QC Stability Coordinator

LonzaTampa, FL
Onsite

About The Position

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.

Requirements

  • 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.

Nice To Haves

  • Familiarity with data tools (e.g., Excel) and quality systems is preferred.

Responsibilities

  • Coordinate and manage stability studies, including protocols, sample pulls, and storage conditions.
  • Monitor stability data, identify trends, and escalate 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.

Benefits

  • 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.
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