biopharmaceutical manufacturing support technician.

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 has partnered with a local company in The Woodlands for a Downstream Process Technician.Responsibilities:Perform daily process activities in compliance with SOPsOperate downstream process equipment and operations in compliance with cGMP requirementsSupport quality investigations as neededPrepare equipment and solutions for processing Troubleshoot analytical methods as neededPrepare and submit samples for QC and other testingComplete and review production recordsCollaborate with QA when compliance issues ariseWorking hours: 8:00 AM - 5:00 PMSkills:Experience with chromatography and/or protein purification methods and design (preferred)Experience in a cGMP environment and implementation of continuous improvement practices (preferred)Broad understanding of general biology techniquesHands-on laboratory experience Ability to work various shiftsWillingness to work in The Woodlands and ConroeAbility to work independently and as part of a cross-functional teamAbility to multitask, understand goals, and set prioritiesStrong attention to detailEducation:BachelorsExperience:4-7 yearsQualifications:Bachelors in Biology, Molecular Biology, or other related disciplinesWilling to work in both The Woodlands and Conroe is necessaryExperience in Chromatography and or protein purification methods and designs is preferred 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 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.