QC Stability Coordinator
Confirmed on the employer's own hiring board on Oct 27, 2026. First seen by Alion on Oct 16, 2026. Randstad Sourceright scores B on the Alion truth index.
Location: Tampa, FL (on-site)
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.
- The full list of our global benefits can be also found on https://www.lonza.com/careers/benefits
- You will coordinate and manage stability studies, including protocols, sample pulls, and storage conditions.
- You will monitor stability data, identify trends, and escalate 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.
- 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 characteristic protected by law.