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11 jobs found in berkeley, california

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    • san rafael, california
    • contract
    • $59.90 - $70.47 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. Internationally known for creating cutting-edge biopharmaceuticals for patients who live with rare genetic diseases, our partner strives to develop critical therapies for the small population - mostly children - that suffer from near unheard of conditions. If you're looking for an exciting opportunity to make a difference with an established company, this is the position 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: San Rafael, California job type: Contract salary: $59.90 - 70.47 per hour work hours: 8 to 4 education: Bachelors   responsibilities: Duties: For assigned study(ies), the Study Manager is accountable for day-to-day Clinical Operations study execution and related deliverables and is the primary point of contact within Clinical Operations for a study. Key responsibilities include: Managing risks, issues and opportunities that impact timeline, quality, and budget, overseeing the Clinical Operations study team, vendors and CRO, and collaborating with cross-functional representatives to execute on study deliverables.  qualifications: Skills: The candidate is expected to show and have proficiency and experience in the following competencies: Decision Making, Strategic Thinking, and Problem SolvingInfluence and Organizational AwarenessAgility and Proactivity Communication and Collaboration With advanced technical competencies in many of the following areas: Study Management and Execution Compliance and Quality Data Analysis and Interpretation Drug Development and Study Design Product and Therapeutic Area Knowledge Education: Minimum BA/BS7 years work experience in life sciences or medically related field, including 4 years of biopharmaceutical clinical research experience obtained working on clinical trials in a biotech, pharmaceutical or CROExperience in oversight of external vendors (e.g. CROs, central labs, imaging vendors, etc.)  skills: Clinical Study Design 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.Qualified applicants in San Francisco with criminal histories will be considered for employment in accordance with the San Francisco Fair Chance Ordinance. We will consider for employment all qualified Applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance. 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. Internationally known for creating cutting-edge biopharmaceuticals for patients who live with rare genetic diseases, our partner strives to develop critical therapies for the small population - mostly children - that suffer from near unheard of conditions. If you're looking for an exciting opportunity to make a difference with an established company, this is the position 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: San Rafael, California job type: Contract salary: $59.90 - 70.47 per hour work hours: 8 to 4 education: Bachelors   responsibilities: Duties: For assigned study(ies), the Study Manager is accountable for day-to-day Clinical Operations study execution and related deliverables and is the primary point of contact within Clinical Operations for a study. Key responsibilities include: Managing risks, issues and opportunities that impact timeline, quality, and budget, overseeing the Clinical Operations study team, vendors and CRO, and collaborating with cross-functional representatives to execute on study deliverables.  qualifications: Skills: The candidate is expected to show and have proficiency and experience in the following competencies: Decision Making, Strategic Thinking, and Problem SolvingInfluence and Organizational AwarenessAgility and Proactivity Communication and Collaboration With advanced technical competencies in many of the following areas: Study Management and Execution Compliance and Quality Data Analysis and Interpretation Drug Development and Study Design Product and Therapeutic Area Knowledge Education: Minimum BA/BS7 years work experience in life sciences or medically related field, including 4 years of biopharmaceutical clinical research experience obtained working on clinical trials in a biotech, pharmaceutical or CROExperience in oversight of external vendors (e.g. CROs, central labs, imaging vendors, etc.)  skills: Clinical Study Design 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.Qualified applicants in San Francisco with criminal histories will be considered for employment in accordance with the San Francisco Fair Chance Ordinance. We will consider for employment all qualified Applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance. 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.
    • berkeley, california
    • contract
    • $26.38 - $31.03 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. 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: Berkeley, California job type: Contract salary: $26.38 - 31.03 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Contract position is available to support QC Chemistry II group for release testing, method transfers to other equipment, equipment transfers from ESE to B88. Contractor will support testing, documentation, and general lab duties. Quality Control department, Chemistry group that performs testing on proteins. Testing is HPLC-based. Perform analytical testing to support the release, stability, and in process testing samples, or final products;Follow, accurately, relevant standard operating procedures (SOPs), perform all activities in accordance with certified good manufacturing practice (cGMP) requirements reports abnormalitiesInitiate and complete laboratory discrepancy events on timeKeep accurate documentation and track recordCompile, enter and review data into LIMS or other databases/Excel sheetsConfirm documents test results to ensure completeness and accuracy per cGMPs  qualifications: Required: Bachelor's degree in a scientific disciplineExperience with a cGMPExperience with chromatography systemsAbility to multi-task and good adaptabilityFocus on GoalsIntegrity and Commitment to Company Beliefs and Values Preferred: Experience with Wet-Chemical techniquesExperience with Chromatography  skills: Quality control, HPLC, SOP, MS-EXCEL, Chromatography, Protein Purification, GMP (Good Manufacturing Practice), LIMS (Laboratory Information Management System 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.Qualified applicants in San Francisco with criminal histories will be considered for employment in accordance with the San Francisco Fair Chance Ordinance. We will consider for employment all qualified Applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance. 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. 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: Berkeley, California job type: Contract salary: $26.38 - 31.03 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Contract position is available to support QC Chemistry II group for release testing, method transfers to other equipment, equipment transfers from ESE to B88. Contractor will support testing, documentation, and general lab duties. Quality Control department, Chemistry group that performs testing on proteins. Testing is HPLC-based. Perform analytical testing to support the release, stability, and in process testing samples, or final products;Follow, accurately, relevant standard operating procedures (SOPs), perform all activities in accordance with certified good manufacturing practice (cGMP) requirements reports abnormalitiesInitiate and complete laboratory discrepancy events on timeKeep accurate documentation and track recordCompile, enter and review data into LIMS or other databases/Excel sheetsConfirm documents test results to ensure completeness and accuracy per cGMPs  qualifications: Required: Bachelor's degree in a scientific disciplineExperience with a cGMPExperience with chromatography systemsAbility to multi-task and good adaptabilityFocus on GoalsIntegrity and Commitment to Company Beliefs and Values Preferred: Experience with Wet-Chemical techniquesExperience with Chromatography  skills: Quality control, HPLC, SOP, MS-EXCEL, Chromatography, Protein Purification, GMP (Good Manufacturing Practice), LIMS (Laboratory Information Management System 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.Qualified applicants in San Francisco with criminal histories will be considered for employment in accordance with the San Francisco Fair Chance Ordinance. We will consider for employment all qualified Applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance. 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.
