Senior QC Analyst
LonzaPortsmouth, New Hampshire, United States
Posted March 6, 2026
Full Time
About the Company
Lonza is a pioneer and world leader in the CDMO industry, setting the pace with cutting-edge science, smart technology, and lean manufacturing. United by a common purpose, we turn our customers’ breakthrough innovations into viable therapies and manufacture the medicines of tomorrow. Founded in Switzerland in 1897, our company is the first and original CDMO, and today we are more dynamic, agile and forward-focused than ever before. As one of the largest Western CDMOs, we bring together a global team of around 18,500 colleagues across five continents to deliver comprehensive, integrated solutions for our customers' complex needs. For our customers and their patients, we bring quality, safety and reliability to bring life-enhancing and life-saving treatments to market at speed and at scale. For our colleagues, we strive to create a sense of belonging and inclusion where every person can thrive and bring their best.
Job Description
The Sr. QC Microbial Analyst supports drug production by performing quality testing on in-process and final product lots, as well as ongoing stability studies.
Requirements
- Bachelor's or Associate's Degree in Microbiology, Biochemistry, or related science discipline
- 5-10 years of GMP industry experience; aseptic experience is preferred
- Use of Microsoft Suites (Word, Excel, PowerPoint) and Laboratory computer systems
- Experience using GMP Quality Systems such as: TrackWise, LIMS preferred
Benefits
- Competitive salary
- Comprehensive benefits package
- Opportunities for career development and advancement
- Supportive and collaborative team environment
- Access to cutting-edge technology and tools
- Commitment to employee well-being and safety
- Inclusive workplace culture
- Recognition and reward for your contributions