You are successfully logged out of your my randstad account

You have successfully deleted your account

    Thank you for subscribing to your personalized job alerts.

    4 jobs found for Lab in Texas

    Filter3
    Clear all
      • 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.*Maintain highest standard of clean room environment in order to ensure purity of lab work.*Perform preventative maintenance.*Document activities for GMP materials.*Manage supplies inventory.Working 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 training*Experience working in a GMP facility or pharmaceutical environment is 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. The primary purpose of this role is to ensure purity of research and GMP materials.Responsibilities:*Maintain, clean, and sterilize manufacturing equipment.*Maintain highest standard of clean room environment in order to ensure purity of lab work.*Perform preventative maintenance.*Document activities for GMP materials.*Manage supplies inventory.Working 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 training*Experience working in a GMP facility or pharmaceutical environment is 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.
      • 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.*Ensure highest quality team work completed during manufacture of plasmid DNA.*Assist in scaling-up processes.*Manufacture plasmid DNA.*Cell banking and fermentation following SOPs and cGMP guidelines.* Purification processes following SOPs and cGMP guidelines.* Ensure team is working in accordance with cGMP guidelines.* Prepare solutions to be used in the manufacturing process.*Implement validation protocols.*Write SOPs.*Lab equipment maintenance.Working hours: 6:00 AM - 3:00 PMSkills:*Established expertise in biological science or related life sciences. *Possess leadership skills and the ability to lead a team in a laboratory setting.*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 PPE.Education:AssociateExperience:1-4 yearsQualifications:* Bachelors or Associates degree in a life science related field with 3 or more years of cGMP manufacturing experience* Plasmid purification experience* Knowledge of microbiological techniques 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 supervise department personnel and manufacture plasmid DNA in accordance with cGMP guidelines.Responsibilities:*Oversee employees.*Ensure highest quality team work completed during manufacture of plasmid DNA.*Assist in scaling-up processes.*Manufacture plasmid DNA.*Cell banking and fermentation following SOPs and cGMP guidelines.* Purification processes following SOPs and cGMP guidelines.* Ensure team is working in accordance with cGMP guidelines.* Prepare solutions to be used in the manufacturing process.*Implement validation protocols.*Write SOPs.*Lab equipment maintenance.Working hours: 6:00 AM - 3:00 PMSkills:*Established expertise in biological science or related life sciences. *Possess leadership skills and the ability to lead a team in a laboratory setting.*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 PPE.Education:AssociateExperience:1-4 yearsQualifications:* Bachelors or Associates degree in a life science related field with 3 or more years of cGMP manufacturing experience* Plasmid purification experience* Knowledge of microbiological techniques 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.
      • Bryan, Texas
      • Permanent
      • $25.00 - $37.00 per hour
      • Various Shifts Available
      Spherion Staffing has partnered with a leading biotechnology company in College Station, TX to recruit for this role. The primary purpose of this role is to provide hands-on support in either the Upstream or Downstream department. This role will be responsible for working in various manufacturing operations such as vaccine and therapeutic production in accordance with GMP (good manufacturing practice) regulations.Responsibilities:?? Upstream manufacturing duties include: overseeing cell cultivation process, plate counting, microscopic examination, banking of cell lines and viruses, operating bacterial fermentation culture vessels, and operating bioreactors?? Downstream manufacturing duties include: overseeing filtration and purification processes by working with various filtration systems (e.g. Tangential Flow Filtration, nanofiltration and depth filtration), chromatographic systems, and aseptic process simulation and drug product filling?? 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 according to cGMP regulations, and ensure other team members are trained.?? Perform lab maintenance duties by assisting with daily cleaning and sanitizing of sterile production areas.Working hours: Various Shifts AvailableSkills:- Excellent oral and written communication skills, interpersonal and organizational skills.- Strong leadership skills and ability to provide training to others on cGMP regulations- Good self-discipline and attention to detail.- Must be able to work 12-hour shift and be willing to work outside of normal, scheduled hours; as necessary.- Experience working in a cleanroom environment in full sterile room gowning and good aseptic technique.- Possess effective time management and organizational skills- Must possess excellent math and computer skills- Safety and following safety procedures must be a priority.Education:AssociateExperience:1-4 yearsQualifications:Associate's Degree or Bachelor's Degree in Life Sciences or other related field AND 2-4 years of relevant experience, with at least 1 year GMP experience.The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this 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. Apply online today and a recruiter will review your information and reach out to schedule an interview!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, Relig
