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    6 Temp to Perm jobs found in Spring

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      • Spring, Texas
      • Temp to Perm
      • $15.00 - $18.00 per hour
      • 8:00 AM - 5:00 PM
      Spherion has partnered with a local company in The Woodlands, Texas for an Accounting Clerk. Our ideal candidate has a natural passion for math and eagerness to learn more about financial planning, tax planning, and budgeting.Responsibilities:Perform routine clerical accounting duties within a fast-paced finance department, while adhering to established accounting standardsBe a resource for accounts payable and receivableAssist in year-end audit requestsExecute accurate reporting, filing, and database management in multiple systemsSecures financial information by completing database backups, keeping information confidential.Verify and post details of business transactions, such as funds received and disbursed, and totals accounts to ledgers and databasesWorking hours: 8:00 AM - 5:00 PMSkills:Natural proficiency with mathKnowledge of basic financial, tax, and accounting principlesExcellent organizational skills and attention to detailProficient in Microsoft Office with aptitude to learn new systemsEducation:BachelorsExperience:1-4 yearsQualifications:Bachelor???s degree in finance or accounting Apply now!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 has partnered with a local company in The Woodlands, Texas for an Accounting Clerk. Our ideal candidate has a natural passion for math and eagerness to learn more about financial planning, tax planning, and budgeting.Responsibilities:Perform routine clerical accounting duties within a fast-paced finance department, while adhering to established accounting standardsBe a resource for accounts payable and receivableAssist in year-end audit requestsExecute accurate reporting, filing, and database management in multiple systemsSecures financial information by completing database backups, keeping information confidential.Verify and post details of business transactions, such as funds received and disbursed, and totals accounts to ledgers and databasesWorking hours: 8:00 AM - 5:00 PMSkills:Natural proficiency with mathKnowledge of basic financial, tax, and accounting principlesExcellent organizational skills and attention to detailProficient in Microsoft Office with aptitude to learn new systemsEducation:BachelorsExperience:1-4 yearsQualifications:Bachelor???s degree in finance or accounting Apply now!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.
      • 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.
      • Spring, Texas
      • Temp to Perm
      • $23.00 - $25.00 per hour
      • 8:00 AM - 5:00 PM
      Spherion Staffing has partnered with a local bio-pharmaceutical industry leader to recruit for this role. The primary purpose of this position is to ensure quality assurance and compliance activities. This person will be responsible for production, testing, and associated documentation is within industry guidelines.Responsibilities:* Assemble applicable documentation. * Process CAPAs and perform routine internal audits and maintain quality control.* Maintaining supplier files and audits.* Proper documentation of equipment. * Training new employees.* Develop quality system SOPs.* Inventory Products. * Follow (GMPs) and (SOPs).* Review and approve Analysis Certificates.* Print and approve product labels.Working hours: 8:00 AM - 5:00 PMSkills:*Plasmid purification and microbiology techniques. *Quality Assurance documentation.Education:BachelorsExperience:4-7 yearsQualifications:*GMP experience.*Bachelors degree in applicable life science field. 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 local bio-pharmaceutical industry leader to recruit for this role. The primary purpose of this position is to ensure quality assurance and compliance activities. This person will be responsible for production, testing, and associated documentation is within industry guidelines.Responsibilities:* Assemble applicable documentation. * Process CAPAs and perform routine internal audits and maintain quality control.* Maintaining supplier files and audits.* Proper documentation of equipment. * Training new employees.* Develop quality system SOPs.* Inventory Products. * Follow (GMPs) and (SOPs).* Review and approve Analysis Certificates.* Print and approve product labels.Working hours: 8:00 AM - 5:00 PMSkills:*Plasmid purification and microbiology techniques. *Quality Assurance documentation.Education:BachelorsExperience:4-7 yearsQualifications:*GMP experience.*Bachelors degree in applicable life science field. 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
      • $32.00 - $33.00 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:Supervise manufacturing personnel through task assignment, delegation, and follow-up in production of plasmid DNA conforming to GMP guidelinesAssist in scaling-up processes to meet growing demands.Write Standard operating proceduresExecute validation protocolsPrepare solutions and materials required for the process.Follow batch records or SOPs to conduct cell banking, fermentation and purification processes for plasmid DNA manufacture at research or GLP scale.Conduct miniprep, concentration and gel analysis to in-process samples of research and cGMP productions.Install, commission and troubleshoot equipment as needed.Responsible for documentation and maintenance of equipment, such as: documenting new equipment and equipment changes, changing temperature charts, conducting and documenting PM for certain equipment, etc.Working hours: 6:00 AM - 3:00 PMSkills:Possess leadership skillsExcellent written and verbal communication skillsAbility to work in a clean room environment for extended periods of timeAbility to wear and work in PPEEducation:AssociateExperience:1-4 yearsQualifications:- Bachelors or Associates degree in a science related field with 3 or more years of cGMP manufacturing experience- Plasmid purification experience, preferred- Knowledge of Bio-processing, preferred Apply 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.
