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 supporting laboratory testing, environmental monitoring programs, and quality activities that contribute to the safe and reliable production of therapies. The position is onsite in Houston, Texas, with a Monday-through-Friday schedule 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 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; experience is preferred but not required.
• Knowledge of GMP-regulated environments and pharmaceutical manufacturing processes.
• Experience in aseptic manufacturing, cleanroom operations, or aseptic gowning.
• Interest in building a long-term career in the pharmaceutical manufacturing industry.

Responsibilities

• Perform Environmental Monitoring activities in classified manufacturing and laboratory environments in support of 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 for environmental monitoring programs.
• Follow GMP requirements, standard operating procedures, and site quality standards in daily activities.
• Collaborate with Manufacturing, Quality Control, and other cross-functional teams to support 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.

Benefits

• Performance-related bonus
• Medical, dental, and vision insurance
• 401(k) matching plan
• Life insurance
• Short-term and long-term disability insurance
• Employee assistance programs
• Paid time off (PTO)

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level