiry, o Ensure all equipment is appropriately qualified prior to use o Operate the synthesis unit according to SOPs o Learn the basic operational principles of the synthesis unit and assist in routine maintenance of the synthesis unit  Perform FDG and NaF quality control (QC) processes according to SOPs: o Assist with basic maintenance of QC equipment o Ensure all equipment is appropriately calibrated and qualified prior to using o Operate the QC equipment according to SOPs  Ensure completion of applicable cGMP documentation.  Assist with inventory managementThe essential functions of this role include:manual lifting up to 50lbsstanding for 4 hours at one timeSkillsProduction ControlQuality AssuranceQuality ControlCoachingProviding FeedbackOperationsTestingQualificationsYears of experience: 2 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.EOEDisclaime 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
    • $20.40 - $24 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. Focusing on immune diseases like HIV that affect a large percentage of the population, the work our longtime partner conducts is imperative to a better, healthier future. To be recognized as a crucial part to furthering this goal, join this growing team 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: Rockville, Maryland job type: Contract salary: $20.40 - 24.00 per hour work hours: 9 to 5 education: Bachelors   responsibilities: - Being able to work a flexible shift schedule which includes coverage every other weekend. Includes possible placement on AM or PM shifts. - Completing daily manufacturing tasks per cGMPs, standard operating procedures, and batch document instructions - Monitoring critical process parameters - Documenting all manufacturing activities clearly and accurately. - Active participation in effective troubleshooting of equipment and processing issues - Ensuring all processing equipment and materials necessary are adequate and available to set the team up for success - Maintaining a high level of mechanical and technical aptitude and training - Ensuring all production activities are completed in a safe and compliant manor. - Joining a diverse shift team that will rely on consistent contributions to be successful   qualifications: - Prefer 4 year degree in biological/life science, but not required - HS Diploma or equivalent is required - Strongly desire background in science & technology, not just manufacturing   skills: 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. 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. Focusing on immune diseases like HIV that affect a large percentage of the population, the work our longtime partner conducts is imperative to a better, healthier future. To be recognized as a crucial part to furthering this goal, join this growing team 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: Rockville, Maryland job type: Contract salary: $20.40 - 24.00 per hour work hours: 9 to 5 education: Bachelors   responsibilities: - Being able to work a flexible shift schedule which includes coverage every other weekend. Includes possible placement on AM or PM shifts. - Completing daily manufacturing tasks per cGMPs, standard operating procedures, and batch document instructions - Monitoring critical process parameters - Documenting all manufacturing activities clearly and accurately. - Active participation in effective troubleshooting of equipment and processing issues - Ensuring all processing equipment and materials necessary are adequate and available to set the team up for success - Maintaining a high level of mechanical and technical aptitude and training - Ensuring all production activities are completed in a safe and compliant manor. - Joining a diverse shift team that will rely on consistent contributions to be successful   qualifications: - Prefer 4 year degree in biological/life science, but not required - HS Diploma or equivalent is required - Strongly desire background in science & technology, not just manufacturing   skills: 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. 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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