QC Analyst 2 – Microbial Control
Lonza
QC Analyst 2 – Microbial Control
Lonza
Global life sciences contract manufacturer
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 6:00 AM.
What you will get
What you will do
What we are looking for
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.
Lonza is a global provider of development and manufacturing services for the pharmaceutical, biotechnology, and nutrition sectors. It supports clients from early development through to commercial production, offering integrated processes such as process development, GMP manufacturing, formulation, fill-finish, and quality assurance to bring medicines and nutrition products to market. Lonza’s model is built on end-to-end CDMO capabilities, enabling companies to move from concept to scalable, compliant production with reliable supply chains. What sets Lonza apart is its long history and global footprint, combining decades of experience across chemistry, biology, and nutrition with a broad, end-to-end service network that supports projects from discovery to commercialization. The company aims to be a trusted, long-term partner in life sciences by helping customers efficiently develop and manufacture their products at scale while maintaining strict regulatory and quality standards.
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