    • san rafael, california
    • contract
    • $49.38 - $58.09 per hour
    job summary: We are seeking a highly motivated Technical Scientist / Scientist who can take a leadership role in moving forward the differentiation and characterization of gene-edited toxiC lines into high quality cardiomyocyte cultures. The successful candidate will be proficient with managing multiple projects and will have extensive iPS CM experience.   location: San Rafael, California job type: Contract salary: $49.38 - 58.09 per hour work hours: 9 to 5 education: Doctorate   responsibilities: For the Technical Scientist, the successful candidate will take on a leadership role, providing iPS CM differentiation services for several cardiovascular projects. For the Scientist, the successful candidate takes on a leadership role to conceive strategies, lead the development, evaluation, and implementation of state-of-the-art cell-based disease models to identify novel therapeutic interventions.This exploratory cell biology work will contribute to our understanding of the mechanisms of cardiac disease pathogenesis, and will also provide preclinical proof-of-concept data to guide in the development of novel and safe therapeutics for inherited cardiac diseases with unmet need.Perform cell biology work, publish findings in high-impact journals and present research at major conferences.Effectively partner with the program team, other scientists and the Research and Early Development leadership team to develop and execute on the program's strategic plan.Present program data at a range of internal forums, including Research Seminars and Leadership Team governance forums.Collaborate with various functions, CROs, university or analytical laboratories, business partners, as necessary to ensure appropriate/timely progression of projects.No direct reports associated with this position.  qualifications: A recent Ph.D. with strong experience in cardiovascular research and cardiovascular physiology, pharmacology or a related subject area is required. PhD or equivalent relevant experience plus 0-2+ years industry experience MS with 5+ yearsBS with 8+ years.Excellent working cell biology experience in at least one of the following: Functional cardiomyocyte assaysexperience with culturing iPS-derived cardiomyocytesisolation and maintenance of primary cardiac cellsmonitoring cardiac cell function with cardio xCELLigence or by high speed calcium imagingconfocal microscopyhigh content microscopylive cell imagingDNA editing Excellent written and verbal communication skillsStrong analytical skills. This role requires employees to be fully vaccinated against COVID-1   skills: Cell Biology, Immunoassays, 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.Qualified applicants in San Francisco with criminal histories will be considered for employment in accordance with the San Francisco Fair Chance Ordinance. We will consider for employment all qualified Applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance. 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: We are seeking a highly motivated Technical Scientist / Scientist who can take a leadership role in moving forward the differentiation and characterization of gene-edited toxiC lines into high quality cardiomyocyte cultures. The successful candidate will be proficient with managing multiple projects and will have extensive iPS CM experience.   location: San Rafael, California job type: Contract salary: $49.38 - 58.09 per hour work hours: 9 to 5 education: Doctorate   responsibilities: For the Technical Scientist, the successful candidate will take on a leadership role, providing iPS CM differentiation services for several cardiovascular projects. For the Scientist, the successful candidate takes on a leadership role to conceive strategies, lead the development, evaluation, and implementation of state-of-the-art cell-based disease models to identify novel therapeutic interventions.This exploratory cell biology work will contribute to our understanding of the mechanisms of cardiac disease pathogenesis, and will also provide preclinical proof-of-concept data to guide in the development of novel and safe therapeutics for inherited cardiac diseases with unmet need.Perform cell biology work, publish findings in high-impact journals and present research at major conferences.Effectively partner with the program team, other scientists and the Research and Early Development leadership team to develop and execute on the program's strategic plan.Present program data at a range of internal forums, including Research Seminars and Leadership Team governance forums.Collaborate with various functions, CROs, university or analytical laboratories, business partners, as necessary to ensure appropriate/timely progression of projects.No direct reports associated with this position.  qualifications: A recent Ph.D. with strong experience in cardiovascular research and cardiovascular physiology, pharmacology or a related subject area is required. PhD or equivalent relevant experience plus 0-2+ years industry experience MS with 5+ yearsBS with 8+ years.Excellent working cell biology experience in at least one of the following: Functional cardiomyocyte assaysexperience with culturing iPS-derived cardiomyocytesisolation and maintenance of primary cardiac cellsmonitoring cardiac cell function with cardio xCELLigence or by high speed calcium imagingconfocal microscopyhigh content microscopylive cell imagingDNA editing Excellent written and verbal communication skillsStrong analytical skills. This role requires employees to be fully vaccinated against COVID-1   skills: Cell Biology, Immunoassays, 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.Qualified applicants in San Francisco with criminal histories will be considered for employment in accordance with the San Francisco Fair Chance Ordinance. We will consider for employment all qualified Applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance. 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.
