Quality Control Analyst II - Night

Lonza Group; Portsmouth (NH); On-site; USD 65,000 - 90,000; Full time

Benefits offered by this job

Medical, dental, and vision insurance

Opportunities for professional growth

Collaborative, ethical workplace

Competitive compensation and benefits

Job summary

Lonza in Portsmouth, NH is seeking a QC Analyst II – Operations (Night Shift) to join the Quality team. You will perform testing on materials and finished products, deliver timely results, and ensure compliance with quality standards in a cGMP environment.

This role supports manufacturing operations and product releases on a 5x8-hour night schedule. Ideal candidates have an Associate's degree in Life Sciences, experience with lab systems, and strong data analysis, organization, and teamwork

Qualifications

• Associate's degree in Life Sciences or an equivalent combination of education and experience.
• Experience 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.

Responsibilities

• 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.

Skills

Data analysis

Communication

Organization

Collaboration

Education

Associate's degree in Life Sciences

Tools

Laboratory systems

Job description

United States, Portsmouth (New Hampshire)

QC Analyst II – Operations (Night Shift)

Location: Portsmouth, NH, USA

Shift: Monday - Friday, 11:00 PM to 7:30 AM on a 5x8-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.

• Take ownership, step forward, and enjoy meaningful responsibility
• Love solving problems and thrive in a complex, fast-moving environment
• Are curious, always looking to learn and improve
• Work collaboratively, contributing to something bigger than yourself
• Are motivated to make a difference through work that impacts customers and their patients

Why Lonza:

We are a place of unique opportunity, where your ideas, expertise and ambition can make a real difference. Here, will have the freedom to grow, the support to succeed and the chance to contribute to work that matters.

We are the makers of the medicines of tomorrow.