Quality Control Analyst I - Cell Therapy (AM Shift)

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

Available shift: Sunday - Wednesday, 6:00 AM - 4:30 PM.

The Quality Control Analyst I - Cell Therapy (AM Shift) is responsible for performing Quality Control assays in support of the release and stability testing of cell therapy products. This position supports clinical and commercial manufacturing programs by executing biological and cell-based assays, maintaining accurate laboratory documentation, and ensuring compliance with cGMP regulations and quality standards. The role offers exposure to a diverse range of analytical techniques within a dynamic Cell Therapy Quality Control environment.

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:

• Perform Quality Control (QC) biological and cell-based testing of Cell Therapy release and stability samples. Typical assay methods include flow cytometry, ELISA, proliferation assays, manual and automated cell counting, and immunofluorescence-based testing.
• Execute testing activities in accordance with cGMP requirements and approved laboratory procedures.
• Maintain complete, accurate, and compliant laboratory documentation, including recording test results and maintaining raw data.
• Support Cell Therapy technology transfer activities and analytical method validation projects.
• Participate in training activities related to new methodologies, instrumentation, and procedures.
• Assist with the generation and maintenance of standard operating procedures (SOPs) and validation documentation.
• Perform routine laboratory and equipment maintenance activities to ensure operational readiness.
• Collaborate with Quality Assurance, Operations, and Supply Chain teams to support manufacturing and product release activities.
• Support investigations, deviations, and other quality documentation as required.
• Perform additional duties as assigned in support of Cell Therapy Quality Control operations.

What we are looking for:

• Bachelor's degree in Life Sciences or a related scientific discipline required.
• Experience working in a scientific laboratory environment preferred.
• Exposure to cGMP environments and regulated laboratory practices is a plus.
• Hands-on experience with Flow Cytometry, qPCR, Cell Counting, ELISA, or related analytical techniques is highly desirable.
• Demonstrated knowledge of biological and cell-based assays, including flow cytometry, preferred.
• Understanding of laboratory equipment, aseptic techniques, and sample handling practices preferred.
• Ability to follow procedures, operate laboratory instrumentation, and maintain accurate records.
• Strong attention to detail, organizational skills, and commitment to quality.
• Positive attitude, willingness to learn, and ability to work effectively in a team environment.

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.

Ready to shape the future of life sciences? Apply now.