    • san mateo, california
    • permanent
    • $110,000 - $135,000 per year
    job summary: The Clinical Lab Scientist (CLS) will be responsible for the day-to-day operations of the lab. CLSs will be working closely with Clinical Lab Assistants (CLAs) and Supervisor to make sure production goals (e.g., Timeliness and Accuracy of Analysis Report) are met. This role is fundamental to our patient service delivery and plays an integral role in providing a best-in-class patient experience. The CLS will ensure that all case samples are processed and accounted for daily.   location: San Mateo, California job type: Permanent salary: $110,000 - 135,000 per year work hours: 9 to 5 education: Bachelors   responsibilities: Perform accurate testing while maintaining departmental expectations.Follows GLP (Good Laboratory Practice); reports any non-conformity of SOPs to SupervisorEnsures tests are being completed according to approved proceduresAssist the Supervisor in completing projects assignedTrain new hires with the current lab processes and procedures and assists the Supervisor in SOP implementation.Assist the Supervisor in completing staff's competency testingEscalate, classify, and prioritize results issues to SupervisorMaintain best in class client experience standards for the companyShould understand the entire lab process and basic troubleshooting when errors occur.  qualifications: Bachelor's (BA / BS) degree or equivalent in Biological Sciences or related fieldCurrent ASCP board certification in Medical Laboratory Science and California State License for Clinical Laboratory Scientist (CLS) provided by CDPH1 to 3 years of experience in a CLIA lab environment preferredExtremely strong organizational skills and attention to detail.Excellent written and verbal communication skillsA proven track record of issue spotting and escalating issues as necessaryDemonstrated track record of successes in getting things on time  skills: Cell Biology, Biology, GLP (Good Laboratory Practice), Sample Preparation, Sample Testing 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: The Clinical Lab Scientist (CLS) will be responsible for the day-to-day operations of the lab. CLSs will be working closely with Clinical Lab Assistants (CLAs) and Supervisor to make sure production goals (e.g., Timeliness and Accuracy of Analysis Report) are met. This role is fundamental to our patient service delivery and plays an integral role in providing a best-in-class patient experience. The CLS will ensure that all case samples are processed and accounted for daily.   location: San Mateo, California job type: Permanent salary: $110,000 - 135,000 per year work hours: 9 to 5 education: Bachelors   responsibilities: Perform accurate testing while maintaining departmental expectations.Follows GLP (Good Laboratory Practice); reports any non-conformity of SOPs to SupervisorEnsures tests are being completed according to approved proceduresAssist the Supervisor in completing projects assignedTrain new hires with the current lab processes and procedures and assists the Supervisor in SOP implementation.Assist the Supervisor in completing staff's competency testingEscalate, classify, and prioritize results issues to SupervisorMaintain best in class client experience standards for the companyShould understand the entire lab process and basic troubleshooting when errors occur.  qualifications: Bachelor's (BA / BS) degree or equivalent in Biological Sciences or related fieldCurrent ASCP board certification in Medical Laboratory Science and California State License for Clinical Laboratory Scientist (CLS) provided by CDPH1 to 3 years of experience in a CLIA lab environment preferredExtremely strong organizational skills and attention to detail.Excellent written and verbal communication skillsA proven track record of issue spotting and escalating issues as necessaryDemonstrated track record of successes in getting things on time  skills: Cell Biology, Biology, GLP (Good Laboratory Practice), Sample Preparation, Sample Testing 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.
    • san mateo, california
    • permanent
    • $55,000 - $75,000 per year
    job summary: The Clinical Lab Assistant (CLA) will be responsible for assisting in the day-to-day operations of the lab (i.e. Accessioning, Preparation and Analysis of Samples). CLAs will be working closely with Clinical Lab Scientists and Supervisor to make sure production goals (e.g., Accuracy of Analysis Report) are met. This role is fundamental to our patient service delivery and plays an integral role in providing a best-in-class patient experience. Daily, the CLA will verify the proper specimen being analyzed for patients and perform the correct tests that need to be completed. Additionally, the CLA should understand the entire lab process and identify issues when they arise.   location: San Mateo, California job type: Permanent salary: $55,000 - 75,000 per year work hours: 9 to 5 education: Bachelors   responsibilities: Assists the team in day-to-day lab operations according to standard operating proceduresFollows GLP (Good Laboratory Practice); reports any non-conformity of SOPs to SupervisorEnsures production work is consistently completed in a timely manner and accounted forEscalate, classify, and prioritize results issues to SupervisorMaintain best in class client experience standards  qualifications: Bachelor's (BA / BS) degree or equivalent in Biological Sciences or related field1 to 3 years of experience in a CLIA lab environment preferredExtremely strong organizational skills and attention to detail.Excellent written and verbal communication skillsA proven track record of issue spotting and escalating issues as necessaryDemonstrated track record of successes in getting things on time  skills: Cell Biology, Biology, GLP (Good Laboratory Practice), Microbiology, Sample Preparation, Sample Testing 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: The Clinical Lab Assistant (CLA) will be responsible for assisting in the day-to-day operations of the lab (i.e. Accessioning, Preparation and Analysis of Samples). CLAs will be working closely with Clinical Lab Scientists and Supervisor to make sure production goals (e.g., Accuracy of Analysis Report) are met. This role is fundamental to our patient service delivery and plays an integral role in providing a best-in-class patient experience. Daily, the CLA will verify the proper specimen being analyzed for patients and perform the correct tests that need to be completed. Additionally, the CLA should understand the entire lab process and identify issues when they arise.   location: San Mateo, California job type: Permanent salary: $55,000 - 75,000 per year work hours: 9 to 5 education: Bachelors   responsibilities: Assists the team in day-to-day lab operations according to standard operating proceduresFollows GLP (Good Laboratory Practice); reports any non-conformity of SOPs to SupervisorEnsures production work is consistently completed in a timely manner and accounted forEscalate, classify, and prioritize results issues to SupervisorMaintain best in class client experience standards  qualifications: Bachelor's (BA / BS) degree or equivalent in Biological Sciences or related field1 to 3 years of experience in a CLIA lab environment preferredExtremely strong organizational skills and attention to detail.Excellent written and verbal communication skillsA proven track record of issue spotting and escalating issues as necessaryDemonstrated track record of successes in getting things on time  skills: Cell Biology, Biology, GLP (Good Laboratory Practice), Microbiology, Sample Preparation, Sample Testing 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.
