QC Supervisor, Environmental Monitoring
(3rd shift: 1130p-730a)
Location: Houston, Texas – Onsite
The purpose of the QC Supervisor, Environmental Monitoring role is to lead the QC Microbiology team which is responsible for environmental monitoring (routine and production), utility monitoring, and microbiology testing such as gram stain. In this role you will be responsible for oversight of the environmental monitoring (EM) program including establishment of sampling plans, routine trending, and excursion response procedures in accordance with applicable regulatory guidelines and Lonza policy.
What you will get:
A competitive compensation. 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
Lead, coordinate, and perform Environmental Monitoring activities to support commercial GMP manufacturing in both At Rest and In Operation conditions.
Oversee Microbiology department assays, epidemiological investigations, excursion reports, and laboratory upkeep.
Prepare and maintain SOPs, execute environmental investigations, review/author trend reports, and ensure data integrity.
Ensure all departmental activities comply with corporate policies, cGMPs, and regulatory requirements, including review of data and assay documentation.
Represent QC during audits and client engagements, coordinating cross‑functional communication with manufacturing and other key departments.
Mentor, coach, and develop team members; conduct routine 1:1s, set performance expectations, and manage team and individual goals aligned with site strategy.
Oversee administrative responsibilities such as timesheet approvals and scheduling, ensuring efficient operational support.
What we are looking for
Bachelor’s degree in a scientific discipline or equivalent experience.
Advanced experience in Quality Control within a GMP-regulated environment.
Demonstrated expertise in microbiological assays, microbial identification, environmental monitoring, aseptic processing, and relevant regulatory guidance.
Strong problem‑solving capabilities with the ability to interpret complex data, lead investigations, and implement effective solutions.
Experience managing complex tasks, planning team activities, and ensuring alignment with department goals.
Proficiency in spreadsheets, databases, and word‑processing tools; knowledge of SAP, MODA, and TrackWise is a plus.
Strong communication and leadership skills, including conflict mediation, delivering constructive feedback, and building trust with customers and cross-functional partners.
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 help turn our customers’ breakthrough ideas into viable therapies, we look forward to welcoming you on board.
Ready to shape the future of life sciences? Apply now.
