Core Technician – Cell Therapy Overnight

Lonza Group; Houston (TX); On-site; USD 34,000 - 55,000; 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 is seeking a Core Technician – Cell Therapy Overnight in Houston, TX to support aseptic processing and manufacturing of cell therapy products within a GMP environment. You will operate production equipment and complete GMP docs as part of a cross-functional team.

Ideal candidates have 1–2 years of related experience, strong knowledge of aseptic techniques, and the ability to read SOPs and production schedules. This on-site role offers an hourly pay and comprehensive benefits.

Qualifications

• High school diploma or equivalent required; associate degree preferred.
• 1–2 years of experience with cell therapy technologies in a cGMP environment.
• Knowledge of aseptic processing principles and cleanroom operations.
• Ability to read, understand and follow SOPs and production schedules.
• Understanding of cGMP and regulatory compliance.
• Experience completing GMP documentation and reviewing manufacturing records preferred.
• Proficiency with Microsoft Excel; SAP and LIMS desirable.
• Strong organizational, time management and prioritization skills.
• Effective verbal and written communication; collaborative teamwork.
• Self-motivated and committed to operational excellence.
• Ability to perform aseptic gowning regularly; stand up to 6 hours; lift up to 50 pounds.

Responsibilities

• Participate in aseptic processing and manufacture of clinical and commercial cell therapy products.
• Perform aseptic cell culture manipulations in Grade A/B cleanroom.
• Operate cell processing and manufacturing equipment per SOPs.
• Troubleshoot basic equipment issues and escalation as needed.
• Follow contamination control and containment strategies in GMP environment.
• Participate in assigned APS (Aseptic Process Simulations).
• Complete GMP documentation accurately and timely.
• Review manufacturing batch records and related GMP docs.
• Adhere to safety policies and applicable regulations.
• Document deviations from procedures and support investigations.
• Follow production schedules and execute manufacturing activities efficiently.
• Collaborate with Manufacturing, QA, QC and other site functions.
• Perform additional duties to support operations.

Skills

Cell therapy technologies experience

SOP reading & execution

Microsoft Excel proficiency

Team collaboration

Education

High school diploma or equivalent

Associate degree in scientific/technical discipline preferred

Tools

SAP

LIMS

Job description

Core Technician – Cell Therapy Overnight

United States, Houston (Texas)

Core Technician – Cell Therapy Overnight

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

As a Core Technician - Cell Therapy Overnight, 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 escape 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.

Why Lonza:

We are a place of unique opportunity, where your ideas, expertise and ambition can make a real difference. Here, will have the freedom to grow, the support to succeed and the chance to contribute to work that matters.

We are the makers of the medicines of tomorrow.