Thank you for subscribing to your personalized job alerts.

    4 jobs found in humble, texas

    Filter2
    • Industry1
      Working in
      Show 4 jobs
      Clear filter
    • Location1
      Location & range
        Show 4 jobs
        Clear filter
      • Job types
        Job types
        Show 4 jobs
        Clear filter
      • Salary
        Salary
        $
        Show 4 jobs
        Clear filter
      Clear all
        • Spring, Texas
        • Temp to Perm
        • $22.00 - $30.00 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 role is to provide software validation and equipment calibration support to manufacturing procedures in order to ensure compliance of regulatory guidelines and required specifications.Responsibilities:- Aid the development of validation documentation- Assist in carrying out qualification protocols and writing summary reports- Maintain validation schedules- Support new product expansion as well as process optimization and validation activitiesWorking hours: 8:00 AM - 5:00 PMSkills:- Excellent written and oral communication skills- Ability to analyze and review data- Ability to receive training in current Good Manufacturing Practice regulationsEducation:BachelorsExperience:1-4 yearsQualifications:- Bachelor???s degree and/or one to three years of relevant experience- Experience working in a pharmaceutical environment is preferred- Software validation experience in a cGMP environment is a plus Apply today!Spherion 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 role is to provide software validation and equipment calibration support to manufacturing procedures in order to ensure compliance of regulatory guidelines and required specifications.Responsibilities:- Aid the development of validation documentation- Assist in carrying out qualification protocols and writing summary reports- Maintain validation schedules- Support new product expansion as well as process optimization and validation activitiesWorking hours: 8:00 AM - 5:00 PMSkills:- Excellent written and oral communication skills- Ability to analyze and review data- Ability to receive training in current Good Manufacturing Practice regulationsEducation:BachelorsExperience:1-4 yearsQualifications:- Bachelor???s degree and/or one to three years of relevant experience- Experience working in a pharmaceutical environment is preferred- Software validation experience in a cGMP environment is a plus Apply today!Spherion 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
        • $25.00 - $29.00 per hour
        • 6:00 AM - 3:00 PM
        Spherion Staffing has partnered with a bio-pharmaceutical industry leader to recruit for this role. The primary purpose of this role is to supervise department personnel and manufacture plasmid DNA in accordance with cGMP guidelines.Responsibilities:- Oversee employees in the manufacturing department, including task delegation- Assist in scaling-up processes- Manufacture plasmid DNA, including cell banking as well as the fermentation and purification processes following SOPs and cGMP guidelines- Ensure team is manufacturing plasmid DNA in accordance with cGMP guidelines- Prepare solutions to be used in the manufacturing process- Execute validation protocols as needed- Write Standard Operating Procedures- Install, document, and maintain equipment as neededWorking hours: 6:00 AM - 3:00 PMSkills:- Possess leadership skills- Excellent written and oral communication skills- Ability to work in a clean room environment for extended periods of time- Ability to wear and work in PPEEducation:AssociateExperience:1-4 yearsQualifications:- Bachelor???s or Associate???s degree in a science related field with 3 or more years of cGMP manufacturing experience- Plasmid purification experience, preferred- Knowledge of microbiological techniques, preferred Apply today!Spherion 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 role is to supervise department personnel and manufacture plasmid DNA in accordance with cGMP guidelines.Responsibilities:- Oversee employees in the manufacturing department, including task delegation- Assist in scaling-up processes- Manufacture plasmid DNA, including cell banking as well as the fermentation and purification processes following SOPs and cGMP guidelines- Ensure team is manufacturing plasmid DNA in accordance with cGMP guidelines- Prepare solutions to be used in the manufacturing process- Execute validation protocols as needed- Write Standard Operating Procedures- Install, document, and maintain equipment as neededWorking hours: 6:00 AM - 3:00 PMSkills:- Possess leadership skills- Excellent written and oral communication skills- Ability to work in a clean room environment for extended periods of time- Ability to wear and work in PPEEducation:AssociateExperience:1-4 yearsQualifications:- Bachelor???s or Associate???s degree in a science related field with 3 or more years of cGMP manufacturing experience- Plasmid purification experience, preferred- Knowledge of microbiological techniques, preferred Apply today!Spherion 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
