Lonza

QC Analyst III - Microbiology

Posted Jan 12, 2026
Job ID: R72854
Location
Portsmouth, NH
Hours/week
40 hrs/week
Payrate range
Unknown

Today, 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.

This role supports in-process, lot release, and stability testing for customer drug products while providing technical expertise, training, and project leadership within the Quality Control Microbiology team. The Analyst III delivers high-quality, on-time results to meet Manufacturing demands and drives continuous improvement in a cGMP environment.

What you will get:

● An agile career and dynamic working culture
● An inclusive and ethical workplace
● Compensation programs that recognize high performance
● Medical, dental and vision insurance

Our full list of global benefits can be found here: https://www.lonza.com/careers/benefits.

What you will do:

● Perform microbial testing in support of in-process, lot release, and customer stability studies
● Support utility, environmental, and HVAC monitoring and sampling throughout the facility
● Review assays, test data, and documentation, identifying deviations and ensuring compliance with procedures
● Author quality records and documentation, including deviations, CAPAs, change controls, and test methods
● Train and mentor other analysts, supporting skill development and consistent laboratory execution
● Lead and support projects such as method transfers, new instrument implementation, and method qualification activities
● Apply cGMP and Data Integrity principles in all aspects of work in accordance with Lonza policies and procedures

What we are looking for:

● Experience performing microbiology testing in a cGMP-regulated Quality Control laboratory
● Demonstrated ability to recognize deviations from accepted practices and evaluate data of moderate complexity
● Experience with quality systems and laboratory platforms such as LIMS and TrackWise
● Strong written and verbal communication skills, including the ability to present information and train others
● Proven ability to plan, prioritize, and lead tasks or projects within defined timelines
● Proficiency with Microsoft Office and laboratory computer systems
● Self-motivated team player with strong judgment, accountability, and commitment to quality

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.

Ready to shape the future of life sciences? Apply now.

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