QC Stability Coordinator

Lonza; Tampa (FL); On-site; USD 70,000 - 90,000; Full time

Benefits offered by this job

Medical, dental and vision insurance

Career development

Inclusive workplace

Agile culture

Job summary

Lonza in Tampa seeks a QC Stability Coordinator to manage stability studies across development, clinical, and commercial stages. You will coordinate protocols, sample pulls, and storage conditions while monitoring data for trends and Ober to stability issues.

You will support audits, manage deviations and change controls, and work with QC/QA/PD teams to design and execute studies. This role emphasizes data reliability and program visibility.

Qualifications

• Associate degree or higher in a scientific field.
• Experience in regulated pharma, biotech, or laboratory settings.
• Knowledge of GMP and stability program requirements.
• Strong analytical skills to interpret data and identify trends.
• Ability to manage multiple priorities and coordinate activities across teams.
• Effective communication with technical and non-technical stakeholders.
• Familiarity with data tools (Excel) and quality systems preferred.

Responsibilities

• Coordinate and manage stability studies, including protocols, sample pulls, and storage conditions.
• Monitor stability data, identify trends, and elevate out-of-specification or out-of-trend results.
• Support audits by preparing documentation and responding to stability-related inquiries.
• Manage quality records such as deviations, CAPAs, and change controls within the stability program.
• Collaborate with Quality Control, Quality Assurance, and Product Development teams to support study design and execution.
• Maintain stability databases, dashboards, and performance metrics to ensure program visibility.
• Drive process improvements to enhance efficiency, compliance, and data reliability.

Skills

Analytical skills

Cross-functional coordination

Effective communication

Excel/data tools

Regulated environment experience

Data interpretation

Education

Associate degree or higher in a scientific field

Tools

Excel

Job description

Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of.

As a QC Stability Coordinator in Tampa, you will play a critical role in managing stability programs that ensure product quality and compliance across development, clinical, and commercial stages.

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 contribute to meaningful work that improves lives.
• Career development through cross-functional collaboration and continuous improvement initiatives.
• You will coordinate and manage stability studies, including protocols, sample pulls, and storage conditions.
• You will monitor stability data, identify trends, and elevate out-of-specification or out-of-trend results.
• You will support audits by preparing documentation and responding to stability-related inquiries.
• You will manage quality records such as deviations, CAPAs, and change controls within the stability program.
• You will collaborate with Quality Control, Quality Assurance, and Product Development teams to support study design and execution.
• You will maintain stability databases, dashboards, and performance metrics to ensure program visibility.
• You will drive process improvements to enhance efficiency, compliance, and data reliability.

What we are looking for

• Associate degree or higher in a scientific or related discipline.
• Experience in a regulated environment such as pharmaceutical, biotech, or laboratory settings.
• Knowledge of GMP and stability program requirements, including regulatory guidelines.
• Strong analytical skills with the ability to interpret data and identify trends.
• Ability to manage multiple priorities and coordinate activities across teams.
• Effective communication skills with both technical and non-technical stakeholders.
• Familiarity with data tools (e.g., Excel) and quality systems is preferred.

Every day, Lonza’s products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.

People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.

Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristically protected by law.

Reference: R79610

You will feel at home at Lonza if you:

• 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.