Spherion has joined forces with a prominent biotechnology firm in College Station, TX to seek out skilled manufacturing technicians. These technicians will collaborate within teams specializing in upstream manufacturing, downstream manufacturing, or buffer preparation, utilizing diverse technological platforms. The primary responsibilities include executing manufacturing operations, adhering strictly to GMP regulations, and contributing to the production of vaccines and therapeutics.
Responsibilities:
Upstream Unit:
Single-Use Cell Culture Vessels/Bioreactors up to 2000L
Bacterial Fermentation Culture Vessels up to 2000L
Alpha Wasserman Continuous Flow Centrifuges
Disposable Magnetic Mixing Bags and Totes
Cell Expansion and Propagation
Banking/Cryopreservation of Cell Lines and Viruses
Hyperstack, Cellstack, and other Adherent Cell Technologies
Plate counting, microscopic examination
Monitor cultures, take samples, turn-around of bioreactor and fermenters, sterilization, and inoculation
Downstream Unit:
Medium to Large-scale filtration systems including Tangential Flow Filtration (TFF), Hollow FiberTangential Flow Filtration (HFTFF), Nanofiltration and depth filtration
Medium to Large-scale Chromatographic systems(AKTA).
Pre-Packed Columns from 1L to 100L
Single use mixing systems (Pall &GE)
Single Use connectivity types such as GE DAC and Colder AseptiQuik
Bulk filling
Aseptic process simulation and drug product filling
Plate counting, microscopic examination
Monitor cultures, take samples, turn-around of bioreactor and fermenters, sterilization, and inoculation
Buffer Preparation Unit:
Preparation of medium from stock raw materials including the compounding, mixing, testing and filtration for further process needs
Preparation of buffers from stock raw materials including the compounding, mixing, testing and filtration for further process needs
Weighing of raw materials per batch record specifications and assignment of appropriate expiry per procedures
Integrity testing of filters
Essential Functions Include:
Write and review standard operating procedures, buffer formulation records and batch production records.
Assist senior staff in implementing project safety and quality assurance programs in accordance with SOPs.
Maintain the confidentiality of proprietary company information.
Document and maintain activity records according to cGMP regulations and ensure junior team members are trained.
Operate general production equipment such as Autoclaves, Glass washers, Incubators, Analytical Scales, pH/conductivity meters, etc.
Perform daily cleaning and sanitization of the laboratory and manufacturing areas.
Maintain an effective working relationship with others.
Perform all other duties as assigned.
Working hours: 6:00 AM - 6:00 PM (Various Shifts Available)
Skills:
Experience in a GMP environment
Biotechnology Certificate
Education:
High School
Experience:
1-4 years
Qualifications:
Excellent oral and written communication skills, interpersonal and organizational skills.
Proficient with Microsoft Office applications.
Excellent leadership skills.
Ability to train others to perform to cGMP standards.
Good 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.
Excellent math and computer skills.
Experience working in a cleanroom environment with full clean room gowning and good aseptic technique.
Must have good planning and time management skills and be willing and able to interface with colleagues in many
different roles and functions throughout the manufacturing facilities.
Start a career in biotech!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. Whether you're looking for temporary, temp-to-perm or direct hire opportunities, no one works harder for you than Spherion.

Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

At Spherion, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact Callcenter@spherion.com.

Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc.In addition, Spherion offers a comprehensive benefits package, including health, and an incentive and recognition program (all benefits are based on eligibility).
key responsibilities
Upstream Unit:Single-Use Cell Culture Vessels/Bioreactors up to 2000LBacterial Fermentation Culture Vessels up to 2000LAlpha Wasserman Continuous Flow CentrifugesDisposable Magnetic Mixing Bags and TotesCell Expansion and PropagationBanking/Cryopreservation of Cell Lines and VirusesHyperstack, Cellstack, and other Adherent Cell TechnologiesPlate counting, microscopic examinationMonitor cultures, take samples, turn-around of bioreactor and fermenters, sterilization, and inoculationDownstream Unit:Medium to Large-scale filtration systems including Tangential Flow Filtration (TFF), Hollow FiberTangential Flow Filtration (HFTFF), Nanofiltration and depth filtrationMedium to Large-scale Chromatographic systems(AKTA).Pre-Packed Columns from 1L to 100LSingle use mixing systems (Pall &GE)Single Use connectivity types such as GE DAC and Colder AseptiQuikBulk fillingAseptic process simulation and drug product fillingPlate counting, microscopic examinationMonitor cultures, take samples, turn-around of bioreactor and fermenters, sterilization, and inoculationBuffer Preparation Unit:Preparation of medium from stock raw materials including the compounding, mixing, testing and filtration for further process needsPreparation of buffers from stock raw materials including the compounding, mixing, testing and filtration for further process needsWeighing of raw materials per batch record specifications and assignment of appropriate expiry per proceduresIntegrity testing of filtersEssential Functions Include:Write and review standard operating procedures, buffer formulation records and batch production records.Assist senior staff in implementing project safety and quality assurance programs in accordance with SOPs.Maintain the confidentiality of proprietary company information.Document and maintain activity records according to cGMP regulations and ensure junior team members are trained.Operate general production equipment such as Autoclaves, Glass washers, Incubators, Analytical Scales, pH/conductivity meters, etc.Perform daily cleaning and sanitization of the laboratory and manufacturing areas.Maintain an effective working relationship with others.Perform all other duties as assigned.
experience
1-4 years
skills
Experience in a GMP environment Biotechnology Certificate
qualifications
Excellent oral and written communication skills, interpersonal and organizational skills.Proficient with Microsoft Office applications.Excellent leadership skills.Ability to train others to perform to cGMP standards.Good 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.Excellent math and computer skills.Experience working in a cleanroom environment with full clean room gowning and good aseptic technique.Must have good planning and time management skills and be willing and able to interface with colleagues in manydifferent roles and functions throughout the manufacturing facilities.
education
High School