    • berkeley, california
    • contract
    • $43.59 - $51.28 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. 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, subject to a valid medical or religious accommodation.   location: Berkeley, California job type: Contract salary: $43.59 - 51.28 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Support Technical Training and Site Compliance in an effective and efficient manner for Berkeley Site. Ensure compliant and timely support for web-based and other learning methodologies and ensuring all training records and documentation are current through establishment of training metrics, and monitoring training effectiveness. Promote knowledge sharing and use of e-Learning tools for technical training and qualification documentation to drive compliant solutions and reduce inefficiencies. Support the On the Job Training Record paperless project and validation work; including data entry and scanning processes.Accountable for the accuracy and integrity of all hard copy training records and training databases.Manage LMS and hard copy training records programs to ensure on-going compliance to training policies and procedures. Where compliance gaps are found, take immediate steps to correct and maintain compliance.Track and implement content/item changes and LMS reporting. Maintain revision control of training content and materials regardless of media and delivery method.Create Web Based and live learning content using a variety of authoring and editing tools, including Lectora, Snap!, Camtasia, Photoshop, Premiere Pro, Soundbooth, Snagit, and other related multimedia tools.Work with Technical Training Managers to ensure that web-based and live courses are kept up to date and are in line with best practices. Stay up to date with relevant systems, software and online training technology. Own and maintain equipment and software used for training purposes and manage upgrades when necessary. Support Technical Training and Site Compliance in an effective and efficient manner for Berkeley Site. Ensure compliant and timely support for web-based and other learning methodologies and ensuring all training records and documentation are current through establishment of training metrics, and monitoring training effectiveness. Promote knowledge sharing and use of e-Learning tools for technical training and qualification documentation to drive compliant solutions and reduce inefficiencies.Create and manage online training Items and Content Objects in a Learning Management System (preferable Plateau). Participate in the company user community to assist in the design, development, and testing of instructional materials. Beta-test new courses offered through myLearning. Seek electronic methods of documenting paperless training.Ensure revision control of all compliance-based electronic and hard-copy course materials and SOP's to include e-learning courseware.Deliver training to address the root cause of training-related department wide CAPAs and assist with delivery of site-wide courses for discrepancy investigators.Manage training participant course interactions (registration, troubleshooting, course questions, etc.). Coordinates all training resources (materials, scheduling, rooms, catering, and facilitators). Creates implements and evaluates tools to measure the effectiveness of training (e.g. proficiency checklists, assessments)  qualifications: Qualification BS or higher education preferredMinimum 4 to 6 years of relevant experience with emphasis on training coordination and delivery.Experience in training in a production environment is desirable or an equivalent combination of education and experience.Strong organizational and project management capabilities Interpersonal skills-strong teamwork, foster peer relationships, find common ground and solve problems with peersStrong communication skills and influencing skillsExercises independent thinking and problem solvingExcellent written and oral communication skills and experience presenting to diverse audiencesKnowledge of LMS administration, maintenance, reporting functionality (Success Factors/Plateau preferred) Advanced understanding of unique program and content requirements for eLearning and Learning Management Systems (LMS)Demonstrated project management skills, attention to details, ability to work independently in a lead role, to work on multiple projects and manage competing deadlinesExperienced with enterprise-wide learning management systems, e-learning programs, and structured training methods and processesComputer proficient with word processing, excel, graphics program and databasesFocus is internal and external. Interacts with subordinates, peers and Department Heads.Maintains an external network in field of expertise.Demonstrates integrity and firm commitment to company beliefs and values.Key Working Relationship Focus is internal and external. Interacts with subordinates, peers and Department Heads. Maintains an external network in field of expertise. Demonstrates integrity and firm commitment to company beliefs and values.  skills: Quality control, SOP, LIMS (Laboratory Information Management System 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.Qualified applicants in San Francisco with criminal histories will be considered for employment in accordance with the San Francisco Fair Chance Ordinance. We will consider for employment all qualified Applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance. 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. 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, subject to a valid medical or religious accommodation.   location: Berkeley, California job type: Contract salary: $43.59 - 51.28 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Support Technical Training and Site Compliance in an effective and efficient manner for Berkeley Site. Ensure compliant and timely support for web-based and other learning methodologies and ensuring all training records and documentation are current through establishment of training metrics, and monitoring training effectiveness. Promote knowledge sharing and use of e-Learning tools for technical training and qualification documentation to drive compliant solutions and reduce inefficiencies. Support the On the Job Training Record paperless project and validation work; including data entry and scanning processes.Accountable for the accuracy and integrity of all hard copy training records and training databases.Manage LMS and hard copy training records programs to ensure on-going compliance to training policies and procedures. Where compliance gaps are found, take immediate steps to correct and maintain compliance.Track and implement content/item changes and LMS reporting. Maintain revision control of training content and materials regardless of media and delivery method.Create Web Based and live learning content using a variety of authoring and editing tools, including Lectora, Snap!, Camtasia, Photoshop, Premiere Pro, Soundbooth, Snagit, and other related multimedia tools.Work with Technical Training Managers to ensure that web-based and live courses are kept up to date and are in line with best practices. Stay up to date with relevant systems, software and online training technology. Own and maintain equipment and software used for training purposes and manage upgrades when necessary. Support Technical Training and Site Compliance in an effective and efficient manner for Berkeley Site. Ensure compliant and timely support for web-based and other learning methodologies and ensuring all training records and documentation are current through establishment of training