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      • 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.
      • Spring, Texas
      • Temp to Perm
      • $20.00 - $23.00 per hour
      • 8:00 AM - 5:00 PM
      The primary purpose of the Production Planner is to coordinate production for multiple planned projects and products. The Production Planner will be responsible for planning and prioritization of applicable operations and meeting deadlines.Responsibilities:* Coordinate workflows* Ensure production performance and monitor production performance in a timely manner. * Determine production materials needed.* Approve manufacturing orders.* Utilize ERP software to set up items and Bill of Material.* Problem resolution and determination of priorities. *Communicate support functions. * Ensure proper inventory levels. * Document status and performance reports. * Author SOPs and compose reports.* Inventory counts.Working hours: 8:00 AM - 5:00 PMSkills:* Microsoft Suites* Professional verbal and writing skills.* Understanding of Manufacturing processes and time management. * Supply chain experience with ERP software.* Experience with Oracle, NetSuite preferred.Education:High SchoolExperience:1-4 yearsQualifications:* GMP experience.* High School Diploma or GED* 3 - 5 years Production Planning or Pharmaceuticals Manufacturing environment experience. 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.
      The primary purpose of the Production Planner is to coordinate production for multiple planned projects and products. The Production Planner will be responsible for planning and prioritization of applicable operations and meeting deadlines.Responsibilities:* Coordinate workflows* Ensure production performance and monitor production performance in a timely manner. * Determine production materials needed.* Approve manufacturing orders.* Utilize ERP software to set up items and Bill of Material.* Problem resolution and determination of priorities. *Communicate support functions. * Ensure proper inventory levels. * Document status and performance reports. * Author SOPs and compose reports.* Inventory counts.Working hours: 8:00 AM - 5:00 PMSkills:* Microsoft Suites* Professional verbal and writing skills.* Understanding of Manufacturing processes and time management. * Supply chain experience with ERP software.* Experience with Oracle, NetSuite preferred.Education:High SchoolExperience:1-4 yearsQualifications:* GMP experience.* High School Diploma or GED* 3 - 5 years Production Planning or Pharmaceuticals Manufacturing environment experience. 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
      • $20.00 - $23.00 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 review documentation of the Process Development team to ensure compliance with regulatory requirements.Responsibilities:* Review for compliance and approve all documentation for Research Grade and Highly Documented products.* Write up deviations and investigations.* Write and review all SOPs for Process Development team.* Review records related to production and process development. * Follow GMPs and SOPs to ensure company compliance. * Maintain applicable product inventories.* Summarize data.* Write Plasmid DNA evaluation summaries.Working hours: 8:00 AM - 5:00 PMSkills:* Must have previous technical writing experience in a lab setting.* Experience working in a GMP facility or pharmaceutical environment.* Experience with GMPs and SOPs as applicable to manufacture of Plasmid DNA* Technical writing and reviewing abilities. * Attention to detail and commitment to compliance.* Ability to identify and document scientific deviations.* Inventory maintenance.Education:AssociateExperience:1-4 yearsQualifications:* Associates degree.* Between 1 - 3 years experience in related role. 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 review documentation of the Process Development team to ensure compliance with regulatory requirements.Responsibilities:* Review for compliance and approve all documentation for Research Grade and Highly Documented products.* Write up deviations and investigations.* Write and review all SOPs for Process Development team.* Review records related to production and process development. * Follow GMPs and SOPs to ensure company compliance. * Maintain applicable product inventories.* Summarize data.* Write Plasmid DNA evaluation summaries.Working hours: 8:00 AM - 5:00 PMSkills:* Must have previous technical writing experience in a lab setting.* Experience working in a GMP facility or pharmaceutical environment.* Experience with GMPs and SOPs as applicable to manufacture of Plasmid DNA* Technical writing and reviewing abilities. * Attention to detail and commitment to compliance.* Ability to identify and document scientific deviations.* Inventory maintenance.Education:AssociateExperience:1-4 yearsQualifications:* Associates degree.* Between 1 - 3 years experience in related role. 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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