Quality Control Analyst II, Microbiology, Commercial

Lonza•Houston, TX

22h•Onsite

About The Position

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. 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.

Requirements

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.
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.

Responsibilities

Perform routine and specialized environmental monitoring in Grade B cleanrooms, requiring Level 3 gowning and extended periods within controlled environments (approximately 65% of role).
Support performance qualifications of cleanrooms 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.
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.