metrics, and monitoring training effectiveness. Promote knowledge sharing and use of e-Learning tools for technical training and qualification documentation to drive compliant solutions and reduce inefficiencies.Create and manage online training Items and Content Objects in a Learning Management System (preferable Plateau). Participate in the company user community to assist in the design, development, and testing of instructional materials. Beta-test new courses offered through myLearning. Seek electronic methods of documenting paperless training.Ensure revision control of all compliance-based electronic and hard-copy course materials and SOP's to include e-learning courseware.Deliver training to address the root cause of training-related department wide CAPAs and assist with delivery of site-wide courses for discrepancy investigators.Manage training participant course interactions (registration, troubleshooting, course questions, etc.). Coordinates all training resources (materials, scheduling, rooms, catering, and facilitators). Creates implements and evaluates tools to measure the effectiveness of training (e.g. proficiency checklists, assessments)  qualifications: Qualification BS or higher education preferredMinimum 4 to 6 years of relevant experience with emphasis on training coordination and delivery.Experience in training in a production environment is desirable or an equivalent combination of education and experience.Strong organizational and project management capabilities Interpersonal skills-strong teamwork, foster peer relationships, find common ground and solve problems with peersStrong communication skills and influencing skillsExercises independent thinking and problem solvingExcellent written and oral communication skills and experience presenting to diverse audiencesKnowledge of LMS administration, maintenance, reporting functionality (Success Factors/Plateau preferred) Advanced understanding of unique program and content requirements for eLearning and Learning Management Systems (LMS)Demonstrated project management skills, attention to details, ability to work independently in a lead role, to work on multiple projects and manage competing deadlinesExperienced with enterprise-wide learning management systems, e-learning programs, and structured training methods and processesComputer proficient with word processing, excel, graphics program and databasesFocus is internal and external. Interacts with subordinates, peers and Department Heads.Maintains an external network in field of expertise.Demonstrates integrity and firm commitment to company beliefs and values.Key Working Relationship Focus is internal and external. Interacts with subordinates, peers and Department Heads. Maintains an external network in field of expertise. Demonstrates integrity and firm commitment to company beliefs and values.  skills: Quality control, SOP, LIMS (Laboratory Information Management System 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.Qualified applicants in San Francisco with criminal histories will be considered for employment in accordance with the San Francisco Fair Chance Ordinance. We will consider for employment all qualified Applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance. 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 san francisco, california
    • contract
    • $35 - $41.77 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. Position Type: Long-term contract position for 1 year with potential for full time hire.   location: South San Francisco, California job type: Contract salary: $35.00 - 41.77 per hour work hours: 8 to 4 education: Bachelors   responsibilities: Contract position for one year. This position will primarily support the pathology team by performing immunohistochemistry and other laboratory-based deliverables. The Ideal candidate will have practical and educational laboratory experience performing immunohistochemistry on a variety of automated platforms such as, DAKO Link48 and Omnis, Lecia BOND Rx and Ventana platforms. Previous industry experience working in a research pathology, histology lab, or clinical anatomical pathology lab is desired.Ability to independently perform established immunohistochemistry protocols and procedures on laboratory automationScanning of slides on Aperio scanners and QC of imagesRecording experiment details into electronic laboratory notebookAssist with pathology sample operations and logistics such as organizing, coordinating, packaging and shipping samples. Lifting requirement of 25 lbsDaily and weekly maintenance of laboratory equipmentWeekly maintenance of laboratory reagent inventories and stocks  qualifications: Experience with independently performing immunohistochemistry protocolsExperience with multiple slide staining platformsAble to work independently within a team settingHigh attention to detailStrong verbal and written communication skillsStrong organizational skillsComfortable with shifting prioritiesFlexible and adaptable thinkingCollaborative, positive,MS Office skillsStrong preference given to candidates with industry pathology and histology experience  skills: MS-EXCEL, GLP (Good Laboratory 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.Qualified applicants in San Francisco with criminal histories will be considered for employment in accordance with the San Francisco Fair Chance Ordinance. We will consider for employment all qualified Applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance. 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. Position Type: Long-term contract position for 1 year with potential for full time hire.   location: South San Francisco, California job type: Contract salary: $35.00 - 41.77 per hour work hours: 8 to 4 education: Bachelors   responsibilities: Contract position for one year. This position will primarily support the pathology team by performing immunohistochemistry and other laboratory-based deliverables. The Ideal candidate will have practical and educational laboratory experience performing immunohistochemistry on a variety of automated platforms such as, DAKO Link48 and Omnis, Lecia BOND Rx and Ventana platforms. Previous industry experience working in a research pathology, histology lab, or clinical anatomical pathology lab is desired.Ability to independently perform established immunohistochemistry protocols and procedures on laboratory automationScanning of slides on Aperio scanners and QC of imagesRecording experiment details into electronic laboratory notebookAssist with pathology sample operations and logistics such as organizing, coordinating, packaging and shipping samples. Lifting requirement of 25 lbsDaily and weekly maintenance of laboratory equipmentWeekly maintenance of laboratory reagent inventories and stocks  qualifications: Experience with independently performing immunohistochemistry protocolsExperience with multiple slide staining platformsAble to work independently within a team settingHigh attention to detailStrong verbal and written communication skillsStrong organizational skillsComfortable with shifting prioritiesFlexible and adaptable thinkingCollaborative, positive,MS Office skillsStrong preference given to candidates with industry pathology and histology experience  skills: MS-EXCEL, GLP (Good Laboratory 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.Qualified applicants in San Francisco with criminal histories will be considered for employment in accordance with the San Francisco Fair Chance Ordinance. We will consider for employment all qualified Applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance. 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.
