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 s…
Skills: Stability Program Management, GMP Knowledge, Data Analysis, Quality Control, Quality Assurance
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Lonza ist heute ein weltweit führendes Unternehmen im Bereich Life Sciences, welches auf drei Kontinenten tätig ist. Wir sind in der Wissenschaft tätig, jedoch gibt es keine Zauberformel dafür, wie wir die Arbeit angehen…
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Lonza ist heute ein weltweit führendes Unternehmen im Bereich Life Sciences, welches auf drei Kontinenten tätig ist. Wir sind in der Wissenschaft tätig, jedoch gibt es keine Zauberformel dafür, wie wir die Arbeit angehen…
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Full-time
associate degree
Medical Insurance, Dental Insurance, Vision Insurance, Compensation Programs, Career Development
Posted 27d ago
~40 hrs/week
Responsibilities
Coordinate and manage stability studies, including protocols, sample pulls, and storage conditions. Monitor stability data to identify trends and manage quality records such as deviations and CAPAs.
Requirements
Requires an associate degree or higher in a scientific discipline and experience in a regulated pharmaceutical or biotech environment. Must have knowledge of GMP and stability program requirements with strong analytical skills.
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.
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 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.
Lonza is a pioneer and world leader in the CDMO industry, setting the pace with cutting-edge science, smart technology, and lean manufacturing. United by a common purpose, we turn our customers’ breakthrough innovations into viable therapies and manufacture the medicines of tomorrow.
Founded in Switzerland in 1897, our company is the first and original CDMO, and today we are more dynamic, agile and forward-focused than ever before. As one of the largest Western CDMOs, we bring together a global team of around 18,500 colleagues across five continents to deliver comprehensive, integrated solutions for our customers' complex needs.
For our customers and their patients, we bring quality, safety and reliability to bring life-enhancing and life-saving treatments to market at speed and at scale. For our colleagues, we strive to create a sense of belonging and inclusion where every person can thrive and bring their best.
Lonza is a pioneer and world leader in the CDMO industry, setting the pace with cutting-edge science, smart technology, and lean manufacturing. United by a common purpose, we turn our customers’ breakthrough innovations into viable therapies and manufacture the medicines of tomorrow.
Founded in Switzerland in 1897, our company is the first and original CDMO, and today we are more dynamic, agile and forward-focused than ever before. As one of the largest Western CDMOs, we bring together a global team of around 18,500 colleagues across five continents to deliver comprehensive, integrated solutions for our customers' complex needs.
For our customers and their patients, we bring quality, safety and reliability to bring life-enhancing and life-saving treatments to market at speed and at scale. For our colleagues, we strive to create a sense of belonging and inclusion where every person can thrive and bring their best.