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3 jobs found for logistics in san diego, california

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    • san diego, california
    • permanent
    • $70,000 - $75,000 per year
    job summary: Clinical Research Associate will support IVD (in vitro diagnostics test) clinical studies.   location: San Diego, California job type: Permanent salary: $70,000 - 75,000 per year work hours: 9 to 5 education: Bachelors   responsibilities: Conduct monitoring visits and activities in accordance with FDA Code of FederalRegulations, GCP guidelines, departmental SOPs, Work Instructions, and the ClinicalMonitoring PlanServe as primary site contact; establish and maintain regular communication with clinical sitesConduct Site-Qualification, Initiation, Interim and Closeout visits to include document review for accurate data recording, source data verification to protocol adherence and governing regulationsAssist with distribution, collection, and tracking of regulatory documents for site compliance and auditPrepare and maintain monitoring visit reports and site communication documentationIdentify and resolve routine site issues, protocol deviations, queries, study discrepancies and collects missing or incomplete informationAssist with sample tracking, supply shipments and other diagnostic requirementsUse of EDC and other electronic tools to review monitor listings and queriesReview of Investigator Site Files and Sponsor Study FilesAdditional project and tasks as determined by department and organizational needsTravel may be approximately 10%  qualifications: Bachelor's Degree2 years of related clinical trial monitoring experienceExperience of IVD clinical studies is preferred  skills: CRF, GCP (Good Clinical Practice), COV (Close-Out Visit), CTMS (Clinical Trial Management Systems), RMV (Routine Monitoring Visit), SIV (Site Initiation Visit) Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com.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: Clinical Research Associate will support IVD (in vitro diagnostics test) clinical studies.   location: San Diego, California job type: Permanent salary: $70,000 - 75,000 per year work hours: 9 to 5 education: Bachelors   responsibilities: Conduct monitoring visits and activities in accordance with FDA Code of FederalRegulations, GCP guidelines, departmental SOPs, Work Instructions, and the ClinicalMonitoring PlanServe as primary site contact; establish and maintain regular communication with clinical sitesConduct Site-Qualification, Initiation, Interim and Closeout visits to include document review for accurate data recording, source data verification to protocol adherence and governing regulationsAssist with distribution, collection, and tracking of regulatory documents for site compliance and auditPrepare and maintain monitoring visit reports and site communication documentationIdentify and resolve routine site issues, protocol deviations, queries, study discrepancies and collects missing or incomplete informationAssist with sample tracking, supply shipments and other diagnostic requirementsUse of EDC and other electronic tools to review monitor listings and queriesReview of Investigator Site Files and Sponsor Study FilesAdditional project and tasks as determined by department and organizational needsTravel may be approximately 10%  qualifications: Bachelor's Degree2 years of related clinical trial monitoring experienceExperience of IVD clinical studies is preferred  skills: CRF, GCP (Good Clinical Practice), COV (Close-Out Visit), CTMS (Clinical Trial Management Systems), RMV (Routine Monitoring Visit), SIV (Site Initiation Visit) Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com.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 diego, california
    • temporary
    • $30 - $50 per hour
    We are now looking for a detail oriented Contracts Specialist to assist with a name change and legal entity reorganization project. This is a hybrid remote and onsite position based at Hologic in San Diego, CA. Schedule is Mon-Fri and normal business hours. Prior work experience with contracts drafting/editing in Salesforce is highly desirable for this role.  Hourly Pay is depending on candidate qualifications and experience. We offer medical, dental and vision insurance benefits via Anthem and a weekly paycheck.  Please call or text me today for more information! Contact Rebecca at 760-444-0798. We look forward to hearing from you!salary: $30 - $50 per hourshift: Firstwork hours: 8 AM - 5 PMeducation: BachelorResponsibilitiesEssential Duties and Responsibilities • Review, draft and formulate standard sales contracts/Amendments • Respond to customer or vendor inquiries regarding name changes and adjustments • Setup vendor profiles • Partner with Contracts Specialists along with Hologic’s internal departments, to support the negotiations of customer contract terms and conditions in connection with internal re-organization, and ensure sales contracts are consistent with Hologic’s terms, conditions, policies and proceduresThe essential functions of this role include:working in a smoke free environmentSkillsSalesForce.com (3 years of experience is preferred)Written CommunicationVerbal CommunicationConfidentialityResponsivenessParalegal CertificateQualificationsYears 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.At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com.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.
