QC Analyst 2
Lonza
QC Analyst 2
Lonza
Global life sciences contract manufacturer
QC Analyst II-Operations-Night Shift
Location: Portsmouth, NH, USA
Shift: Wednesday through Saturday, 8:00 PM to 6:30 AM on a 4 x 10-hour schedule
Join Lonza's Quality team in Portsmouth, NH, where you will help ensure the quality and safety of products that support life-changing therapies. This is an exciting opportunity to develop your laboratory expertise while contributing to the manufacture of products that make a meaningful difference for patients around the world.
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 professional growth and technical skill development.
Exposure to a collaborative environment across Quality and Manufacturing teams.
The opportunity to contribute to therapies that improve patient lives.
What you will do
Perform testing of raw materials, in-process samples, finished products, and stability samples to support product quality.
Deliver accurate and timely laboratory results to support manufacturing operations and product release.
Review analytical data and documentation to ensure compliance with quality standards.
Document laboratory activities, investigations, and quality records in accordance with established procedures.
Maintain laboratory materials, supplies, and organization to support efficient operations.
Develop knowledge in environmental monitoring, biochemistry, and microbiology testing methods.
Collaborate with Quality, Manufacturing, and technical teams to support continuous improvement and operational excellence.
What we are looking for
Associate's degree in Life Sciences or a combination of education and relevant experience.
Experience working in a regulated laboratory or cGMP environment.
Ability to analyze data and identify trends or issues.
Experience using laboratory systems, quality systems, or related software tools.
Strong organizational skills with the ability to manage multiple priorities.
Effective communication and collaboration skills.
Commitment to quality, safety, continuous learning, and teamwork.
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.
Lonza is a global provider of development and manufacturing services for the pharmaceutical, biotechnology, and nutrition sectors. It supports clients from early development through to commercial production, offering integrated processes such as process development, GMP manufacturing, formulation, fill-finish, and quality assurance to bring medicines and nutrition products to market. Lonza’s model is built on end-to-end CDMO capabilities, enabling companies to move from concept to scalable, compliant production with reliable supply chains. What sets Lonza apart is its long history and global footprint, combining decades of experience across chemistry, biology, and nutrition with a broad, end-to-end service network that supports projects from discovery to commercialization. The company aims to be a trusted, long-term partner in life sciences by helping customers efficiently develop and manufacture their products at scale while maintaining strict regulatory and quality standards.
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