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 Document Biotechnology & Pharmaceutical jobs found

    Filter2
    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.* Perform preventative maintenance.* Document activities as required for GMP materials.* Manage supplies inventory.Working hours: 6:00 AM - 3:00 PMSkills:* Organization.* Attention to detail.* Scientific documentation.Education: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. 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 inventory.Working hours: 6:00 AM - 3:00 PMSkills:* Organization.* Attention to detail.* Scientific documentation.Education: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. 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.
      • Madison, Wisconsin
      • Temporary
      • $20.00 - $22.00 per hour
      • 8:00 AM - 5:00 PM
      This position can be REMOTE!Spherion is recruiting a Quality Systems Project Associate! In this position, you will be an integral member of the team dedicated to assisting our client in maintaining compliance with key quality system processes.Responsibilities:- Support key day-to-day tasks within the supplier quality team, including supplier change notifications, supplier approvals, and direct material approvals- Perform project assignments to support the supplier quality organization- Modify and create procedures, forms, and records necessary for the quality system- Complete actions assigned from audits, deviations, changes, nonconformances, etc.- Assist in the creation of metrics applicable to review processes and report results and suggestions to management or other stakeholders- Represent the Quality System team in projects, as assigned- Work with QS and/or other process or business leaders on urgent/critical activities or corrective actions needed for the businessWorking hours: 8:00 AM - 5:00 PMSkills:- Excellent organizational skills- Advanced PC skills to include proficiency in Word, Excel, SharePoint, Outlook, and PowerPoint- Good oral and written communication skills- Independent, self-starter with the desire to learn new skills and participate in continuous improvement projectsEducation:AssociateExperience:1-4 yearsQualifications:- Associate degree, Bachelors degree, or relevant experience- Minimum one year of similar or related experience in document control coordination, processing, or record retention role- Experience in quality assurance, with an understanding of quality system processes, preferred- Experience with ERP and electronic quality management system software such as SAP and EtQ software, preferred- High attention to detail Apply via the apply button in the top right hand corner 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.
      This position can be REMOTE!Spherion is recruiting a Quality Systems Project Associate! In this position, you will be an integral member of the team dedicated to assisting our client in maintaining compliance with key quality system processes.Responsibilities:- Support key day-to-day tasks within the supplier quality team, including supplier change notifications, supplier approvals, and direct material approvals- Perform project assignments to support the supplier quality organization- Modify and create procedures, forms, and records necessary for the quality system- Complete actions assigned from audits, deviations, changes, nonconformances, etc.- Assist in the creation of metrics applicable to review processes and report results and suggestions to management or other stakeholders- Represent the Quality System team in projects, as assigned- Work with QS and/or other process or business leaders on urgent/critical activities or corrective actions needed for the businessWorking hours: 8:00 AM - 5:00 PMSkills:- Excellent organizational skills- Advanced PC skills to include proficiency in Word, Excel, SharePoint, Outlook, and PowerPoint- Good oral and written communication skills- Independent, self-starter with the desire to learn new skills and participate in continuous improvement projectsEducation:AssociateExperience:1-4 yearsQualifications:- Associate degree, Bachelors degree, or relevant experience- Minimum one year of similar or related experience in document control coordination, processing, or record retention role- Experience in quality assurance, with an understanding of quality system processes, preferred- Experience with ERP and electronic quality management system software such as SAP and EtQ software, preferred- High attention to detail Apply via the apply button in the top right hand corner 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.
      • College Station, Texas
      • Permanent
      • $21.00 - $23.22 per hour
      • 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 cultivationOperation 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 providedResponsible for learning and applying current Good Manufacturing PracticeWorking hours: Various Shifts AvailableSkills:Excellent oral and written communication skills, interpersonal and organizational skills.Ability to receive training in various filtration and analytical techniquesGood 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 skillsMust possess excellent math and computer skillsSafety and following safety procedures must be a priority.Education:High SchoolExperience:0-1 yearsQualifications:High school diploma/GED, with 1 year of relevant experience; ORAssociates degree in life sciences field with 0 ??? 1 years experience preferredExpress strong interest in a career preferably in Chemistry, Biology, Life Sciences or a related field.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 glovesLift and/or move 25-50 pounds frequently.Attendance is mandatory.Additional working conditions & physical requirements for some positions:No makeup 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 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 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 cultivationOperation 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 providedResponsible for learning and applying current Good Manufacturing PracticeWorking hours: Various Shifts AvailableSkills:Excellent oral and written communication skills, interpersonal and organizational skills.Ability to receive training in various filtration and analytical techniquesGood 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 skillsMust possess excellent math and computer skillsSafety and following safety procedures must be a priority.Education:High SchoolExperience:0-1 yearsQualifications:High school diploma/GED, with 1 year of relevant experience; ORAssociates degree in life sciences field with 0 ??? 1 years experience preferredExpress strong interest in a career preferably in Chemistry, Biology, Life Sciences or a related field.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 glovesLift and/or move 25-50 pounds frequently.Attendance is mandatory.Additional working conditions & physical requirements for some positions:No makeup 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 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

    Thank you for subscribing to your personalized job alerts.

    Explore over 3 jobs

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