QA Specialist , Compliance

Join our Tampa site as a QA Specialist I, Compliance, where you will support document control and quality systems to ensure compliant GMP operations. This is an exciting opportunity to contribute to quality excellence and patient impact.

• An agile career and dynamic working culture
• An inclusive and ethical workplace
• Compensation programs that recognize high performance
• Medical, dental, and vision insurance
• Opportunities for learning and career growth
• A collaborative and supportive team environment
• Access to global Lonza benefits programs

• Manage document control processes within the Quality Management System
• Review and approve GMP documents in a timely manner
• Maintain document archives and support inspection readiness
• Support internal audits, client audits, and regulatory inspections
• Track and manage document lifecycle activities and logs
• Collaborate with cross‑functional teams to meet project goals
• Support deviation management, investigations, and change control

• Experience in a regulated environment, preferably pharmaceuticals
• Basic knowledge of GMP and FDA regulations
• Familiarity with QMS tools, or willingness to learn
• Strong written and verbal communication skills
• High attention to detail and organizational skills
• Ability to manage multiple tasks and deadlines

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.