QC Specialist III-Stability

Job Title:

QC Specialist III
- Stability

Location:

Portsmouth, NH (On-site)
As a QC Specialist III
- Stability, you will play a critical role in supporting the delivery of life-changing therapies through the management of stability programs in a GMP environment. This is an excellent opportunity to take ownership of stability studies from setup through final reporting while partnering with customers and collaborating across Quality, Program Management, and Operations teams.

This role follows a Monday-Friday, 7:00 AM - 3:30 PM schedule.

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 for career growth and professional developmentA collaborative environment with broad cross-functional exposure

The opportunity to support the delivery of life-changing therapies

What you will do:

Manage stability studies from setup through completion, ensuring quality, compliance, and timely delivery

Partner with customers as a primary stability contact and provide updates throughout the study lifecycle

Develop, review, and maintain stability protocols, reports, and GMP documentation

Coordinate testing activities, sample management, and study timelines with internal and external partners

Collaborate with QC, QA, Program Management, and Operations teams to support customer programs

Support investigations, change controls, and continuous improvement initiatives

Mentor colleagues and contribute to the development of stability best practices across the organization

What we are looking for:

Experience managing stability studies within a GMP-regulated pharmaceutical, biotechnology, or related industry

Strong knowledge of stability protocols, reports, controlled documentation, and quality systems

Ability to build relationships and communicate effectively with customers and cross-functional teams

Experience coordinating multiple priorities and delivering results in a fast-paced environment

Demonstrated problem-solving skills and the ability to work independently

Associate's or Bachelor's degree in Life Sciences or a related field, or equivalent combination of education and experience

Experience in Quality Control, Stability, or other regulated laboratory environments preferred

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.

Summary

Location:

US
- Portsmouth, NHType:
Full time