Lonza
QCStabilityCoordinator
Neural analysis suggests this role is
optimal for Mid+ candidates.
“QC Stability Coordinator at Lonza. Skills: Stability studies, Data monitoring, Quality records. Coordinate and manage stability studies. Monitor stability data”
What You'll Achieve.
ensure product quality and compliance; enhance efficiency, compliance, and data reliability
Industry & Context.
analytical skills with the ability to interpret data and identify trends
What They're Looking For.
Must Have
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, 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
Nice to Have
Familiarity with data tools (e. g. , Excel) and quality systems is preferred
What You'll Do.
Coordinate and manage stability studies
Monitor stability data
Manage quality records
Maintain stability databases
Drive process improvements
How You'll Work.
Team & Collaboration
Collaborate with Quality Control, Quality Assurance, and Product Development teams
Communication Scope
Effective communication skills with both technical and non-technical stakeholders
Full Job Description
# **QC Stability Coordinator** **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 ## **What you will do** * 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. ## **What we are looking for** * Associate degree or higher in a scientific or
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