        • $22.00 - $24.00 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 role is to provide software validation and equipment calibration support to manufacturing procedures in order to ensure compliance of regulatory guidelines and required specifications.Responsibilities:- Aid the development of validation documentation- Assist in carrying out qualification protocols and writing summary reports- Maintain validation schedules- Support new product expansion as well as process optimization and validation activitiesWorking hours: 8:00 AM - 5:00 PMSkills:- Excellent written and oral communication skills- Ability to analyze and review data- Ability to receive training in current Good Manufacturing Practice regulationsEducation:AssociateExperience:1-4 yearsQualifications:- Bachelor degree and/or one to three years of relevant experience- Experience working in a pharmaceutical environment is preferred- Software validation experience in a cGMP environment is a plus After applying please continue to monitor your email. Spherion will communicate the next steps in the candidate application process via email.Spherion 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 role is to provide software validation and equipment calibration support to manufacturing procedures in order to ensure compliance of regulatory guidelines and required specifications.Responsibilities:- Aid the development of validation documentation- Assist in carrying out qualification protocols and writing summary reports- Maintain validation schedules- Support new product expansion as well as process optimization and validation activitiesWorking hours: 8:00 AM - 5:00 PMSkills:- Excellent written and oral communication skills- Ability to analyze and review data- Ability to receive training in current Good Manufacturing Practice regulationsEducation:AssociateExperience:1-4 yearsQualifications:- Bachelor degree and/or one to three years of relevant experience- Experience working in a pharmaceutical environment is preferred- Software validation experience in a cGMP environment is a plus After applying please continue to monitor your email. Spherion will communicate the next steps in the candidate application process via email.Spherion 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
        • Temporary
        • $16.00 - $21.00 per hour
        • 6:00 AM - 3:00 PM (Various Shifts Available)
        Spherion Staffing has partnered with a bio-pharmaceutical industry leader to recruit for this role. The primary purpose of this role is to manufacture plasmid DNA in accordance with cGMP guidelines.Responsibilities:- Manufacture plasmid DNA, including cell banking as well as the fermentation and purification processes following SOPs and cGMP guidelines- Prepare solutions to be used in the manufacturing process- Follow validation protocols- Write Standard Operating Procedures- Install, document, and maintain equipment as neededWorking hours: 6:00 AM - 3:00 PM (Various Shifts Available)Skills:- Excellent written and oral communication skills- Ability to work in a clean room environment for extended periods of time- Ability to receive training in current Good Manufacturing Practice regulations- Ability to wear and work in PPEEducation:High SchoolExperience:0-1 yearsQualifications:- Bachelor's or Associate's degree in a science related field - OR High School Diploma with 1+ year of relevant work experience Apply today!Spherion 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 role is to manufacture plasmid DNA in accordance with cGMP guidelines.Responsibilities:- Manufacture plasmid DNA, including cell banking as well as the fermentation and purification processes following SOPs and cGMP guidelines- Prepare solutions to be used in the manufacturing process- Follow validation protocols- Write Standard Operating Procedures- Install, document, and maintain equipment as neededWorking hours: 6:00 AM - 3:00 PM (Various Shifts Available)Skills:- Excellent written and oral communication skills- Ability to work in a clean room environment for extended periods of time- Ability to receive training in current Good Manufacturing Practice regulations- Ability to wear and work in PPEEducation:High SchoolExperience:0-1 yearsQualifications:- Bachelor's or Associate's degree in a science related field - OR High School Diploma with 1+ year of relevant work experience Apply today!Spherion 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.

      Thank you for subscribing to your personalized job alerts.

      It looks like you want to switch your language. This will reset your filters on your current job search.