QC Analyst III - Microbiology

Lonza•Portsmouth, NH

About The Position

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.

Requirements

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

Responsibilities

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