      Spherion Staffing has partnered with a leading biotechnology company in College Station, TX to recruit for this role. The primary purpose of this role is to provide hands-on support in either the Upstream or Downstream department. This role will be responsible for working in various manufacturing operations such as vaccine and therapeutic production in accordance with GMP (good manufacturing practice) regulations.Responsibilities:?? Upstream manufacturing duties include: overseeing cell cultivation process, plate counting, microscopic examination, banking of cell lines and viruses, operating bacterial fermentation culture vessels, and operating bioreactors?? Downstream manufacturing duties include: overseeing filtration and purification processes by working with various filtration systems (e.g. Tangential Flow Filtration, nanofiltration and depth filtration), chromatographic systems, and aseptic process simulation and drug product filling?? 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 according to cGMP regulations, and ensure other team members are trained.?? Perform lab maintenance duties by assisting with daily cleaning and sanitizing of sterile production areas.Working hours: Various Shifts AvailableSkills:- Excellent oral and written communication skills, interpersonal and organizational skills.- Strong leadership skills and ability to provide training to others on cGMP regulations- Good self-discipline and attention to detail.- Must be able to work 12-hour shift and be willing to work outside of normal, scheduled hours; as necessary.- Experience working in a cleanroom environment in full sterile room gowning and good aseptic technique.- Possess effective time management and organizational skills- Must possess excellent math and computer skills- Safety and following safety procedures must be a priority.Education:AssociateExperience:1-4 yearsQualifications:Associate's Degree or Bachelor's Degree in Life Sciences or other related field AND 2-4 years of relevant experience, with at least 1 year GMP experience.The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this 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. Apply online today and a recruiter will review your information and reach out to schedule an interview!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, Relig
      • Spring, Texas
      • Temp to Perm
      • $19.00 - $20.00 per hour
      • 8:00 AM - 5:00 AM
      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 all batch documentation.*Review production records. *Endorse documentation in compliance with regulations and company QC guidelines.*Assist in reviewing and writing SOPs for manufacturing.* Write and review protocols for development, Installation Qualification and Operational Qualification.*Write and review protocol validations.*Assist in routine company audits.*Review deviations and investigations.*Write and review protocols for development reports.* Ensure compliance with GMPs SOPs.Working hours: 8:00 AM - 5:00 AMSkills:*Excellent written and oral communication skills.*Meticulous organizational skills.*Meticulous documentation and record review practices.*Technical writing experience.Education:BachelorsExperience:1-4 yearsQualifications:*Associate's degree and/or one to three years of relevant experience.*Must have previous technical writing experience in a lab setting. *Experience working in a GMP facility or pharmaceutical environment.*Biology or related life sciences as related to manufacture of plasmid DNA. 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 all batch documentation.*Review production records. *Endorse documentation in compliance with regulations and company QC guidelines.*Assist in reviewing and writing SOPs for manufacturing.* Write and review protocols for development, Installation Qualification and Operational Qualification.*Write and review protocol validations.*Assist in routine company audits.*Review deviations and investigations.*Write and review protocols for development reports.* Ensure compliance with GMPs SOPs.Working hours: 8:00 AM - 5:00 AMSkills:*Excellent written and oral communication skills.*Meticulous organizational skills.*Meticulous documentation and record review practices.*Technical writing experience.Education:BachelorsExperience:1-4 yearsQualifications:*Associate's degree and/or one to three years of relevant experience.*Must have previous technical writing experience in a lab setting. *Experience working in a GMP facility or pharmaceutical environment.*Biology or related life sciences as related to manufacture of plasmid DNA. 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.

    Explore over 4 jobs in Texas

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