QC Analyst IV-Immunology

Job Title: Quality Control Analyst IV – Immunology

Location: Portsmouth, NH, (On-site)

At Lonza, a global leader in life sciences, we work together to develop innovative solutions that help improve lives around the world. As a QC Analyst IV, you will play a key role in supporting Quality Control testing for in-process materials, raw materials, environmental monitoring programs, stability studies, and finished products within a cGMP-regulated environment. You will perform advanced laboratory testing, analyze and interpret data, support investigations, and help ensure products meet quality and regulatory requirements. This role provides opportunities to serve as a technical resource, mentor junior analysts, support laboratory initiatives, and drive continuous improvement across the Quality Control organization

The schedule for this position is Monday through Friday, 8:00 AM to 4:30 PM.

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

• Opportunities to grow and develop your career

• A collaborative and team-focused laboratory environment

What you will do

• Perform advanced quality control testing to support manufacturing, stability studies, environmental monitoring, and product release activities

• Analyze and interpret laboratory data, ensuring accurate and timely reporting of results

• Serve as a subject matter expert for laboratory methods, instrumentation, and quality systems

• Troubleshoot laboratory equipment, software, analytical methods, and testing processes

• Support method transfers, implementation of new instrumentation, and continuous improvement initiatives

• Mentor, train, and provide technical guidance to laboratory staff

• Initiate and support deviations, CAPAs, investigations, and change controls using electronic quality systems

• Utilize systems such as TrackWise, LIMS, DMS, and other laboratory platforms to maintain compliance and documentation

• Collaborate with Manufacturing, QA, MSAT, Validation, and other cross-functional teams to support operational needs

• Drive audit readiness activities and support regulatory inspections as a laboratory subject matter expert.

What we are looking for

• Bachelor's degree in Life Sciences or a related scientific field preferred; equivalent combinations of education and experience will be considered

• 5+ years of experience in a GMP-regulated laboratory environment

• Experience performing analytical, biochemical, immunological, microbiological, environmental monitoring, or quality control testing

• Experience with laboratory instrumentation, test methods, troubleshooting, and data analysis

• Experience using electronic laboratory and quality systems such as TrackWise, LIMS, DMS, or similar platforms preferred

• Strong understanding of cGMP regulations, GDP requirements, and data integrity principles

• Demonstrated ability to lead projects, mentor team members, and support investigations

• Strong communication, organization, and problem-solving skills

• Ability to work independently while contributing to a collaborative team environment.

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.