Environmental Monitoring Core Technician

Environmental Monitoring Core Technician

Based in Houston, TX. As an Environmental Monitoring Technician, you will perform critical monitoring activities to maintain cleanroom readiness and support aseptic processing operations. This is an exciting opportunity for a laboratory professional to help deliver clinical-grade therapies while building a career in biotech.

Fully site‑based roles: 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:

• Perform environmental monitoring activities in support of GMP manufacturing and aseptic processing operations.

• Operate environmental monitoring equipment, including air samplers, particle counters, and related monitoring systems.

• Prepare buffers, components, and materials required for manufacturing activities, including operation of autoclave equipment.

• Maintain, stock, and set up cleanroom environments to support production readiness.

• Complete, review, and update manufacturing documentation, batch records, and environmental monitoring records accurately and compliantly.

• Coordinate environmental monitoring equipment and sampling requirements with Quality Control partners.

• Support routine clinical production activities through the operation of manual, semi-automated, and automated equipment while adhering to GMP requirements.

What we are looking for:

• Bachelor's degree in Life Sciences preferred, or equivalent combination of education and relevant experience.

• 1–3 years of laboratory, manufacturing, or biopharmaceutical industry experience.

• Experience working in a GMP-regulated environment is preferred.

• Knowledge of aseptic techniques, cleanroom practices, or environmental monitoring activities is advantageous.

• Strong attention to detail with the ability to follow procedures and maintain accurate documentation.

• Ability to work independently and collaboratively in a team-oriented environment.

• Willingness and ability to work a rotating 12-hour day shift schedule and complete initial training on first shift.

About Lonza

At Lonza, their people are their greatest strength. With 30+ sites across five continents, their globally connected teams work together every day to manufacture the medicines of tomorrow. Their core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who they are and how they work together. Everyone’s ideas, big or small, have the potential to improve millions of lives, and that’s the kind of work they want you to be part of.

Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, they value diversity and are committed to creating an inclusive environment.

As Lonza’s talent acquisition partner, please note, Randstad is responsible for the engagement and contracting of this contingent role.

Ready to play your part in shaping the future of life sciences? Apply now.