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      • Spring, Texas
      • Temp to Perm
      • $20.00 - $25.00 per hour
      • 8:00 AM - 5:00 PM
      Spherion Staffing has partnered with a bio-pharmaceutical industry leader to recruit for this role. The primary purpose of this position is assay assessment, development, implementation, and validation for use evaluating human biologic drug products manufactured in a cGMP lab. Must be up to date on all methods for QC testing. Set-up, organization, and day to day operations of a QC laboratory.Responsibilities:*Must be able to organize all accumulated data*Keep notebooks up to date and signed*Write protocols for test method validation*Write development reports, validation, and all other relevant technical reports*Write SOPs, testing records, protocols*Responsible for in-process testing*Responsible for release testing*Responsible for stability testing. *Responsible for Method Qualification and Validation.*Must be able to Qualify USP/compendia methods*Responsible for transfer of assays, test method validation, and qualification of new equipment.Working hours: 8:00 AM - 5:00 PMSkills:*Gel electrophoresis*ELISA assays'*HPLC Analysis of Plasmid iso-forms*qPCR gene expression and genomic *Mammalian cell culture and transfection*Wet Chemistry* Experience with Spectramax, qPCR software, HPLC software, Gel imaging software.Education:BachelorsExperience:4-7 yearsQualifications:*Life Sciences Bachelor's degree and 3+ years of relevant experience in molecular biology, microbiology, or chemistry. *2-5 years of assay development experience.*Experience with qPCR is required*Experience with chromatography, gel electrolysis, and microbiology techniques *Method development and optimization in a cGMP environment www.spherion.com/applySpherion has helped thousands of people just like you find work happiness! Our experienced staff will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. No one works harder for you than Spherion. EEO Employer: Race, Religion, Color, National Origin, Citizenship, Sex, Sexual Orientation, Gender Identity, Age, Disability, Ancestry, Veteran Status, Genetic Information, Service in the Uniformed Services or any other classification protected by law.
      Spherion Staffing has partnered with a bio-pharmaceutical industry leader to recruit for this role. The primary purpose of this position is assay assessment, development, implementation, and validation for use evaluating human biologic drug products manufactured in a cGMP lab. Must be up to date on all methods for QC testing. Set-up, organization, and day to day operations of a QC laboratory.Responsibilities:*Must be able to organize all accumulated data*Keep notebooks up to date and signed*Write protocols for test method validation*Write development reports, validation, and all other relevant technical reports*Write SOPs, testing records, protocols*Responsible for in-process testing*Responsible for release testing*Responsible for stability testing. *Responsible for Method Qualification and Validation.*Must be able to Qualify USP/compendia methods*Responsible for transfer of assays, test method validation, and qualification of new equipment.Working hours: 8:00 AM - 5:00 PMSkills:*Gel electrophoresis*ELISA assays'*HPLC Analysis of Plasmid iso-forms*qPCR gene expression and genomic *Mammalian cell culture and transfection*Wet Chemistry* Experience with Spectramax, qPCR software, HPLC software, Gel imaging software.Education:BachelorsExperience:4-7 yearsQualifications:*Life Sciences Bachelor's degree and 3+ years of relevant experience in molecular biology, microbiology, or chemistry. *2-5 years of assay development experience.*Experience with qPCR is required*Experience with chromatography, gel electrolysis, and microbiology techniques *Method development and optimization in a cGMP environment www.spherion.com/applySpherion has helped thousands of people just like you find work happiness! Our experienced staff will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. No one works harder for you than Spherion. EEO Employer: Race, Religion, Color, National Origin, Citizenship, Sex, Sexual Orientation, Gender Identity, Age, Disability, Ancestry, Veteran Status, Genetic Information, Service in the Uniformed Services or any other classification protected by law.
      • Spring, Texas
      • Temp to Perm
      • $18.00 - $20.00 per hour
      • 8:00 AM - 5:00 PM
      Spherion Staffing has partnered with a bio-pharmaceutical industry leader to recruit for this role. Responsible for the maintenance, cleaning, and sterilization of equipment, supplies, and production areas.Responsibilities:* Wash glassware, plastic supplies, and other supporting equipment in a washer or by hand,as needed.* Sterilize materials to support PD/HD manufacture, testing and research.* Weekly and daily cleaning and disinfection of the PD production areas,including documentation of cleaning performed.* Restock main supplies in Production Areas*Perform basic in-process yield analysis of PD and MFG samples, including Miniprep andGel ElectrophoresisWorking hours: 8:00 AM - 5:00 PMSkills:*Lab maintenance and care*Clean room experienceEducation:High SchoolExperience:0-1 yearsQualifications:*1-3 Months related experience or training*Life Sciences background preferred. www.spherion.com/applySpherion has helped thousands of people just like you find work happiness! Our experienced staff will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. No one works harder for you than Spherion. EEO Employer: Race, Religion, Color, National Origin, Citizenship, Sex, Sexual Orientation, Gender Identity, Age, Disability, Ancestry, Veteran Status, Genetic Information, Service in the Uniformed Services or any other classification protected by law.
      Spherion Staffing has partnered with a bio-pharmaceutical industry leader to recruit for this role. Responsible for the maintenance, cleaning, and sterilization of equipment, supplies, and production areas.Responsibilities:* Wash glassware, plastic supplies, and other supporting equipment in a washer or by hand,as needed.* Sterilize materials to support PD/HD manufacture, testing and research.* Weekly and daily cleaning and disinfection of the PD production areas,including documentation of cleaning performed.* Restock main supplies in Production Areas*Perform basic in-process yield analysis of PD and MFG samples, including Miniprep andGel ElectrophoresisWorking hours: 8:00 AM - 5:00 PMSkills:*Lab maintenance and care*Clean room experienceEducation:High SchoolExperience:0-1 yearsQualifications:*1-3 Months related experience or training*Life Sciences background preferred. www.spherion.com/applySpherion has helped thousands of people just like you find work happiness! Our experienced staff will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. No one works harder for you than Spherion. EEO Employer: Race, Religion, Color, National Origin, Citizenship, Sex, Sexual Orientation, Gender Identity, Age, Disability, Ancestry, Veteran Status, Genetic Information, Service in the Uniformed Services or any other classification protected by law.

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