United States, Houston (Texas)
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.
Are you looking to join a team where your efforts will make a world-class impact? Lonza AG is growing, and we are on the lookout for a dedicated Health Care professional to join our ambitious team in Houston, TX. As part of our innovative biopharmaceutical production team, you’ll be integral to advancing life-saving treatments and therapies.

Key responsibilities:

• Operate cell culture bioreactors with precision.
• Perform large-scale purification by ion exchange chromatography.
• Complete aseptic filling procedures flawlessly.
• Conduct cGMP training for both new and current employees.
• Participate in internal and external audits as required.
• Review and maintain cGMP records, ensuring compliance.
• Implement change control processes successfully.
• Stock cleanroom suites and support areas with released inventory.
• Maintain the cleanroom environment at flawless standards by strictly following established cleaning practices.
• Package kits, blood tubes, and final product for shipment.
• Monitor expiry dates of critical raw materials meticulously.
• Align with processes, procedures, and instructions for all activities.
• Perform procedures according to written guidelines and recognize deviations from accepted practice.

Key requirements:

• Proven experience in a GMP facility.
• Outstanding knowledge of cell culture bioreactor operations.
• Expertise in ion exchange chromatography.
• Strong understanding of aseptic filling techniques.
• Ability to train staff on cGMP processes.
• Experience with internal and external audits.
• Proficiency in reviewing and maintaining cGMP records.
• Ability to manage inventory and maintain cleanroom standards.
• Meticulous attention to detail in monitoring raw material expiry dates.
• Strict adherence to established procedures and recognition of deviations.
• Willingness to work days and weekends on a 12-hour shift rotation.

Join us at Lonza AG, where your work will contribute to our mission of improving lives worldwide. now to be part of a dynamic team dedicated to outstanding scientific solutions!
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: R68310

• Operate cell culture bioreactors with precision.
• Perform large-scale purification by ion exchange chromatography.
• Complete aseptic filling procedures flawlessly.
• Conduct cGMP training for both new and current employees.
• Participate in internal and external audits as required.
• Review and maintain cGMP records, ensuring compliance.
• Implement change control processes successfully.
• Stock cleanroom suites and support areas with released inventory.
• Maintain the cleanroom environment at flawless standards by strictly following established cleaning practices.
• Package kits, blood tubes, and final product for shipment.
• Monitor expiry dates of critical raw materials meticulously.
• Align with processes, procedures, and instructions for all activities.
• Perform procedures according to written guidelines and recognize deviations from accepted practice