Quality Control Analyst II - Environmental Monitoring

Lonza; Houston (TX); On-site; Confidential; Full time

Benefits offered by this job

Performance-related bonus

Medical, dental and vision insurance

401(k) matching plan

Life insurance

Short-term and long-term disability 보험

Job summary

Lonza in Houston is seeking a Quality Control Analyst II - Environmental Monitoring to support GMP environmental monitoring in manufacturing and lab environments. The role offers exposure to both production and QC functions, with duties spanning sample collection, data analysis, and documentation.

You will collaborate with cross-functional teams, perform aseptic gowning in cleanrooms, and contribute to batch release activities while maintaining rigorous quality records and regulatory readiness.

Qualifications

• Bachelor's degree in Life Sciences, Biology, Microbiology, Chemistry, or a related scientific discipline.
• Previous experience in pharmaceutical manufacturing, Environmental Monitoring, Quality Control, or quality-related functions preferred but not required.
• Knowledge of GMP-regulated environments and pharmaceutical manufacturing processes preferred.
• Experience in aseptic manufacturing, cleanroom operations, or aseptic gowning is highly desirable.
• Strong attention to detail and ability to follow written procedures while maintaining accurate documentation.
• Demonstrated ability to learn technical laboratory processes and environmental monitoring methodologies.

Responsibilities

• Perform Environmental Monitoring activities within classified manufacturing and laboratory environments in support of GMP pharmaceutical operations.
• Collect and document routine environmental monitoring samples from cleanrooms and controlled manufacturing areas following approved procedures.
• Support laboratory testing activities and assist with data collection, analysis, and reporting related to environmental monitoring programs.
• Maintain compliance with GMP requirements, standard operating procedures, and site quality standards while performing daily activities.
• Collaborate with Manufacturing, Quality Control, and other cross-functional teams to ensure environmental monitoring activities support production schedules and operational goals.
• Perform aseptic gowning and work within controlled cleanroom environments while adhering to 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.

Skills

Environmental Monitoring

GMP Knowledge

Documentation

Cross-functional Collaboration

Education

Bachelor's degree in Life Sciences

Tools

LIMS

MS Office

Job description

Quality Control Analyst II - Environmental Monitoring

Location: Houston, Texas - Onsite

Shift: Monday through Friday, 8:00 AM - 4:30 PM

As a Quality Control Analyst II - Environmental Monitoring , you will play a critical role in supporting Environmental Monitoring activities within a GMP-regulated pharmaceutical manufacturing environment. This position offers a unique opportunity to gain exposure to both manufacturing operations and Quality Control functions while supporting laboratory testing, environmental monitoring programs, and quality activities that contribute to the safe and reliable production of life-changing therapies.

What you will get:

A competitive compensation package. In addition, below you will find a comprehensive summary of the benefits package we offer:

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

Compensation for this role will be determined by the candidate's qualifications, skills, experience, and relevant knowledge.

What you will do:

• Perform Environmental Monitoring activities within classified manufacturing and laboratory environments in support of GMP pharmaceutical operations.
• Collect and document routine environmental monitoring samples from cleanrooms and controlled manufacturing areas following approved procedures.
• Support laboratory testing activities and assist with data collection, analysis, and reporting related to environmental monitoring programs.
• Maintain compliance with GMP requirements, standard operating procedures, and site quality standards while performing daily activities.
• Collaborate with Manufacturing, Quality Control, and other cross-functional teams to ensure environmental monitoring activities support production schedules and operational goals.
• Perform aseptic gowning and work within controlled cleanroom environments while adhering to 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.

What we are looking for:

• Bachelor's degree in Life Sciences, Biology, Microbiology, Chemistry, or a related scientific discipline.
• Previous experience in pharmaceutical manufacturing, Environmental Monitoring, Quality Control, or quality-related functions preferred but not required.
• Knowledge of GMP-regulated environments and pharmaceutical manufacturing processes preferred.
• Experience in aseptic manufacturing, cleanroom operations, or aseptic gowning is highly desirable.
• Strong attention to detail and ability to follow written procedures while maintaining accurate documentation.
• Demonstrated ability to learn technical laboratory processes and environmental monitoring methodologies.
• Strong communication and collaboration skills with the ability to work effectively across multiple departments.
• Ability to work in controlled manufacturing environments and adapt to cleanroom requirements.
• Motivated early-career professionals seeking to build a long-term career in the pharmaceutical manufacturing industry are encouraged to apply.

About Lonza

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

Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we offer equal employment opportunities to all qualified applicants regardless of race, religion, color, national origin, sex, sexual orientation, gender identity, age, disability, veteran status, or any other characteristic protected by law.

If you're ready to launch your career in pharmaceutical manufacturing while contributing to the development of life-changing therapies, we look forward to welcoming you on board.