QC Analyst II - Analytical (Night Shift)
Lonza
Summary
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.
Job description
QC Analyst II-Operations-Night Shift
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 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.
Requirements
- 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.
Benefits
- Medical, Dental & Vision
- Professional growth opportunities
- Technical skill development
Company overview
Lonza is a pioneering global Contract Development and Manufacturing Organization (CDMO) and a world leader in pharmaceutical manufacturing services. Founded in 1897 in Switzerland, the company has evolved into the first and original CDMO, now operating as one of the largest Western CDMO networks with approximately 19,000 employees across more than 30 sites spanning five continents. Lonza specializes in transforming therapeutic discoveries into life-saving and life-enhancing treatments for patients worldwide. The company's comprehensive services span from early development to drug substance and drug product manufacturing, covering established and emerging technologies including mammalian biologics, small molecules, highly potent APIs, bioconjugates, mRNA, microbial products, and cell and gene therapies. With a focus on cutting-edge science, smart technology, and lean manufacturing, Lonza serves a diverse customer base ranging from emerging biotechs to global pharmaceutical companies, delivering integrated solutions throughout the entire treatment lifecycle.