Core Technician - Viral Vector Night Shift

Lonza Biologics Porriño SLU; Houston (TX); On-site; USD 50,000 - 75,000; Full time

Job summary

Join a leading global life sciences company as a Core Technician - Viral Vector on the night shift. You'll play a critical role in aseptic processing, bioreactor operation, and compliance in a GMP environment, contributing to the improvement of biopharmaceuticals. Leverage your technical skills and detail-oriented mindset in an innovative and mission-driven setting while making a meaningful impact.

Qualifications

• Experience in a GMP facility (0-4 years).
• Proven knowledge of aseptic processing.
• Ability to train and motivate team members.

Responsibilities

• Perform aseptic processing of clinical-grade products.
• Operate cell culture bioreactors and conduct purification.
• Complete aseptic filling processes and maintain a sterile environment.

Skills

Technical Skills

Attention to Detail

Troubleshooting

Collaboration

Education

Bachelor or Associate's Degree in Life Sciences

Job description

Core Technician - Viral Vector Night Shift

United States, Houston (Texas)

Today, Lonza is a global leader in life sciences operating across five 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.

Join our team as a Core Tech II – Viral Vector (Night Shift) and help shape the future of biopharmaceuticals. In this GMP-regulated role, you'll operate bioreactors, perform large-scale purification, support aseptic filling, and contribute to cGMP training and compliance. We're seeking detail-oriented professionals with strong technical skills and a passion for quality. Apply now to grow your career in a purpose-driven, innovative environment.

We’re looking for someone who brings technical know-how, attention to detail, and a commitment to quality. If you're ready to grow your career in an innovative and mission-driven environment, we want to hear from you!

Apply today and be a part of something bigger where science meets purpose.

Key responsibilities:

Perform aseptic processing of clinical-grade products, including cell culture, purification, formulation, and filling activities according to approved production records and cGMPs.

Operate cell culture bioreactors and conduct large-scale purification by ion exchange chromatography.

Complete aseptic filling processes and maintain a sterile environment.

Investigate and troubleshoot deviations and unexpected events to ensure seamless operations.

Review, write, and complete production records meticulously.

Conduct cGMP training for new and current employees, encouraging a knowledgeable and compliant team.

Support the maintenance of cleanroom environments by following established cleaning practices and stocking cleanroom suites.

Perform environmental monitoring and ensure the timely completion of product batches.

Monitor the expiry of critical raw materials and maintain accurate records.

Key requirements:

Bachelor or associate's degree in Life Sciences experience 0-4 years.

Willingness to work Nights, and Weekends. Shift: 7:00 AM – 7:30 PM (rotating 2-2-3 schedule)

Proven experience in a GMP facility with a focus on cell culture and purification processes.

Strong knowledge of aseptic processing and cGMP compliance.

Excellent troubleshooting skills and the ability to effectively investigate deviations.

Ability to perform procedures according to written guidelines and recognize deviations.

Experience in conducting training and maintaining a positive work climate.

Capable of motivating others, setting clear objectives, and handling competing priorities.

Comfortable working in a cleanroom environment with required protective gear.

Strong dedication to safety policies, rules, and regulations.

Outstanding ability to collaborate and communicate effectively across departments.

Join us at Lonza AG, where your expertise will help us compete at the highest level and make a significant impact on the world. Apply now to be a part of something outstanding!

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.