CLEAN ROOM TECHNICIAN

Spherion; College Station (TX); On-site; USD 52,000 - 75,000; Full time

Benefits offered by this job

Medical, dental, vision, life

401(k) plan

Short-term disability

Job summary

Spherion Staffing, LLC is seeking a detail-oriented Clean Room Technician to support ISO-classified manufacturing suites for biopharmaceutical production in Texas. You will perform decontamination, disinfection, and environmental monitoring of sterile areas, aiding in the production of cell and gene therapies.

Responsibilities include cleaning ISO suites, adhering to PPE requirements, maintaining GDP/cGMP records, and safely handling waste.

Qualifications

• 1-4 years of experience in a cGMP environment.
• Associate's or Bachelor's degree in a scientific or technical field.
• Familiarity with aseptic techniques and ISO 14644 standards.
• Experience using Quality Management Systems (QMS) or electronic batch records.
• Ability to troubleshoot basic equipment malfunctions and identify opportunities for process improvement.

Responsibilities

• Clean ISO 5/7/8 suites daily and periodically.
• Follow gowning PPE and aseptic practices.
• Maintain GDP/cGMP records in logbooks and digital systems.
• Dispose of biohazardous and chemical waste per regs.
• Support monitoring equipment setup for air quality and surface microbial levels.
• Operate autoclaves, VHP systems, and filtration tools.
• Assist with audits and report SOP deviations.

Skills

cGMP experience

Science degree

Aseptic techniques

QMS familiarity

Troubleshooting

Education

Associate's or Bachelor's degree

Job description

We are seeking a detail-oriented and disciplined Clean Room Technician to join a manufacturing team. In this role, you will be a critical guardian of our controlled environments, ensuring that our ISO-classified manufacturing suites meet the rigorous cleanliness and safety standards required for advanced biopharmaceutical production. You will be responsible for the decontamination, disinfection, and environmental monitoring of sterile areas, directly supporting the production of life-changing cell and gene therapies.

Responsibilities

• Perform daily and periodic cleaning, decontamination, and disinfection of ISO 5, ISO 7, and ISO 8 cleanroom suites, including ceilings, walls, floors, and equipment.
• Adhere strictly to gowning (PPE) requirements and aseptic behaviors to prevent the introduction of particles or microbes into controlled environments.
• Maintain accurate, real-time records in logbooks and electronic systems according to Good Documentation Practices (GDP) and current Good Manufacturing Practices (cGMP).
• Safely remove and dispose of biohazardous and chemical waste in accordance with safety procedures and environmental regulations.
• Assist with the setup and operation of monitoring equipment to track air quality, pressure differentials, and surface microbial levels.
• Operate and maintain cleaning equipment such as autoclaves, vaporized hydrogen peroxide (VHP) systems, and specialized filtration tools.
• Participate in audit readiness initiatives and immediately report any facility deficiencies or deviations from Standard Operating Procedures (SOPs).

Working hours

8:00 AM - 5:00 PM

Skills

• 1-2 years of experience in a cGMP environment (biotech, pharmaceutical, or medical device manufacturing).
• Associate's or Bachelor's degree in a scientific or technical field.
• Familiarity with aseptic techniques, ISO 14644 standards, or cleanroom gowning procedures.
• Experience using Quality Management Systems (QMS) or electronic batch records.
• Ability to troubleshoot basic equipment malfunctions and identify opportunities for process improvement.

Education

High School

Experience

1-4 years

Qualifications

• Ability to follow complex, multi-step instructions (SOPs) with 100% accuracy.
• Ability to stand for extended periods and lift up to 40 lbs.
• Strong track record of attendance and punctuality in a shift-based environment.
• Effective verbal and written communication skills for reporting and team coordination.
• High School Diploma or GED.

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 [e-mail].

Pay and Benefits

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.

• medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility).

Key Responsibilities

• Perform daily and periodic cleaning, decontamination, and disinfection of ISO 5, ISO 7, and ISO 8 cleanroom suites, including ceilings, walls, floors, and equipment.
• Adhere strictly to gowning (PPE) requirements and aseptic behaviors to prevent the introduction of particles or microbes into controlled environments.
• Maintain accurate, real-time records in logbooks and electronic systems according to Good Documentation Practices (GDP) and current Good Manufacturing Practices (cGMP).
• Safely remove and dispose of biohazardous and chemical waste in accordance with safety procedures and environmental regulations.
• Assist with the setup and operation of monitoring equipment to track air quality, pressure differentials, and surface microbial levels.
• Operate and maintain cleaning equipment such as autoclaves, vaporized hydrogen peroxide (VHP) systems, and specialized filtration tools.
• Participate in audit readiness initiatives and immediately report any facility deficiencies or deviations from Standard Operating Procedures (SOPs).

Experience

1-4 years

Skills

• 1-2 years of experience in a cGMP environment (biotech, pharmaceutical, or medical device manufacturing).
• Associate's or Bachelor's degree in a scientific or technical field.
• Familiarity with aseptic techniques, ISO 14644 standards, or cleanroom gowning procedures.
• Experience using Quality Management Systems (QMS) or electronic batch records.
• Ability to troubleshoot basic equipment malfunctions and identify opportunities for process improvement.

Qualifications

• Ability to follow complex, multi-step instructions (SOPs) with 100% accuracy.
• Ability to stand for extended periods and lift up to 40 lbs.
• Strong track record of attendance and punctuality in a shift-based environment.
• Effective verbal and written communication skills for reporting and team coordination.
• High School Diploma or GED.

Education

High School