Core Technician I - Viral Therapeutics

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.

Requirements

• 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.
• Capable of operating and supporting troubleshooting of manufacturing equipment.
• Strong documentation skills and working knowledge of Microsoft Office applications.
• Effective communication skills and ability to work both independently and in a team-based environment.
• Ability to stand for extended periods and perform physically demanding gowning and cleanroom tasks.
• Bachelor's degree in Life Sciences preferred; Associate's degree or relevant experience also acceptable.
• About Lonza:
• Ready to shape the future of life sciences?

Benefits

Additional Information

Core Technician I - Viral Therapeutics Location: This is an on-site position located in Houston, TX. Available shift: Day shift, 7:00 AM - 7:30 PM on a rotating 12-hour schedule, including weekends, to support continuous manufacturing operations. The purpose of this role is to support the GMP production of viral therapeutics through aseptic processing, including cell culture, purification, formulation, and fill/finish activities. This position is also responsible for maintaining cleanroom environments, preparing buffers and components, and ensuring adherence to cGMP standards and documentation practices. What you will get: This is a competitive, hourly paid position. In addition, below you will find a comprehensive summary of the benefits package we offer: Performance-related bonus. Medical, dental and vision insurance. 401(k) matching plan. Life insurance, as well as short-term and long-term disability insurance. Employee assistance programs. Paid time off (PTO). Compensation for this role will be determined by the candidate's qualifications, skills, experience, and relevant knowledge.

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