    We are now looking for a detail oriented Contracts Specialist to assist with a name change and legal entity reorganization project. This is a hybrid remote and onsite position based at Hologic in San Diego, CA. Schedule is Mon-Fri and normal business hours. Prior work experience with contracts drafting/editing in Salesforce is highly desirable for this role.  Hourly Pay is depending on candidate qualifications and experience. We offer medical, dental and vision insurance benefits via Anthem and a weekly paycheck.  Please call or text me today for more information! Contact Rebecca at 760-444-0798. We look forward to hearing from you!salary: $30 - $50 per hourshift: Firstwork hours: 8 AM - 5 PMeducation: BachelorResponsibilitiesEssential Duties and Responsibilities • Review, draft and formulate standard sales contracts/Amendments • Respond to customer or vendor inquiries regarding name changes and adjustments • Setup vendor profiles • Partner with Contracts Specialists along with Hologic’s internal departments, to support the negotiations of customer contract terms and conditions in connection with internal re-organization, and ensure sales contracts are consistent with Hologic’s terms, conditions, policies and proceduresThe essential functions of this role include:working in a smoke free environmentSkillsSalesForce.com (3 years of experience is preferred)Written CommunicationVerbal CommunicationConfidentialityResponsivenessParalegal CertificateQualificationsYears 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.At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com.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 diego, california
    • permanent
    • $120,000 - $140,000 per year
    job summary: Seeking a talented and motivated individual with expertise in molecular biology and next generation sequencing (NGS) to join a multidisciplinary team dedicated to discovery and productization of novel cell-based immunotherapies. Initially the candidate will develop and perform genome editing assays to support company's gene editing platform and preclinical pipelines. The position will evolve to include establishment of genomic analysis tools for NGS assays used in the manufacturing process and characterization of genetically engineered induced pluripotent stem cells (iPSCs). Candidate is highly desired to master molecular biology techniques and to independently design and deliver high quality results to meet aggressive timelines. 100% on-site work in San Diego, CA   location: San Diego, California job type: Permanent salary: $120,000 - 140,000 per year work hours: 8 to 4 education: Doctorate   responsibilities: Lead the molecular characterization team to develop and execute experimental plans to meet program and corporate research objectives and timelines and to mentor the junior team members.Design, optimize, and qualify molecular biology assays, including but not limited to PCR, qPCR, ddPCR, and sequencing for high-throughput, reliable, and in-depth characterization of genetic profiles of cell products following complicated genome editing experimentsDevelop cutting edge molecular assays with the application of NGS technology, identify creative solutions to problems and invent new methodologies and workflows to improve sequencing technologies.Develop lab automation (liquid handlers / plate readers, robotics) as needed for improvement of molecular biology assaysStandardize the methodologies and data analysis to establish statistical criteriaUse expertise and systematic problem-solving methods to troubleshoot and solve complex assay development issuesMust be team-oriented and able to communicate research and development findings in cross-disciplinary team meetings as well as with external partnersRecord detailed experimental procedures in laboratory notebooks and controlled documentsAdditional and incidental duties related to the primary duties may be required from time to time.  qualifications: Ph.D. degree in Molecular Biology or related fields plus 5+ years of analytical development experience. Industrial experience is desirable.Expertise in CRISPR-Cas genome editing and molecular and genomic assays for characterization is required.Experience in NGS methodologies is preferred; experience in Nanopore platforms a plus.Experience in managing the team and projects is preferred.Experience in lab automation is preferable.Experience in bioinformatics, NGS data analysis, and scientific programming in data analysis tools, e.g. Python, R, ImageJ, JMP, is a plus.Desire to understand the fundamental aspect of technologies, and the ability to identify creative solutions to overcome current limitations.Ability to design, implement, analyze, and present experiments to demonstrate feasibility of new methods and efficiently move products through pipelineSelf-motivated, strong