    • san rafael, california
    • contract
    • $34.23 - $40.27 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. Internationally known for creating cutting-edge biopharmaceuticals for patients who live with rare genetic diseases, our partner strives to develop critical therapies for the small population - mostly children - that suffer from near unheard of conditions. If you're looking for an exciting opportunity to make a difference with an established company, this is the position for you! This role requires employees to be fully vaccinated against COVID-19 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: San Rafael, California job type: Contract salary: $34.23 - 40.27 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Description: BioAnalytical Sciences develops analytical methods for detection of drug, antibodies to protein therapeutics, and biomarkers in biological matrices from non-clinical and clinical subjects to support projects through multiple stages of development. The qualified candidate plans and performs activities required for Critical Reagent preparation, characterization, and release testing in a regulated environment while exercising significant technical discretion. Responsibilities can include sample preparation, sample analysis, GLP documentation, report and SOP generation, assay validation and troubleshooting. Produce consistently prepared and well characterized reagents to reduce the risk of assay failure and ensure methods meet regulatory requirements.Responsible for the development and quality of Critical Reagents including purifying proteins, conducting protein conjugations (e.g. biotinylation, ruthenylation using standard chemistry), purifying DNA plasmids, assessing their purity, affinity, and concentration, and generating Certificates of Analysis.Monitors and or trend lot-to-lot variability, and may assist with reagent troubleshootingEnhance the analytical capabilities of the group.Prepare SOPs, reports and documents such as characterization protocols, development reports, and testing data reports.Share responsibility for lab maintenance duties.Participates in meetings and presents data.Responsible for the generation, characterization, and release of critical reagents used in clinical and non-clinical sample analysis, the CRG Research Associate will be a critical service to the assay development and testing groups by building and continuously supplying customized protein reagents for internal and outsourced assays.  qualifications: Required Skills: Bachelor's degree and at least 4 years of experience in a bioanalytical laboratory, research laboratory, or biotechnology company. Master's degree with at least 2 years of relevant experience. Preferred Skills: Skills with protein conjugations, protein characterization (including SDS-PAGE, Western Blot, HPLC), chromatography systems (experience with Akta instruments preferred), DNA plasmid purification and characterization, and other analytical methods or analytical experience in a regulated lab environmentExperience with generating Standard Operating Procedures and Protocols.Excellent writing and verbal communications skills.Analyzes data and summarizes results independently, then proposes interpretations and next steps in consultation with supervisor The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is occasionally exposed to work near moving mechanical parts; fumes or airborne particles; toxic or caustic chemicals; risk of electrical shock and vibration. The noise level in the work environment is usually moderate. The employee may frequently be required to sit and talk or hear. The employee is occasionally required to stand; walk; use hands to finger, handle, or feel; reach with hands and arms; climb or balance; stoop, kneel, crouch, or crawl and taste or smell. The employee must occasionally lift and/or move up to 25 pounds. Specific vision abilities by this job include close vision, depth perception and ability to adjust focus.   skills: SOP, GLP (Good Laboratory 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.Qualified applicants in San Francisco with criminal histories will be considered for employment in accordance with the San Francisco Fair Chance Ordinance. We will consider for employment all qualified Applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance. 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. Internationally known for creating cutting-edge biopharmaceuticals for patients who live with rare genetic diseases, our partner strives to develop critical therapies for the small population - mostly children - that suffer from near unheard of conditions. If you're looking for an exciting opportunity to make a difference with an established company, this is the position for you! This role requires employees to be fully vaccinated against COVID-19 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: San Rafael, California job type: Contract salary: $34.23 - 40.27 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Description: BioAnalytical Sciences develops analytical methods for detection of drug, antibodies to protein therapeutics, and biomarkers in biological matrices from non-clinical and clinical subjects to support projects through multiple stages of development. The qualified candidate plans and performs activities required for Critical Reagent preparation, characterization, and release testing in a regulated environment while exercising significant technical discretion. Responsibilities can include sample preparation, sample analysis, GLP documentation, report and SOP generation, assay validation and troubleshooting. Produce consistently prepared and well characterized reagents to reduce the risk of assay failure and ensure methods meet regulatory requirements.Responsible for the development and quality of Critical Reagents including purifying proteins, conducting protein conjugations (e.g. biotinylation, ruthenylation using standard chemistry), purifying DNA plasmids, assessing their purity, affinity, and concentration, and generating Certificates of Analysis.Monitors and or trend lot-to-lot variability, and may assist with reagent troubleshootingEnhance the analytical capabilities of the group.Prepare SOPs, reports and documents such as characterization protocols, development reports, and testing data reports.Share responsibility for lab maintenance duties.Participates in meetings and presents data.Responsible for the generation, characterization, and release of critical reagents used in clinical and non-clinical sample analysis, the CRG Research Associate will be a critical service to the assay development and testing groups by building and continuously supplying customized protein reagents for internal and outsourced assays.  qualifications: Required Skills: Bachelor's degree and at least 4 years of experience in a bioanalytical laboratory, research laboratory, or biotechnology company. Master's degree with at least 2 years of relevant experience. Preferred Skills: Skills with protein conjugations, protein characterization (including SDS-PAGE, Western Blot, HPLC), chromatography systems (experience with Akta instruments preferred), DNA plasmid purification and characterization, and other analytical methods or analytical experience in a regulated lab environmentExperience with generating Standard Operating Procedures and Protocols.Excellent writing and verbal communications skills.Analyzes data and summarizes results independently, then proposes interpretations and next steps in consultation with supervisor The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is occasionally exposed to work near moving mechanical parts; fumes or airborne particles; toxic or caustic chemicals; risk of electrical shock and vibration. The noise level in the work environment is usually moderate. The employee may frequently be required to sit and talk or hear. The employee is occasionally required to stand; walk; use hands to finger, handle, or feel; reach with hands and arms; climb or balance; stoop, kneel, crouch, or crawl and taste or smell. The employee must occasionally lift and/or move up to 25 pounds. Specific vision abilities by this job include close vision, depth perception and ability to adjust focus.   skills: SOP, GLP (Good Laboratory 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.Qualified applicants in San Francisco with criminal histories will be considered for employment in accordance with the San Francisco Fair Chance Ordinance. We will consider for employment all qualified Applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance. 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.
