Material Handler II (Day Shift)

Material Handler II

Based in Houston, TX, you will join our Production Support team to manage critical supply chain operations and goods movement. By ensuring materials are accurately tracked, prepared, and delivered, you will directly support the seamless manufacture of life-changing therapies within a highly regulated cGMP environment.

This is a fully site‑based role. Working together in person supports close, real‑time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards.

What you will get:

• An agile career and dynamic working culture.

• An inclusive and ethical workplace.

• Competitive hourly rate.

What you will do:

• Manage and maintain critical stock levels, ensuring production teams have the daily supplies required for seamless operations.

• Operate GMP Autoclave equipment to safely prepare and sterilize supplies and documents needed for active production.

• Execute physical material transfers and decontamination processes, carefully managing the flow of materials from controlled non-classified (CNC) spaces into classified production suites.

• Perform and accurately record a variety of material movement transactions in SAP, strictly adhering to Good Documentation Practices (GDP) and SOPs.

• 2- 3- 2 schedule after training. 12 hour shifts

• Complete cross-training on specialized operational equipment to broaden your understanding of the site's complete supply chain lifecycle.

What we are looking for:

• A High School Diploma or equivalent.

• Prior hands-on experience working in a clean room environment and operating autoclaving equipment is highly preferred.

• Previous exposure to SAP system transactions for tracking inventory and material movements is strongly preferred.

• Familiarity with cGMP (Current Good Manufacturing Practice) environments and a strong understanding of regulatory documentation standards.

• Strong organizational and time-management skills, with the ability to prioritize tasks and meet critical production deadlines.

• A collaborative team player with clear verbal and written communication skills, plus basic proficiency in Microsoft Office Suite.

About Lonza

Founded in 1897 in the Swiss Alps, our business has embraced innovation and kept pace with a fast-changing world for more than 125 years.

We are the CDMO that opened the door to a new era of medicine – one where breakthroughs could be produced at scale and made available around the world. Our contributions have led the way in drug approvals in our industry.

The therapies we help bring to life reach up to 100 million people each year, and we contribute to around one in every ten medicines that are newly approved by the FDA.

Political, regulatory, or economic disruption in one region doesn’t put the brakes on our business as our global network of 30+ sites across five continents provides resilience against global instability.

We are a community of big thinkers and bold doers. We focus on what matters, and together we make it happen. We are constantly pushing ourselves to make things better, never stopping until we make it right.

Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, national origin, age, disability, protected veteran status, genetic information, or any other characteristic protected by applicable federal, state, or local law.

At Lonza, we are committed to building an inclusive workplace where diverse perspectives are valued and respected. We believe that diversity strengthens our teams, drives innovation, and helps us better serve our employees, customers, and communities. Reasonable accommodations are available for qualified individuals with disabilities throughout the recruitment process.