QC Analyst 2, Microbiology (Biotech)
oday, Lonza is a global leader in life sciences operating across five continents. While we work in science, there's no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that's the kind of work we want to be part of.
Lonza AG is excited to present an outstanding opportunity for a Quality Control Analyst I, Microbiology, based in New Hampshire, USA! The Quality Control Analyst I will act as a team member of the Quality Control Microbiology department to support production of in-process and final product drug lots for customer(s)! Participate in sample collection and testing for ongoing customer stability studies and provide timely, high-quality results to meet Manufacturing demands.
For training purposes, start of hire schedule will be Mon-Fri from date of onboarding to approximately the end of December 2025. From then on the posted 4/10 schedule will be implemented. Additional temporary adjustments in schedules may be required to meet business needs in early 2026.
Key responsibilities:
Running test samples for In-Process, Lot Release, and Stability studies.
Supporting Utility and HVAC supervising and sampling throughout the facility.
Reviewing assays to resolve accuracy and compliance with established standards.
Applying Microsoft Software (Word, Excel, PowerPoint) for compiling and analyzing data.
Applying knowledge of GMP Quality Systems such as TrackWise and LIMS.
Using Laboratory computer systems to support testing and analysis.
Working on semi-routine assignments, recognizing and addressing deviations from accepted practices.
Analyzing situations or data to identify factors and determine solutions for moderate scope problems.
Applying Data Integrity principles in all aspects of work, closely adhering to Lonza's Data Integrity policies, guidelines, and procedures.
Performing other duties as assigned to support the overall goals of the department.
Leading projects like onboarding new equipment and participating in Lean Six Sigma initiatives.
Key requirements:
Associate Degree or equivalent experience in a related field.
2-4 years of proven experience in a similar role, demonstrating a track record of successful implementation of testing and quality control processes.
Outstanding analytical skills with the ability to challenge in a fast-paced environment.
Strong familiarity with GMP Quality Systems and laboratory computer systems.
Ability to work collaboratively within a team and independently, showing ambition and initiative.
Proven experience with Microsoft Software, including Word, Excel, and PowerPoint.
Excellent problem-solving skills and attention to detail.
Join us at Lonza AG, where your contributions will be valued, and your career path is yours to determine. Apply today to be a part of our journey toward scientific excellence and making a meaningful impact on the world.
Every day, Lonza's products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.
People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.
Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.
