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 College Biotechnology & Pharmaceutical jobs found

    Filter3
    Clear all
      • 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 QC Technician is responsible for in-process and release testing of products manufactured.Responsibilities:* Set up organization and daily operations of QC lab* Organization and documentation of data* Write reports, SOPs, and Protocols* QC analysis * Responsible for one or more QC assays (pH, Endotoxin, Gel electrophoresis)Working hours: 8:00 AM - 5:00 PMSkills:* HPLC software* Gel imaging software* Calibration and preventative maintenance of equipment* Record keeping* Attention to detailEducation:AssociateExperience:1-4 yearsQualifications:Bachelor's or Associate's degree or equivalent from college or technical school; or two to three years related experience and/or training; or equivalent combination of education and experience. Apply 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 QC Technician is responsible for in-process and release testing of products manufactured.Responsibilities:* Set up organization and daily operations of QC lab* Organization and documentation of data* Write reports, SOPs, and Protocols* QC analysis * Responsible for one or more QC assays (pH, Endotoxin, Gel electrophoresis)Working hours: 8:00 AM - 5:00 PMSkills:* HPLC software* Gel imaging software* Calibration and preventative maintenance of equipment* Record keeping* Attention to detailEducation:AssociateExperience:1-4 yearsQualifications:Bachelor's or Associate's degree or equivalent from college or technical school; or two to three years related experience and/or training; or equivalent combination of education and experience. Apply 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.
      • College Station, Texas
      • Temporary
      • $18.00 per hour
      • 8:00 AM - 5:00 PM
      Spherion Staffing has partnered with a leading biopharmaceutical manufacturer in College Station, TX to recruit for this role. The primary purpose of this role is to support client audits, regulatory inspections, and internal audits.Responsibilities:Work collaboratively with site management team to promote a `Quality Culture? by coaching other team members on the application of Good Manufacturing Principles (GMP) principles, including the underlying rationale of those principlesProvide support during the internal audits and client audits/inspections.Work with Quality management to ensure quality systems support manufacturing of pre-clinical to commercial products.Provide support for the internal and external Audit Programs to be in an acceptable state of compliance, by conducting audit preparations, internal audits, and assisting client audits with site documentation. Ensure no overdue training or site actions for self and other QA team members.All other duties as may be assigned.Working hours: 8:00 AM - 5:00 PMSkills:GMP knowledge and a degree in Biology, Chemistry, or Engineering.Education:High SchoolExperience:0-1 yearsQualifications:High school diploma with some relevant industry experience OR an Associates Degree in Life Sciences/Engineering field. Preferred qualifications: GMP knowledge and a degree in Biology, Chemistry, or Engineering.Strong written, verbal and interpersonal communications skills. Must be able to write reports and review data.Experience with problem solving with excellent analytical and organizational skills. Working knowledge of MS Office products (Word, Excel, Outlook, PowerPoint). Please apply online today! A recruiter will review your application and then 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, 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 leading biopharmaceutical manufacturer in College Station, TX to recruit for this role. The primary purpose of this role is to support client audits, regulatory inspections, and internal audits.Responsibilities:Work collaboratively with site management team to promote a `Quality Culture? by coaching other team members on the application of Good Manufacturing Principles (GMP) principles, including the underlying rationale of those principlesProvide support during the internal audits and client audits/inspections.Work with Quality management to ensure quality systems support manufacturing of pre-clinical to commercial products.Provide support for the internal and external Audit Programs to be in an acceptable state of compliance, by conducting audit preparations, internal audits, and assisting client audits with site documentation. Ensure no overdue training or site actions for self and other QA team members.All other duties as may be assigned.Working hours: 8:00 AM - 5:00 PMSkills:GMP knowledge and a degree in Biology, Chemistry, or Engineering.Education:High SchoolExperience:0-1 yearsQualifications:High school diploma with some relevant industry experience OR an Associates Degree in Life Sciences/Engineering field. Preferred qualifications: GMP knowledge and a degree in Biology, Chemistry, or Engineering.Strong written, verbal and interpersonal communications skills. Must be able to write reports and review data.Experience with problem solving with excellent analytical and organizational skills. Working knowledge of MS Office products (Word, Excel, Outlook, PowerPoint). Please apply online today! A recruiter will review your application and then 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, 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.