      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:Supervise manufacturing personnel through task assignment, delegation, and follow-up in production of plasmid DNA conforming to GMP guidelinesAssist in scaling-up processes to meet growing demands.Write Standard operating proceduresExecute validation protocolsPrepare solutions and materials required for the process.Follow batch records or SOPs to conduct cell banking, fermentation and purification processes for plasmid DNA manufacture at research or GLP scale.Conduct miniprep, concentration and gel analysis to in-process samples of research and cGMP productions.Install, commission and troubleshoot equipment as needed.Responsible for documentation and maintenance of equipment, such as: documenting new equipment and equipment changes, changing temperature charts, conducting and documenting PM for certain equipment, etc.Working hours: 6:00 AM - 3:00 PMSkills:Possess leadership skillsExcellent written and verbal communication skillsAbility to work in a clean room environment for extended periods of timeAbility to wear and work in PPEEducation:AssociateExperience:1-4 yearsQualifications:- Bachelors or Associates degree in a science related field with 3 or more years of cGMP manufacturing experience- Plasmid purification experience, preferred- Knowledge of Bio-processing, preferred Apply 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.
      • Spring, Texas
      • Temp to Perm
      • $20.00 - $24.00 per hour
      • 8:00 AM - 5:00 PM
      Spherion Staffing has partnered with a local bio-pharmaceutical industry leader to recruit for this role. This primary purpose of the Validation Specialist will be to support production and product quality. Verification and validation of equipment and documentation and products to ensure products are in accordance with company requirements.Responsibilities:* Support validation by developing validation documentation protocols and executing them.* Compiling data and authoring reports*Support new products, optimize processes, and technology transfers.*Support Quality Control and validate assays.*Support Quality Control instrumentation.* Participate in team projects in order to implement product development. * Maintain process and validation schedules and filing to company standards.* Training of staff and team growth support. * Stay current of all process technology and recommend improvements as needed. * Report to Quality Assurance manager status of Operations.Working hours: 8:00 AM - 5:00 PMSkills:* Validation and re-Validation of Quality Control assays preferred. * Qualification and re-Qualification of Quality Control testing and instrumentation preferred. * GMP experience. * Experience in Pharmaceutical and Biologics preferred.Education:BachelorsExperience:1-4 yearsQualifications:* 1 - 3 years applicable experience.* Bachelor's degree in Life Sciences field, or experience or training in a Pharmaceutical or Biologics environment. www.spherion.comSpherion 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 local bio-pharmaceutical industry leader to recruit for this role. This primary purpose of the Validation Specialist will be to support production and product quality. Verification and validation of equipment and documentation and products to ensure products are in accordance with company requirements.Responsibilities:* Support validation by developing validation documentation protocols and executing them.* Compiling data and authoring reports*Support new products, optimize processes, and technology transfers.*Support Quality Control and validate assays.*Support Quality Control instrumentation.* Participate in team projects in order to implement product development. * Maintain process and validation schedules and filing to company standards.* Training of staff and team growth support. * Stay current of all process technology and recommend improvements as needed. * Report to Quality Assurance manager status of Operations.Working hours: 8:00 AM - 5:00 PMSkills:* Validation and re-Validation of Quality Control assays preferred. * Qualification and re-Qualification of Quality Control testing and instrumentation preferred. * GMP experience. * Experience in Pharmaceutical and Biologics preferred.Education:BachelorsExperience:1-4 yearsQualifications:* 1 - 3 years applicable experience.* Bachelor's degree in Life Sciences field, or experience or training in a Pharmaceutical or Biologics environment. www.spherion.comSpherion 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 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.

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