Thank you for subscribing to your personalized job alerts.

    6 jobs found in Spring, Texas

    Filter2
    Clear all
      • Spring, Texas
      • Temp to Perm
      • $18.00 - $21.40 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 GMP regulations- Ability to wear and work in PPEEducation:BachelorsExperience:4-7 yearsQualifications:Bachelor's or Associate's degree in a science related field or equivalent from college or technical schoolExperience working in a GMP facility or pharmaceutical environment Apply today at 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 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 GMP regulations- Ability to wear and work in PPEEducation:BachelorsExperience:4-7 yearsQualifications:Bachelor's or Associate's degree in a science related field or equivalent from college or technical schoolExperience working in a GMP facility or pharmaceutical environment Apply today at 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. The primary purpose of this role is to monitor and organize the Quality Control Lab.Responsibilities:- Quality control of assays- Documentation/administration of data- Write Standard Operating Procedures- Data entry into various software systemsWorking hours: 8:00 AM - 5:00 PMSkills:- 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 PPE- Tech savvyEducation:BachelorsExperience:1-4 yearsQualifications:Bachelor's or Associate's degree or equivalent from college or technical schoolExperience working in a GMP facility or pharmaceutical environment is preferred Apply today at 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 role is to monitor and organize the Quality Control Lab.Responsibilities:- Quality control of assays- Documentation/administration of data- Write Standard Operating Procedures- Data entry into various software systemsWorking hours: 8:00 AM - 5:00 PMSkills:- 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 PPE- Tech savvyEducation:BachelorsExperience:1-4 yearsQualifications:Bachelor's or Associate's degree or equivalent from college or technical schoolExperience working in a GMP facility or pharmaceutical environment is preferred Apply today at 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
      • $22.00 - $40.00 per hour
      • 12:00 AM - 12:00 AM (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 provide software validation and equipment calibration to support 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: 12:00 AM - 12:00 AM (Various Shifts Available)Skills:- 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 at 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 role is to provide software validation and equipment calibration to support 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: 12:00 AM - 12:00 AM (Various Shifts Available)Skills:- 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 at 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
      • $19.00 - $20.00 per hour
      • 12:00 AM - 12:00 AM (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 ensure compliance with regulatory requirements and internal policies in the manufacturing department.Responsibilities:- Review and verify all manufacturing batch documentation, production records, and ensure the documentation complies with regulations and internal quality control practices.- Assist in reviewing and writing Standard Operating Procedures for manufacturing, and protocols for development, Installation Qualification (IQ) and Operational Qualification (OQ) and validations- Assist in routine internal audits, review deviations and investigations- Ensure compliance with Good Manufacturing Practices (GMP's) and Standard Operating Procedures (SOP's)Working hours: 12:00 AM - 12:00 AM (Various Shifts Available)Skills:- Excellent written and oral communication skills- Meticulous organizational skills and demonstrating meticulous documentation and record review practices- Technical writing experienceEducation:BachelorsExperience:1-4 yearsQualifications:- Associate's degree and/or one to three years of relevant experience- Must have previous technical writing experience- Experience working in a GMP facility or pharmaceutical environment is preferred- Experience with microbiology techniques is preferred Apply today at 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 role is to ensure compliance with regulatory requirements and internal policies in the manufacturing department.Responsibilities:- Review and verify all manufacturing batch documentation, production records, and ensure the documentation complies with regulations and internal quality control practices.- Assist in reviewing and writing Standard Operating Procedures for manufacturing, and protocols for development, Installation Qualification (IQ) and Operational Qualification (OQ) and validations- Assist in routine internal audits, review deviations and investigations- Ensure compliance with Good Manufacturing Practices (GMP's) and Standard Operating Procedures (SOP's)Working hours: 12:00 AM - 12:00 AM (Various Shifts Available)Skills:- Excellent written and oral communication skills- Meticulous organizational skills and demonstrating meticulous documentation and record review practices- Technical writing experienceEducation:BachelorsExperience:1-4 yearsQualifications:- Associate's degree and/or one to three years of relevant experience- Must have previous technical writing experience- Experience working in a GMP facility or pharmaceutical environment is preferred- Experience with microbiology techniques is preferred Apply today at 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
      • $20.00 - $25.00 per hour
      • 12:00 AM - 12:00 PM (Various Shifts Available)
      Spherion Staffing has partnered with a bio-pharmaceutical industry leader to recruit for this role. The responsibilities for the position include: QC assays, testing, documentation, QC analysis, and validation.Responsibilities:- QC Assays (ELISA Assays, HPLC Analysis of Plasmid iso-forms, Wet Chemistry Techniques)- Testing- Documentation (write protocols for test method validation and Qualifications, write development reports, validation, and other relevant technical reports)- QC Analysis (HPLC software)- Validation (Qualification of USP/compendia methods, Tech transfer of assays, Test Method validation, Qualification of new equipment)Working hours: 12:00 AM - 12:00 PM (Various Shifts Available)Skills:- Assay development experience- Experience with gPCR is a must- Method development and optimization experience in a cGMP environment a plus- Experience with chromatography, gel electrophoresis, and microbiology techniques are preferredEducation:BachelorsExperience:1-4 yearsQualifications:Candidates should have a Bachelor???s or Associate's degree and 3+ years of relevant experience and 2-5 years of assay development experience Apply today at 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 responsibilities for the position include: QC assays, testing, documentation, QC analysis, and validation.Responsibilities:- QC Assays (ELISA Assays, HPLC Analysis of Plasmid iso-forms, Wet Chemistry Techniques)- Testing- Documentation (write protocols for test method validation and Qualifications, write development reports, validation, and other relevant technical reports)- QC Analysis (HPLC software)- Validation (Qualification of USP/compendia methods, Tech transfer of assays, Test Method validation, Qualification of new equipment)Working hours: 12:00 AM - 12:00 PM (Various Shifts Available)Skills:- Assay development experience- Experience with gPCR is a must- Method development and optimization experience in a cGMP environment a plus- Experience with chromatography, gel electrophoresis, and microbiology techniques are preferredEducation:BachelorsExperience:1-4 yearsQualifications:Candidates should have a Bachelor???s or Associate's degree and 3+ years of relevant experience and 2-5 years of assay development experience Apply today at 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
      • $17.00 - $18.00 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 ensure purity of research and GMP materials.Responsibilities:- Maintain, clean, and sterilize manufacturing equipment- Perform preventative maintenance- Document activities as required for GMP materials- Manage supplies inventoryWorking hours: 6:00 AM - 3:00 PMSkills:- Organization- Attention to detail- DocumentationEducation:High SchoolExperience:0-1 yearsQualifications:High school diploma or general education degree (GED); or one to three months related experience and/or trainingExperience working in a GMP facility or pharmaceutical environment is preferred Apply today at 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 role is to ensure purity of research and GMP materials.Responsibilities:- Maintain, clean, and sterilize manufacturing equipment- Perform preventative maintenance- Document activities as required for GMP materials- Manage supplies inventoryWorking hours: 6:00 AM - 3:00 PMSkills:- Organization- Attention to detail- DocumentationEducation:High SchoolExperience:0-1 yearsQualifications:High school diploma or general education degree (GED); or one to three months related experience and/or trainingExperience working in a GMP facility or pharmaceutical environment is preferred Apply today at 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.

    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.