Quality Control Analyst, Gene Therapy

United States, Houston (Texas)

Please note we are hiring for both 1st Shift and 2nd Shift openings.

Both shifts are scheduled for 4X10, that can either run Wednesday-Saturday, or Sunday-Wednesday. We have more openings for Wed-Sat.

Please ensure you can work this schedule prior to applying.

Today, Lonza is a global leader in life sciences operating across three continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of.

The Quality Control (QC) Analyst, Gene Therapy is responsible for Gene

Therapy product release and stability testing in support of the site contract manufacturing business.   Performs testing to Standard Operating Procedures and Test Methods in compliance with cGMP/GLP while working in a team atmosphere.

Key responsibilities:

  • Performs Gene Therapy product release and stability testing in support of the site contract manufacturing business according to Standard Operating Procedures and Test Methods in compliance with cGMP/GLP utilizing proper aseptic techniques (where applicable).
  • Participate in QC testing of clinical and commercial grade product according to cGMPs.
  • Perform cell-mediated bioassays, including infectious and physical titer, Western blot, (enzyme-linked immunosorbent assay) ELISA, (polymerase chain reactionqPCR, (high-performance liquid chromatography) HPLC, (ultraviolet–visible spectroscopy) UV-Vis.
  • Execute qualification or validation of test methods
  • Prepare samples and maintain appropriate records for submission of samples to contract testing laboratories. Ship samples to contract labs.
  • Communicates with subcontract labs to obtain information regarding capabilities, test timelines, and costs for testing unable to be performed in-house.  Prepares sample shipments and submission paperwork for contract laboratory testing. 
  • May initiate and assist with (out of specification) OOS/deviation investigations.
  • May write and revise Standard Operating Procedures (SOPs). 
  • Performs general lab support activities such as housekeeping, equipment maintenance, inventory/ordering of supplies. 
  • Maintains compliance with all required training.

Key requirements:

  • Bachelor’s degree in Sciences, Master’s degree highly preferred. 
  • xperience with cell-based assay testing such as physical and infectious titer, (polyacrylamide gel electrophoresis) SDS-PAGE, Western Blot, ELISA, HPLC, UV-Vis, microbiological testing
  • Advanced knowledge of cGMP policies and procedures. 
  • Exposure to viral vector or virology is desired.  
  • Acquires and documents training on all laboratory general tasks and can perform assigned test methods and using associated instrumentation.
  • Understanding of basic laboratory equipment and aseptic technique a plus.
  • Proficient in the use of spreadsheets, databases, and word processing software.
  • Problem solves by selecting appropriate alternative from defined options.
  • Ability to communicate and write effectively.
  • Dependable and able to work well within a team.

Every day, Lonza’s products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.

People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.

Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.

Reference: R31768
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