      • College Station, 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;OR High School Diploma AND 3-6 years of relevant experience, with at least 2 years of 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. Please apply online today and a recruiter will reach out once your information has been reviewed, and schedule you for 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 s
      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;OR High School Diploma AND 3-6 years of relevant experience, with at least 2 years of 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. Please apply online today and a recruiter will reach out once your information has been reviewed, and schedule you for 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 s
      • College Station, Texas
      • Permanent
      • $19.00 - $23.00 per hour
      • Various Shifts Available
      Spherion Staffing has partnered with a growing dietary supplements manufacturing facility in College Station, TX to recruit for this role. The primary purpose of this role is to provide hands-on support in the cGMP fermentation facility and work on the manufacture of proprietary microorganisms.Responsibilities:Responsibilities: Prepare production media and buffers, sterilize equipment, operate bioreactors, and perform seed scale-up from lab pilot to production scale.Assist with production equipment maintenance, including cleaning, preventative maintenance, and optimizationEnsure work is completed in compliance with all SOP???s, batch records, controlled documentation, and all applicable regulations, guidelines, safety policies and proceduresParticipate in cleaning and equipment validation efforts as well as validation documents within a cGMP facility.Author, review, and revise deviations/CAPA???s, manufacturing and process equipment documentation, and other technical documentation, as necessary.Operate and use all equipment and chemicals in a safe manner.Participate in cross-training initiatives and assist with training manufacturing associates when needed.Maintain accurate and timely record of equipment service records, and work collaboratively with various departments to compile, analyze, and interpret data.Manage the cycle count process, and ensure cycle counting of the warehouse inventory are accurate and on time.Ensure that the shipping schedule is correctly implemented and report any deviations to Customer Service.Operate in a sterile environment and ensure there is no cross contamination.Develop and maintain proper bacterial management practices to ensure consistent microbial cell culture that meet quality standards and keep pace with desired production goals.Working hours: Various Shifts AvailableSkills:Excellent oral and written communication skills, interpersonal and organizational skills. Good self-discipline and attention to detail.Must possess strong work ethic and prioritization skills. 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:High SchoolExperience:0-1 yearsQualifications:Associate's Degree or Bachelor's Degree in Life Sciences or other related field AND 0-1 years of relevant experience; OR High School Diploma or equivalency with 1-2 years of previous mechanical experience (vehicle shop, machine shop, fabrication shop)**Must possess a valid US Driver???s license Preferred:Previous fermentation experience (including centrifugation) strongly preferred.Previous experience maintaining large pieces of machinery Previous experience with liquid processing equipment (pumps, valves, mixers, heating, cooling, etc.)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 60 lbs. Must be able to tolerate the noise and odor that results from microbial cell culture.?? 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. Work Hours:Must be able to work 12 hour shifts, 1st, 2nd, or 3rd shift Please apply online today! Once you have applied, you will receive a pre screen to complete, and then a recruiter will review your information and contact you 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, 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 growing dietary supplements manufacturing facility in College Station, TX to recruit for this role. The primary purpose of this role is to provide hands-on support in the cGMP fermentation facility and work on the manufacture of proprietary microorganisms.Responsibilities:Responsibilities: Prepare production media and buffers, sterilize equipment, operate bioreactors, and perform seed scale-up from lab pilot to production scale.Assist with production equipment maintenance, including cleaning, preventative maintenance, and optimizationEnsure work is completed in compliance with all SOP???s, batch records, controlled documentation, and all applicable regulations, guidelines, safety policies and proceduresParticipate in cleaning and equipment validation efforts as well as validation documents within a cGMP facility.Author, review, and revise deviations/CAPA???s, manufacturing and process equipment documentation, and other technical documentation, as necessary.Operate and use all equipment and chemicals in a safe manner.Participate in cross-training initiatives and assist with training manufacturing associates when needed.Maintain accurate and timely record of equipment service records, and work collaboratively with various departments to compile, analyze, and interpret data.Manage the cycle count process, and ensure cycle counting of the warehouse inventory are accurate and on time.Ensure that the shipping schedule is correctly implemented and report any deviations to Customer Service.Operate in a sterile environment and ensure there is no cross contamination.Develop and maintain proper bacterial management practices to ensure consistent microbial cell culture that meet quality standards and keep pace with desired production goals.Working hours: Various Shifts AvailableSkills:Excellent oral and written communication skills, interpersonal and organizational skills. Good self-discipline and attention to detail.Must possess strong work ethic and prioritization skills. 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:High SchoolExperience:0-1 yearsQualifications:Associate's Degree or Bachelor's Degree in Life Sciences or other related field AND 0-1 years of relevant experience; OR High School Diploma or equivalency with 1-2 years of previous mechanical experience (vehicle shop, machine shop, fabrication shop)**Must possess a valid US Driver???s license Preferred:Previous fermentation experience (including centrifugation) strongly preferred.Previous experience maintaining large pieces of machinery Previous experience with liquid processing equipment (pumps, valves, mixers, heating, cooling, etc.)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 60 lbs. Must be able to tolerate the noise and odor that results from microbial cell culture.?? 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. Work Hours:Must be able to work 12 hour shifts, 1st, 2nd, or 3rd shift Please apply online today! Once you have applied, you will receive a pre screen to complete, and then a recruiter will review your information and contact you 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, 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 3 jobs in Texas

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