Quality Control Analyst II - Environmental Monitoring

Lonza•Houston, TX

1d•Onsite

About The Position

The Quality Control Analyst II – Environmental Monitoring supports Environmental Monitoring activities in a GMP-regulated pharmaceutical manufacturing environment. The role provides exposure to manufacturing operations and Quality Control while contributing to laboratory testing, environmental monitoring programs, and quality activities that support safe and reliable production of therapies. The position is onsite in Houston, Texas, Monday through Friday from 8:00 AM to 4:30 PM.

Requirements

Bachelor’s degree in Life Sciences, Biology, Microbiology, Chemistry, or a related scientific discipline.
Strong attention to detail and ability to follow written procedures while maintaining accurate documentation.
Ability to learn technical laboratory processes and environmental monitoring methodologies.
Strong communication and collaboration skills, including the ability to work effectively across multiple departments.
Ability to work in controlled manufacturing environments and adapt to cleanroom requirements.

Nice To Haves

Previous experience in pharmaceutical manufacturing, Environmental Monitoring, Quality Control, or quality-related functions.
Knowledge of GMP-regulated environments and pharmaceutical manufacturing processes.
Experience in aseptic manufacturing, cleanroom operations, or aseptic gowning.

Responsibilities

Perform Environmental Monitoring activities in classified manufacturing and laboratory environments supporting GMP pharmaceutical operations.
Collect and document routine environmental monitoring samples from cleanrooms and controlled manufacturing areas according to approved procedures.
Support laboratory testing and assist with data collection, analysis, and reporting related to environmental monitoring programs.
Follow GMP requirements, standard operating procedures, and site quality standards.
Collaborate with Manufacturing, Quality Control, and other cross-functional teams to align environmental monitoring activities with production schedules and operational goals.
Perform aseptic gowning and work in controlled cleanroom environments while following contamination control practices.
Support batch release activities and quality documentation review as required.
Maintain accurate records and documentation to support regulatory compliance, data integrity, and inspection readiness.