Quality Control Analyst II, Microbiology, Commercial

Overview

Quality Control Analyst ll, Microbiology, Commercial

Shift: 2nd shift - Wednesday to Saturday (4x10)

Location: Houston, TX – Onsite

Join our dynamic Quality Control Microbiology team in Houston, where you’ll play a critical role in maintaining compliant cleanroom environments and ensuring the successful manufacture of life‑changing therapies. This position offers hands-on work in a fast-paced GMP facility and the opportunity to grow your microbiology and aseptic processing skills.

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.

• Perform routine and specialized environmental monitoring in Grade B clean rooms, requiring Level 3 gowning and extended periods within controlled environments (approximately 65% of role).
• Support performance qualifications of clean rooms during initial and ongoing manufacturing activities.
• Execute microbiological assays for media and product release; coordinate microorganism identifications and maintain laboratory supplies and equipment.
• Write and contribute to investigations, excursion reports, SOPs, trend reports, deviations, and CAPAs
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• Participate in environmental investigations and help drive continuous improvement within the microbiology team.
• Ensure strict adherence to cGMP requirements and report any regulatory or quality concerns in a timely manner.
• Perform additional assigned duties while promoting a safe, compliant, and efficient working environment.

• Bachelor’s degree in a biological science or related field preferred.

• Relevant experience in microbiology, environmental monitoring, or laboratory operations.

• Demonstrated knowledge of microbiological assays, aseptic processing, and general laboratory techniques
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• Understanding of cGMP requirements within a manufacturing or QC environment.

• Strong written and verbal communication skills, along with proficiency in Microsoft Word and Excel.

• Excellent organizational skills with the ability to prioritize, follow through on tasks, and meet deadlines.

• A proactive, collaborative, and responsible mindset with strong interpersonal skills and a can‑do attitude
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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.

Apply now.