Quality Control Analyst I – Microbial Control

Lonza•Portsmouth, NH

8d•Onsite

About The Position

As a QC Analyst in Microbial Control at Lonza’s Portsmouth site, you will support testing of in-process and final product samples to help ensure the safety and quality of drug products. You will perform microbiological testing, support environmental and utility monitoring, and provide accurate results to meet manufacturing timelines. The role involves hands-on laboratory work and collaboration to maintain quality and compliance with cGMP standards. It is an onsite night-shift position following a Sunday–Wednesday schedule, with working hours from 7:30 PM to 5:30 AM.

Requirements

Associate’s degree in Microbiology, Biochemistry, or a related science field.
Ability to interpret data and identify trends or deviations.
Strong written and verbal communication skills.
Attention to detail and strong organizational skills.
Comfort working in cleanroom environments, including performing physical tasks such as climbing ladders when needed.

Nice To Haves

Experience in a GMP or regulated laboratory environment.
Prior laboratory experience, familiarity with aseptic techniques, and strong documentation practices.

Responsibilities

Perform microbiological testing for in-process, release, and stability samples.
Support environmental and utility monitoring, including HVAC and facility sampling.
Review and document test results in accordance with GMP and data integrity standards.
Use laboratory systems and software to record and manage data.
Identify deviations and support investigations when results fall outside expected ranges.
Ensure compliance with cGMP, GDP, and data integrity requirements in all tasks.
Participate in routine laboratory activities, including sample handling and documentation.