    • san rafael, california
    • contract
    • $51.35 - $60.41 per hour
    job summary: Looking for a self-motivated team player with a minimum of 4 years laboratory experience. The successful candidate will support Research & Development in generating viral and non-viral gene therapy for rare genetic diseases, and to understand drug response variabilities. The Senior Research Associate will work closely with a team of dedicated researchers, and be committed to working in the bench, handling pre-clinical/clinical trial samples, and computational analysis. 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: San Rafael, California job type: Contract salary: $51.35 - 60.41 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Careful handling and processing of tissues for high throughput sequencing, and proteomics analysis.Execution of validated molecular biology assays including nucleic acid isolation (DNA and RNA), library preparation, and QC validations.Develop and use varied molecular biology and analytical assays including, Real-time PCR, droplet digital PCR, Enzyme activity assays, ELISA, western blotting, etc.Develop and validate new molecular assays for therapeutic development.Analysis of high throughput sequencing and proteomics data.The successful candidate is expected to be independent, collaborative, and promote a collegial workplace.  qualifications: Bachelor's degree (BS) and at least 6 years of experience, OR Master's degree (MS) with at least 4 years of relevant experience.Having an Industry experience is a plus for consideration.Prior hands-on experience handling biological/clinical samples.Basic molecular biology (PCR, RT-PCR, western blot), and mammalian cell culture techniques.Independently establishes new techniques, technologies, or methods based on evolving project demands.Experience using computational tools for sequence and protein analysis.Exceptional communication and organization skills.Ability to effectively multitask and have a strong desire to learn and contribute.Willingness to accept new responsibilities.Able to integrate and assist within varying cross-functional teams.  skills: Molecular Biology, PCR, GLP (Good Laboratory Practice), Cell Cultures, RT-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.Qualified applicants in San Francisco with criminal histories will be considered for employment in accordance with the San Francisco Fair Chance Ordinance. We will consider for employment all qualified Applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance. 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: Looking for a self-motivated team player with a minimum of 4 years laboratory experience. The successful candidate will support Research & Development in generating viral and non-viral gene therapy for rare genetic diseases, and to understand drug response variabilities. The Senior Research Associate will work closely with a team of dedicated researchers, and be committed to working in the bench, handling pre-clinical/clinical trial samples, and computational analysis. 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: San Rafael, California job type: Contract salary: $51.35 - 60.41 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Careful handling and processing of tissues for high throughput sequencing, and proteomics analysis.Execution of validated molecular biology assays including nucleic acid isolation (DNA and RNA), library preparation, and QC validations.Develop and use varied molecular biology and analytical assays including, Real-time PCR, droplet digital PCR, Enzyme activity assays, ELISA, western blotting, etc.Develop and validate new molecular assays for therapeutic development.Analysis of high throughput sequencing and proteomics data.The successful candidate is expected to be independent, collaborative, and promote a collegial workplace.  qualifications: Bachelor's degree (BS) and at least 6 years of experience, OR Master's degree (MS) with at least 4 years of relevant experience.Having an Industry experience is a plus for consideration.Prior hands-on experience handling biological/clinical samples.Basic molecular biology (PCR, RT-PCR, western blot), and mammalian cell culture techniques.Independently establishes new techniques, technologies, or methods based on evolving project demands.Experience using computational tools for sequence and protein analysis.Exceptional communication and organization skills.Ability to effectively multitask and have a strong desire to learn and contribute.Willingness to accept new responsibilities.Able to integrate and assist within varying cross-functional teams.  skills: Molecular Biology, PCR, GLP (Good Laboratory Practice), Cell Cultures, RT-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.Qualified applicants in San Francisco with criminal histories will be considered for employment in accordance with the San Francisco Fair Chance Ordinance. We will consider for employment all qualified Applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance. 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.
    • san rafael, california
    • contract
    • $47.92 - $56.38 per hour
    job summary: The mission of the Biology Research department is to conduct preclinical research evaluating potential therapeutics for severe rare diseases with unmet medical needs. Our team in the non-oncology hematology group uses state-of-the art equipment to provide biochemical and molecular biology support to a variety of pre-clinical projects. We are searching for a self-motivated Technical Scientist with 4-8 years of hands-on laboratory experience. The successful candidate will develop and use biochemical assays to measure pharmacodynamics, pharmacokinetics, immunogenicity and biomarkers of new therapeutics. The Technical Scientist will work closely with a team of dedicated researchers and will have the opportunity positively impact the lives of patients with rare diseases.   location: San Rafael, California job type: Contract salary: $47.92 - 56.38 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Develop and use a variety of analytical methods to detect biomarkers, drug, and antibodies in biological matrices. Techniques may include (but are not limited to) ELISA, enzyme activity assays, DNA / RNA extraction and droplet digital polymerase chain reaction (ddPCR).Develop new techniques, or bring in new technology from the outside, to enhance the analytical capabilities of the group.Present results, conclusions, and implications to project teams.Meticulously adhere to electronic data recording standards.Share responsibility for lab management duties.Contribute to reports and peer-reviewed publications.This role is primarily based at the bench / in the lab.  qualifications: Bachelor's degree (BS) and at least 10 years of experienceMaster's degree (MS) with at least 8 years of relevant experience8-10 years of laboratory experience, or demonstrated experience as an independent researcher.Broad technical proficiency and ability to solve complex scientific and technical issues independently.Experience with handling animal tissues is desired.Excellent verbal and written communication skills: ability to prepare and present data in group settings, prepare formal reports, communicate across functions.The position requires organizational skills, self-motivation, teamwork, and dedication to quality in a fast-paced setting. Hands-on experience performing molecular biology, immunoassays, or other analytical methods in a biological or biochemical field.Working knowledge of cell and molecular biology and biochemistry. This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   skills: Molecular Biology, Cell Biology, PCR, Immunoassays 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.Qualified applicants in San Francisco with criminal histories will be considered for employment in accordance with the San Francisco Fair Chance Ordinance. We will consider for employment all qualified Applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance. 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 mission of the Biology Research department is to conduct preclinical research evaluating potential therapeutics for severe rare diseases with unmet medical needs. Our team in the non-oncology hematology group uses state-of-the art equipment to provide biochemical and molecular biology support to a variety of pre-clinical projects. We are searching for a self-motivated Technical Scientist with 4-8 years of hands-on laboratory experience. The successful candidate will develop and use biochemical assays to measure pharmacodynamics, pharmacokinetics, immunogenicity and biomarkers of new therapeutics. The Technical Scientist will work closely with a team of dedicated researchers and will have the opportunity positively impact the lives of patients with rare diseases.   location: San Rafael, California job type: Contract salary: $47.92 - 56.38 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Develop and use a variety of analytical methods to detect biomarkers, drug, and antibodies in biological matrices. Techniques may include (but are not limited to) ELISA, enzyme activity assays, DNA / RNA extraction and droplet digital polymerase chain reaction (ddPCR).Develop new techniques, or bring in new technology from the outside, to enhance the analytical capabilities of the group.Present results, conclusions, and implications to project teams.Meticulously adhere to electronic data recording standards.Share responsibility for lab management duties.Contribute to reports and peer-reviewed publications.This role is primarily based at the bench / in the lab.  qualifications: Bachelor's degree (BS) and at least 10 years of experienceMaster's degree (MS) with at least 8 years of relevant experience8-10 years of laboratory experience, or demonstrated experience as an independent researcher.Broad technical proficiency and ability to solve complex scientific and technical issues independently.Experience with handling animal tissues is desired.Excellent verbal and written communication skills: ability to prepare and present data in group settings, prepare formal reports, communicate across functions.The position requires organizational skills, self-motivation, teamwork, and dedication to quality in a fast-paced setting. Hands-on experience performing molecular biology, immunoassays, or other analytical methods in a biological or biochemical field.Working knowledge of cell and molecular biology and biochemistry. This role requires employees to be fully vaccinated against COVID-19 as a condition of employment, subject to a valid medical or religious accommodation.   skills: Molecular Biology, Cell Biology, PCR, Immunoassays 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.Qualified applicants in San Francisco with criminal histories will be considered for employment in accordance with the San Francisco Fair Chance Ordinance. We will consider for employment all qualified Applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance. 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.
