QC Analyst II-Microbial Control
@ US02 Lonza Biologics Inc.QC Analyst II-Microbial Control
About the job
Lonza is a global leader in life sciences manufacturing. This QC Analyst II role focuses on microbiological testing, environmental monitoring, and ensuring compliance with cGMP standards at our Portsmouth site. The work involves hands-on lab tasks, collaboration, and supporting quality and safety in drug production.
Requirements
- Associate’s degree in Microbiology or related
- Experience in GMP or regulated lab
- Data interpretation skills
- Strong communication skills
- Attention to detail
Qualifications
- Laboratory experience preferred
- Aseptic techniques knowledge
- Comfortable in cleanroom environments
- Physical ability for lab tasks
Full job description
Job Title: Quality Control Analyst II – Microbial Control (Night)
Location: Portsmouth, NH, (On-site)
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.
This position follows a Sunday–Wednesday schedule, with working hours from 7:30 PM to 5:30 AM.
What you will get
Competitive pay and performance-based compensation
Medical, dental, and vision insurance
A supportive and inclusive work environment
Opportunities for career growth and development
Hands-on training and skill-building
A collaborative and team-focused laboratory environment
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
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.
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