GMP Viral Production Technician (12h Shifts)

Lonza Group; Houston (TX); On-site; USD 30,000 - 41,000; Full time

Benefits offered by this job

Performance-related bonus

Medical, dental, and vision insurance

401(k) matching plan

Life insurance and disability cover

Employee assistance programs

Paid time off (PTO)

Job summary

Lonza is seeking a hands-on GMP production teammate to support viral therapeutics manufacturing in a Houston-area facility. You will perform aseptic processing, large-scale cell culture, and downstream activities while maintaining strict cGMP documentation and cleanroom standards.

The role involves preparing buffers, operating autoclaves, and supporting validation and troubleshooting within a fast-paced, safety-conscious environment.

Qualifications

• Demonstrated knowledge of aseptic techniques and cGMP manufacturing environments required.
• Experience with cell culture, viral production, or related bioprocessing techniques preferred.
• Ability to follow detailed SOPs and perform tasks under close supervision while maintaining accuracy and compliance.
• Familiarity with cleanroom operations, including gowning qualifications and behavior standards.

Responsibilities

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

Skills

Aseptic techniques

cGMP manufacturing

Cell culture

Documentation

SOP adherence

Teamwork

Microsoft Office

Troubleshooting

Education

Bachelor’s degree in Life Sciences

Associate’s degree or relevant experience

Tools

Autoclaves

Job description

Lonza is seeking a hands-on GMP production teammate to support viral therapeutics manufacturing in a Houston-area facility. You will perform aseptic processing, large-scale cell culture, and downstream activities while maintaining strict cGMP documentation and cleanroom standards.

The role involves preparing buffers, operating autoclaves, and supporting validation and troubleshooting within a fast-paced, safety-conscious environment.