Core Technician– Cell Therapy 3rd Shift

Lonza; Houston, Northern (TX, KY); Hybrid; Confidential; Full time

Benefits offered by this job

Performance-related bonus

Medical, dental and vision insurance

401(k) matching plan

Life insurance and disability coverage

Employee assistance programs

Paid time off

Job summary

Lonza is seeking a Core Technician - Cell Therapy in Houston to perform aseptic processing and cell culture activities within a GMP environment. You will operate production equipment, complete GMP documentation, and support manufacturing of clinical and commercial cell therapy products.

The role requires 1–2 years of related experience, a high school diploma (Associate degree preferred), and the ability to work on-site in Houston, TX. Competitive hourly pay and comprehensive benefits are offered.

Qualifications

• Experience in aseptic processing in a cGMP environment preferred.
• Ability to read, understand, and follow SOPs and production schedules.
• Proficiency with Microsoft Office applications, especially Excel; SAP and LIMS experience desirable.

Responsibilities

• Participate in aseptic processing and manufacture of cell therapy products.
• Perform aseptic manipulations in Grade A/B cleanrooms.
• Operate production equipment per approved SOPs and batch records.
• Troubleshoot basic equipment and escalate issues as needed.
• Follow GMP and contamination control procedures in manufacturing.
• Complete GMP documentation accurately and timely.
• Review batch records and related GMP docs as required.
• Collaborate with Manufacturing, QA, QC and other site functions.

Skills

Aseptic processing

Cell culture

SOP compliance

GMP understanding

Excel

Team collaboration

Education

High school diploma or equivalent

Associate degree in scientific/technical field preferred

Tools

SAP

LIMS

Job description

Location: This is an on-site position located in Houston, TX.

As a Core Technician - Cell Therapy, you will play a critical role in the manufacturing of clinical and commercial cell therapy products within a highly regulated GMP environment. This position is responsible for performing aseptic cell processing activities, operating production equipment, completing GMP documentation, and supporting the safe and compliant manufacture of life‑saving therapies. Working closely with Manufacturing, Quality, and Operational teams, you will help ensure products are produced according to established procedures, quality standards, and production schedules.

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.

What you will do:

• Participate in the aseptic processing and manufacture of clinical and commercial cell therapy products.
• Perform aseptic cell culture manipulations within Grade A/B cleanroom environments.
• Operate cell processing and manufacturing equipment according to approved SOPs.
• Troubleshoot basic equipment issues and elevate concerns as appropriate.
• Follow contamination control and containment strategies to maintain a compliant GMP manufacturing environment.
• Participate in assigned customer Aseptic Process Simulations (APS).
• Complete GMP documentation accurately, thoroughly, and in a timely manner.
• Review manufacturing batch records (MBRs) and related GMP documentation as required.
• Adhere to all safety policies, procedures, and applicable regulations.
• Identify, document, and communicate deviations from standard procedures and accepted practices.
• Provide accurate information and support during process deviation investigations.
• Follow production schedules and execute assigned manufacturing activities efficiently.
• Collaborate effectively with Manufacturing, Quality Assurance, Quality Control, and other site functions to support operational objectives.
• Perform additional duties as assigned in support of manufacturing operations.

What we are looking for:

• High school diploma or equivalent required; Associate degree in a scientific or technical discipline preferred.
• 1-2 years of experience working with cell therapy technologies or related biopharmaceutical manufacturing processes in a cGMP environment.
• Working knowledge of aseptic processing principles and cleanroom operations.
• Ability to perform aseptic manipulations while maintaining product and environmental integrity.
• Ability to read, understand, and follow SOPs, manufacturing instructions, and production schedules.
• Understanding of cGMP requirements and the importance of regulatory compliance.
• Experience completing GMP documentation and reviewing manufacturing records is preferred.
• Proficiency with Microsoft Office applications, including Excel; experience with SAP and LIMS is desirable.
• Strong organizational, time management, and prioritization skills.
• Effective verbal and written communication skills.
• Ability to work collaboratively within a team environment and resolve issues professionally.
• Self‑motivated, solution‑oriented, and committed to operational excellence.
• Ability to perform aseptic gowning on a routine basis.
• Ability to stand for extended periods, up to 6 hours.
• Ability to routinely lift up to 50 pounds.

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,Passionand Integrity reflect who we are and how we work together. Everyone’s ideas, big or small, have the potential to improve millions of lives, andthat’sthe 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. Ifyou’reready to help turn our customers’ breakthrough ideas intoviabletherapies, we look forward to welcoming you on board.