GMP Aseptic Technician – Viral Therapeutics (Houston)

Lonza Group; Houston (TX); On-site; USD 30,000 - 47,000; Full time

Benefits offered by this job

Performance-related bonus

Medical, dental and vision insurance

401(k) matching plan

Life insurance

Short-term and long-term disability

Employee assistance programs

Paid time off

Job summary

Lonza in Houston is seeking a GMP production technician to support viral therapeutics manufacturing. This on-site role involves aseptic processing, cell culture, purification, formulation, and fill/finish operations within a cleanroom environment.

You will operate autoclaves and process equipment, maintain rigorous documentation, and ensure strict cGMP compliance. The role includes a rotating 12-hour schedule, weekends, and competitive hourly pay with comprehensive benefits.

Qualifications

• Aseptic techniques knowledge required.
• Experience in cGMP manufacturing environments preferred.
• Strong documentation and record-keeping skills.
• Proficiency with Microsoft Office applications.
• Ability to work independently and in a team.
• Bachelor’s in Life Sciences preferred; equivalent experience accepted.

Responsibilities

• Perform GMP-compliant production of viral therapeutic products, including large-scale mammalian cell culture.
• Execute aseptic processing across purification, formulation, and fill/finish.
• Prepare buffers and components and operate autoclaves and process systems.
• Operate manual, semi-automated, and automated production equipment for clinical manufacturing.
• Maintain cleanroom operations, stocking, setup, and gowning procedures.
• Assist in validation activities, equipment troubleshooting, changeovers, and data collection.
• Support cell banking activities and ensure accurate task documentation.

Skills

Aseptic techniques

cGMP manufacturing

Documentation

MS Office

Team collaboration

Independent work

Education

Bachelor’s degree in Life Sciences

Associate’s degree or relevant experience

Job description

Lonza in Houston is seeking a GMP production technician to support viral therapeutics manufacturing. This on-site role involves aseptic processing, cell culture, purification, formulation, and fill/finish operations within a cleanroom environment.

You will operate autoclaves and process equipment, maintain rigorous documentation, and ensure strict cGMP compliance. The role includes a rotating 12-hour schedule, weekends, and competitive hourly pay with comprehensive benefits.