Stability QC Coordinator – Data-Driven Quality & Compliance

Lonza; Tampa (FL); On-site; Confidential; Full time

Benefits offered by this job

Agile culture

Inclusive workplace

Performance-based pay

Health insurance

Meaningful work

Career development

Job summary

Lonza in Tampa, FL is seeking a QC Stability Coordinator to manage stability studies across development and commercial stages. The role emphasizes GMP compliance, data integrity, and cross-functional collaboration to ensure product quality.

You will coordinate protocols, monitor trends, support audits, and maintain stability records while driving improvements for efficiency and reliability within the stability program.

Qualifications

• Associate degree or higher in a scientific or related discipline.
• Experience in a regulated environment (pharma/biotech/lab).
• Knowledge of GMP and stability program requirements.
• Strong analytical skills to interpret data and identify trends.
• Ability to manage multiple priorities across teams.
• Effective communication with technical and non-technical stakeholders.
• Familiarity with data tools 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

Multi-tasking

Communication skills

Education

Associate degree in science

Tools

Excel

Job description

Lonza in Tampa, FL is seeking a QC Stability Coordinator to manage stability studies across development and commercial stages. The role emphasizes GMP compliance, data integrity, and cross-functional collaboration to ensure product quality.

You will coordinate protocols, monitor trends, support audits, and maintain stability records while driving improvements for efficiency and reliability within the stability program.