Core Technician I

Lonza; Houston (TX); On-site; Confidential; Full time

Benefits offered by this job

Performance-related bonus

Medical, dental and vision insurance

401(k) matching plan

Life insurance, disability coverage

Employee assistance programs

Paid time off (PTO)

Job summary

Lonza in Houston, TX is seeking a Core Technician I to support GMP production of viral therapeutics on a day shift in a rotating 12-hour schedule. You will work in aseptic processing, cell culture, purification, formulation, and fill/finish activities, maintaining cleanroom operations and strict cGMP documentation.

The role requires following SOPs precisely under supervision, with strong focus on accuracy and teamwork.

Qualifications

• Bachelor's degree in Life Sciences preferred; associate degree or relevant experience acceptable.
• Experience with aseptic techniques and cGMP environments required.
• Ability to follow SOPs with accuracy under supervision.
• Strong documentation skills and cleanroom familiarity.

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

Gowning procedures

Troubleshooting

Teamwork

Microsoft Office

Education

Bachelor's degree in Life Sciences

Associate degree or relevant experience

Tools

Autoclaves

Process equipment

Job description

Core Technician I

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.

This is a competitive, hourly paid position.

What you will get:

• 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.

What you will do:

• 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.

What we are looking for:

• 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:

At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone's ideas, big or small, have the potential to improve millions of lives, and that's the kind of work we want you to be part of.

Innovation thrives when people from all backgrounds bring their unique perspectives to the table.

At Lonza, we offer equal employment opportunities to all qualified applicants regardless of race, religion, color, national origin, sex, sexual orientation, gender identity, age, disability, veteran status, or any other characteristic protected by law.

If you're ready to help turn our customers' breakthrough ideas into viable therapies, we look forward to welcoming you on board.