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    6 jobs found for Manufacturing in Texas

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      • College Station, Texas
      • Permanent
      • $19.00 - $22.00 per hour
      • 6:00 AM - 6:00 PM (Various Shifts Available)
      Spherion Staffing has partnered with FUJIFILM Diosynth Biotechnologies to recruit for this role. This is an exciting opportunity to be a part of the cutting-edge project of COVID-19 vaccine production. The primary purpose of this role is to provide hands-on support in either the Upstream or Downstream department, working in various manufacturing operations such as vaccine and therapeutic production.Responsibilities:- Opportunity to work with protein purification, various filtration systems, and cell cultivation- Operation of general production equipment e.g. Autoclaves, glass washers, incubators, scales, pH/conductivity meters, etc.- Assisting with writing batch production records, Standard Operating Procedures, and document and maintain activity records, training provided- Responsible for learning and applying current Good Manufacturing PracticeWorking hours: 6:00 AM - 6:00 PM (Various Shifts Available)Skills:- Excellent oral and written communication skills, interpersonal and organizational skills.- Ability to receive training in various filtration and analytical techniques- Good self-discipline and attention to detail.- Must be able to work flexible work hours, and be willing to work outside of normal, scheduled hours; as necessary. - Must be able to work alternative shift hours and weekends as required.- Possess effective time management and organizational skills- Must possess excellent math and computer skills- Safety and following safety procedures must be a priority.Education:High SchoolExperience:0-1 yearsQualifications:- Must express strong interest in a career preferably in Chemistry, Biology, Life Sciences or related fieldThe physical demands described here are representative of those that must be met by an employee tosuccessfully perform the essential functions of this job. Reasonable accommodations may be made toenable individuals with disabilities to perform the essential functions. While performing the duties ofthis job, the employee is regularly required to:- Experience prolonged standing, bending, stooping, twisting, and stretching.- Possess hand-eye coordination and manual dexterity sufficient to operate in a laboratory, manufacturing, and/or office environment is required.- Ability to wear personal protective equipment including safety glasses, lab coat, safety shoes and gloves- Lift and/or move 25-50 pounds frequently.- Attendance is mandatory.Additional working conditions & physical requirements for some positions:- No make-up or jewelry can be worn when working in the clean room environment.- Handle and work with potentially hazardous materials and chemicals per OSHA guidelines. Please apply and a recruiter will reach out to schedule an interview after reviewing your application!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. Whether you're looking for temporary, temp-to-perm or direct hire opportunities, 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 FUJIFILM Diosynth Biotechnologies to recruit for this role. This is an exciting opportunity to be a part of the cutting-edge project of COVID-19 vaccine production. The primary purpose of this role is to provide hands-on support in either the Upstream or Downstream department, working in various manufacturing operations such as vaccine and therapeutic production.Responsibilities:- Opportunity to work with protein purification, various filtration systems, and cell cultivation- Operation of general production equipment e.g. Autoclaves, glass washers, incubators, scales, pH/conductivity meters, etc.- Assisting with writing batch production records, Standard Operating Procedures, and document and maintain activity records, training provided- Responsible for learning and applying current Good Manufacturing PracticeWorking hours: 6:00 AM - 6:00 PM (Various Shifts Available)Skills:- Excellent oral and written communication skills, interpersonal and organizational skills.- Ability to receive training in various filtration and analytical techniques- Good self-discipline and attention to detail.- Must be able to work flexible work hours, and be willing to work outside of normal, scheduled hours; as necessary. - Must be able to work alternative shift hours and weekends as required.- Possess effective time management and organizational skills- Must possess excellent math and computer skills- Safety and following safety procedures must be a priority.Education:High SchoolExperience:0-1 yearsQualifications:- Must express strong interest in a career preferably in Chemistry, Biology, Life Sciences or related fieldThe physical demands described here are representative of those that must be met by an employee tosuccessfully perform the essential functions of this job. Reasonable accommodations may be made toenable individuals with disabilities to perform the essential functions. While performing the duties ofthis job, the employee is regularly required to:- Experience prolonged standing, bending, stooping, twisting, and stretching.- Possess hand-eye coordination and manual dexterity sufficient to operate in a laboratory, manufacturing, and/or office environment is required.- Ability to wear personal protective equipment including safety glasses, lab coat, safety shoes and gloves- Lift and/or move 25-50 pounds frequently.- Attendance is mandatory.Additional working conditions & physical requirements for some positions:- No make-up or jewelry can be worn when working in the clean room environment.- Handle and work with potentially hazardous materials and chemicals per OSHA guidelines. Please apply and a recruiter will reach out to schedule an interview after reviewing your application!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. Whether you're looking for temporary, temp-to-perm or direct hire opportunities, 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
      • $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.
      • 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
      • $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
      • $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.

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