QC Analyst II-Microbial Control
Lonza
Summary
As a QC Analyst II in Microbial Control at our Portsmouth site, you will support the testing of in-process and final product samples to ensure the safety and quality of drug products. You will perform microbiological testing, support environmental and utility monitoring, and deliver accurate results to meet manufacturing timelines. This role is based onsite, where hands-on laboratory work and collaboration are essential to maintaining quality and compliance with cGMP standards.
Job description
This position follows a Monday–Friday schedule, with working hours from 11:00 AM to 7:30 PM.
What you will do
- 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 lab activities, including sample handling and documentation
What we are looking for
- Associate’s degree in Microbiology, Biochemistry, or a related science field
- Experience in a GMP or regulated laboratory environment preferred
- Ability to interpret data and identify trends or deviations
- Strong written and verbal communication skills
- Attention to detail and strong organizational skills
- Prior laboratory experience, familiar with aseptic techniques and strong documentation practices, preferred
- Comfortable working in cleanroom environments, including performing physical tasks such as climbing ladders when needed
Requirements
- Associate’s degree in Microbiology, Biochemistry, or a related science field
- Experience in a GMP or regulated laboratory environment preferred
- Ability to interpret data and identify trends or deviations
- Strong written and verbal communication skills
- Attention to detail and strong organizational skills
- Prior laboratory experience, familiar with aseptic techniques and strong documentation practices, preferred
- Comfortable working in cleanroom environments, including performing physical tasks such as climbing ladders when needed
Benefits
- Competitive pay
- Performance-based compensation
- Medical, Dental & Vision
- Career growth opportunities
- Hands-on training
- Collaborative work environment
Company overview
Lonza is a pioneering global Contract Development and Manufacturing Organization (CDMO) and a world leader in pharmaceutical manufacturing services. Founded in 1897 in Switzerland, the company has evolved into the first and original CDMO, now operating as one of the largest Western CDMO networks with approximately 19,000 employees across more than 30 sites spanning five continents. Lonza specializes in transforming therapeutic discoveries into life-saving and life-enhancing treatments for patients worldwide. The company's comprehensive services span from early development to drug substance and drug product manufacturing, covering established and emerging technologies including mammalian biologics, small molecules, highly potent APIs, bioconjugates, mRNA, microbial products, and cell and gene therapies. With a focus on cutting-edge science, smart technology, and lean manufacturing, Lonza serves a diverse customer base ranging from emerging biotechs to global pharmaceutical companies, delivering integrated solutions throughout the entire treatment lifecycle.