problem-solving ability, organizational skills, and attention to detailsComfortable in a fast-paced environment and able to adjust workload based upon changing priorities.Excellent communication and presentation skills. Working Conditions and Physical Requirements Will require working with blood and cell lines of human and animal originWill require working with hazardous materialsOccasional evening and weekend work will be required Benefits include: Medical, dental, vision, flex spending accounts, life insurance, disability, supplemental health, EAP, and travel assistance program This is a salaried position with a 12.5%-15% bonus target as well as RSU's.   skills: Molecular Biology, Data Analysis, Assay Development Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com.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: Seeking a talented and motivated individual with expertise in molecular biology and next generation sequencing (NGS) to join a multidisciplinary team dedicated to discovery and productization of novel cell-based immunotherapies. Initially the candidate will develop and perform genome editing assays to support company's gene editing platform and preclinical pipelines. The position will evolve to include establishment of genomic analysis tools for NGS assays used in the manufacturing process and characterization of genetically engineered induced pluripotent stem cells (iPSCs). Candidate is highly desired to master molecular biology techniques and to independently design and deliver high quality results to meet aggressive timelines. 100% on-site work in San Diego, CA   location: San Diego, California job type: Permanent salary: $120,000 - 140,000 per year work hours: 8 to 4 education: Doctorate   responsibilities: Lead the molecular characterization team to develop and execute experimental plans to meet program and corporate research objectives and timelines and to mentor the junior team members.Design, optimize, and qualify molecular biology assays, including but not limited to PCR, qPCR, ddPCR, and sequencing for high-throughput, reliable, and in-depth characterization of genetic profiles of cell products following complicated genome editing experimentsDevelop cutting edge molecular assays with the application of NGS technology, identify creative solutions to problems and invent new methodologies and workflows to improve sequencing technologies.Develop lab automation (liquid handlers / plate readers, robotics) as needed for improvement of molecular biology assaysStandardize the methodologies and data analysis to establish statistical criteriaUse expertise and systematic problem-solving methods to troubleshoot and solve complex assay development issuesMust be team-oriented and able to communicate research and development findings in cross-disciplinary team meetings as well as with external partnersRecord detailed experimental procedures in laboratory notebooks and controlled documentsAdditional and incidental duties related to the primary duties may be required from time to time.  qualifications: Ph.D. degree in Molecular Biology or related fields plus 5+ years of analytical development experience. Industrial experience is desirable.Expertise in CRISPR-Cas genome editing and molecular and genomic assays for characterization is required.Experience in NGS methodologies is preferred; experience in Nanopore platforms a plus.Experience in managing the team and projects is preferred.Experience in lab automation is preferable.Experience in bioinformatics, NGS data analysis, and scientific programming in data analysis tools, e.g. Python, R, ImageJ, JMP, is a plus.Desire to understand the fundamental aspect of technologies, and the ability to identify creative solutions to overcome current limitations.Ability to design, implement, analyze, and present experiments to demonstrate feasibility of new methods and efficiently move products through pipelineSelf-motivated, strong problem-solving ability, organizational skills, and attention to detailsComfortable in a fast-paced environment and able to adjust workload based upon changing priorities.Excellent communication and presentation skills. Working Conditions and Physical Requirements Will require working with blood and cell lines of human and animal originWill require working with hazardous materialsOccasional evening and weekend work will be required Benefits include: Medical, dental, vision, flex spending accounts, life insurance, disability, supplemental health, EAP, and travel assistance program This is a salaried position with a 12.5%-15% bonus target as well as RSU's.   skills: Molecular Biology, Data Analysis, Assay Development Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com.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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