    • san rafael, california
    • contract
    • $42.79 - $50.34 per hour
    job summary: The Research & Development (R&D) group is responsible for everything from research and discovery to post-market clinical development. Research & Development (R&D) involves all bench and clinical research and the associated groups that support those endeavors. Our teams work on developing first-in-class and best-in-class therapeutics that provide meaningful advances to patients who live with rare diseases. Come join our team and make a meaningful impact on patients' lives. We are looking for a highly motivated team member with extensive experience in mammalian cell culture models to be a key contributor to the Research Gene Therapy Group. The incumbent will be responsible for supporting the development of primary, iPSC-derived, and immortalized cell-based models for expression, safety, and functional testing of gene therapy candidates. The incumbent will also execute routine molecular and biochemical analyses and utilize novel state of the art technologies like next generation sequencing. 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: San Rafael, California job type: Contract salary: $42.79 - 50.34 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Perform routine cell culture as well as viral (AAV / LV) and non-viral modification of adherent, suspension, iPSC-derived and primary cell linesDesign, modify, and clone DNA constructs for expression of proteins and fusion proteins in mammalian expression systemsPerform standard molecular biology techniques including DNA extraction, RNA extraction, and PCR / ddPCRApply basic biochemical and immunological techniques, including protein extraction, protein gel electrophoresis, conventional and capillary western blotting, ELISA, and flow cytometryPerform routine molecular biology techniques using the engineered cell lines to support development of new next-generation sequencing (NGS) assays for sequence determination, editing efficiency analysis, and off-target assessmentMaintain detailed records of experimental protocols and data in electronic laboratory notebook in accordance with company policyEffectively collaborate with a fully integrated research team to facilitate the success of projects  qualifications: Bachelor's (BS) degree or Master's (MS) in Molecular Biology, Biochemistry, Synthetic Biology or relevant biological sciencesGene therapy or gene editing experience preferred, including working knowledge of state-of-the-art technologies utilized in the field.Strong technical background with standard laboratory methods, including culturing immortalized, iPSC-derived and primary cells; molecular biology and cloning; (q)PCR; ELISA; intracellular staining; western blotting; DNA transfection and viral transduction; flow cytometry or microscopyAbility to productively collaborate in cross-functional teamsExcellent interpersonal communication and written skills for presentations, electronic notebook and report writingAbility to adapt to new and fast-paced environment and navigate uncertaintiesWillingness to embrace new challenges, fearlessly innovate and constantly learn  skills: Molecular Biology, Cell Biology, Biology, Microbiology, 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.Qualified applicants in San Francisco with criminal histories will be considered for employment in accordance with the San Francisco Fair Chance Ordinance. We will consider for employment all qualified Applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance. 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 & Development (R&D) group is responsible for everything from research and discovery to post-market clinical development. Research & Development (R&D) involves all bench and clinical research and the associated groups that support those endeavors. Our teams work on developing first-in-class and best-in-class therapeutics that provide meaningful advances to patients who live with rare diseases. Come join our team and make a meaningful impact on patients' lives. We are looking for a highly motivated team member with extensive experience in mammalian cell culture models to be a key contributor to the Research Gene Therapy Group. The incumbent will be responsible for supporting the development of primary, iPSC-derived, and immortalized cell-based models for expression, safety, and functional testing of gene therapy candidates. The incumbent will also execute routine molecular and biochemical analyses and utilize novel state of the art technologies like next generation sequencing. 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: San Rafael, California job type: Contract salary: $42.79 - 50.34 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Perform routine cell culture as well as viral (AAV / LV) and non-viral modification of adherent, suspension, iPSC-derived and primary cell linesDesign, modify, and clone DNA constructs for expression of proteins and fusion proteins in mammalian expression systemsPerform standard molecular biology techniques including DNA extraction, RNA extraction, and PCR / ddPCRApply basic biochemical and immunological techniques, including protein extraction, protein gel electrophoresis, conventional and capillary western blotting, ELISA, and flow cytometryPerform routine molecular biology techniques using the engineered cell lines to support development of new next-generation sequencing (NGS) assays for sequence determination, editing efficiency analysis, and off-target assessmentMaintain detailed records of experimental protocols and data in electronic laboratory notebook in accordance with company policyEffectively collaborate with a fully integrated research team to facilitate the success of projects  qualifications: Bachelor's (BS) degree or Master's (MS) in Molecular Biology, Biochemistry, Synthetic Biology or relevant biological sciencesGene therapy or gene editing experience preferred, including working knowledge of state-of-the-art technologies utilized in the field.Strong technical background with standard laboratory methods, including culturing immortalized, iPSC-derived and primary cells; molecular biology and cloning; (q)PCR; ELISA; intracellular staining; western blotting; DNA transfection and viral transduction; flow cytometry or microscopyAbility to productively collaborate in cross-functional teamsExcellent interpersonal communication and written skills for presentations, electronic notebook and report writingAbility to adapt to new and fast-paced environment and navigate uncertaintiesWillingness to embrace new challenges, fearlessly innovate and constantly learn  skills: Molecular Biology, Cell Biology, Biology, Microbiology, 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.Qualified applicants in San Francisco with criminal histories will be considered for employment in accordance with the San Francisco Fair Chance Ordinance. We will consider for employment all qualified Applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance. 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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